Saturday, June 21, 2025

Saint Tragedy Signs With Rock Sun Records/Virgin Music Group

Saint Tragedy Signs With Rock Sun Records/Virgin Music Group
Vanquish Vol. 2 coming July 25th
New EP Vanquish Vol. 2 Set to Release July 25

Rock Sun Records, in partnership with Virgin Music Group, is proud to announce the newest addition to its expanding roster—Saint Tragedy, the hard-hitting rock outfit hailing from Kenosha, Wisconsin. With a reputation for emotionally-charged live performances and a sound that fuses modern rock grit with classic influence, the band is preparing to unleash their new EP Vanquish Vol. 2 on July 25.

Formed in 2008 by frontman Wayne Wiginton, Saint Tragedy has spent the last decade-plus forging a sound uniquely their own. Blending passion, fire, and a no-holds-barred stage presence, the band—featuring Sid Serbedzija (lead guitar), Eric Serbedzija (bass), and Michael Quinn (drums)—has steadily built a name for themselves in the Midwest and beyond, opening for national acts and cultivating a fiercely loyal fanbase along the way.

The signing marks a pivotal chapter in the band’s journey. “It’s about pure, raw honesty,” says Wiginton. “When we go up there, it’s like you forget about the real world for a moment and just leave it all on the stage.”

Vanquish Vol. 2 is the follow-up to their previous release, continuing the sonic evolution of Saint Tragedy’s sound—one that walks the line between raw emotion and refined musicianship. The EP promises a powerful dose of modern hard rock with heartfelt lyrics and thunderous energy, showcasing the band’s growth while staying true to their roots.

“We couldn’t be more excited to welcome Saint Tragedy to the Rock Sun family,” says Rock Sun founder Tom Hooks. “They represent everything we love about rock music—authenticity, passion, and an undeniable presence on and off the stage.”

With the release of Vanquish Vol. 2 on the horizon and the full force of Rock Sun Records and Virgin Music Group behind them, Saint Tragedy is poised to bring their sound to an even larger audience.

Get ready to feel the fire—Vanquish Vol. 2 arrives July 25. Pre-Save at: http://tunelink.to/llSqE

Media Contact
Company Name: Rock Sun Records
Email:Send Email
Country: United States
Website: https://rocksunrecords.com/

Friday, June 20, 2025

Systemic Lupus Erythematosus Therapeutics Market Size in 7MM is expected to grow at a decent CAGR by 2034, estimates DelveInsight

Systemic Lupus Erythematosus Therapeutics Market Size in 7MM is expected to grow at a decent CAGR by 2034, estimates DelveInsight

DelveInsight's “Systemic Lupus Erythematosus Treatment Market Insights, Epidemiology and Market Forecast – 2034” report delivers an in-depth understanding of Systemic Lupus Erythematosus, historical and forecasted epidemiology as well as the Systemic Lupus Erythematosus market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.

To know in detail about the Systemic Lupus Erythematosus Market Outlook, drug uptake, treatment scenario, and epidemiology trends, click here @ Systemic Lupus Erythematosus Treatment Market Size

Key Takeaways from the Systemic Lupus Erythematosus Market Report

  • In June 2025, UCB Biopharma SRL announced a study is to evaluate the ability of dapirolizumab pegol (DZP) as an add-on treatment to standard of care (SOC) medication to achieve clinically relevant long term improvement of moderate to severe disease activity.
  • In June 2025, Novartis Pharmaceuticals conducted a study is to evaluate long-term safety and tolerability of ianalumab in participants with systemic lupus erythematosus who have previously completed the treatment period in one of the two SIRIUS-SLE core studies (CVAY736F12301 or CVAY736F12302).
  • In June 2025, AstraZeneca conducted a study to evaluate the efficacy and safety of a subcutaneous treatment regimen of anifrolumab versus placebo in participants with moderately to severely active, autoantibody-positive systemic lupus erythematosus (SLE) while receiving standard of care (SOC) treatment. Participants must be taking either 1 or any combination of the following: oral glucocorticoids, antimalarial, and/or immunosuppressants. The study will be performed in adult participants of 18 to 70 years of age.
  • In June 2025, Merck Sharp & Dohme LLC organized a study is to evaluate the efficacy and safety of MK-6194 in adult participants with Systemic Lupus Erythematosus. The primary hypothesis is that at least 1 of the MK-6194 arms is superior to placebo in the primary endpoint of percentage of participants with systemic lupus erythematosus responder index (SRI-4) response at Week 28.
  • In June 2025, AbbVie organized a study will assess how safe and effective upadacitinib is in treating adult participants with moderately to severely active SLE. Adverse events and change in the disease activity will be assessed.
  • Between EU4 and the UK, Spain accounted for the highest number of Systemic Lupus Erythematosus Diagnosed Prevalent Cases followed by the UK and Germany.
  • The age group most affected by the systemic lupus erythematosus prevalence is 40-59 years. In 2023, among 7MM, approximately 40% of cases belonged to the 40-59 years age group.
  • In 2023, approximately 50% of cases were found to be moderate cases in Spain.
  • The leading Systemic Lupus Erythematosus Companies such as Biogen, Novartis, MorphoSys, Idorsia Pharmaceuticals, Viatris, RemeGen, UCB Pharma, Genentech, Bristol Myers Squibb, AbbVie and others.
  • Promising Systemic Lupus Erythematosus Pipeline Therapies such as Obexelimab, Telitacicept, DS-7011a, Belimumab (GSK1550188), Sirolimus, Ianalumab, ALPN-101, BMS-986165, JMKX000189, BMS-986165 and others.

Get a Free sample for the Systemic Lupus Erythematosus Therapeutics Market Report @ Systemic Lupus Erythematosus Drugs Market

Systemic Lupus Erythematosus Epidemiology Segmentation in the 7MM

  • Total Diagnosed Prevalent Cases
  • Total Diagnosed Prevalent Cases by Gender
  • Total Diagnosed Prevalent Cases by Age
  • Severity-Based Diagnosed Prevalent Cases
  • Total Treated Cases

Download the report to understand which factors are driving Systemic Lupus Erythematosus Epidemiology trends @ Systemic Lupus Erythematosus Prevalence

Systemic Lupus Erythematosus Marketed Drugs

  • BENLYSTA (belimumab): GlaxoSmithKline

BENLYSTA (belimumab), a B-lymphocyte stimulator (BLyS) specific inhibitor, is a fully human monoclonal antibody that binds to soluble BLyS, which is found to be increased in patients with systemic autoimmune diseases like SLE and lupus nephritis (LN). ABy bding BLyS, BENLYSTA inhibits the prolonged survival of B cells, including autoreactive B cells, and reduces the differentiation of B cells into immunoglobulin-producing plasma cells. BENLYSTA does not bind B cells directly. The US FDA first approved BENLYSTA for the treatment of active systemic lupus erythematosus; it is the first and only approved biologic for both SLE and LN in more than 50 years, including for the pediatric population. It was first approved by the US FDA in 2011.

  • SAPHNELO (anifrolumab): AstraZeneca

SAPHNELO (anifrolumab) is a first in class, fully human monoclonal antibody that binds to subunit 1 of the type I interferon (IFN) receptor, blocking the activity of type I IFN. Type I IFNs, such as IFN-alpha, IFN-beta and IFN-kappa, are cytokines involved in regulating the inflammatory pathways implicated in SLE. The majority of adults with SLE have increased type I IFN signaling, which is associated with increased disease activity and severity. SAPHNELO is approved to treat systemic lupus erythematosus in more than 60 countries worldwide including the US, EU and Japan, with reviews ongoing in other countries.

Systemic Lupus Erythematosus Emerging Drugs

  • Cenerimod: Idorsia Pharmaceuticals/Viatris

Cenerimod is a highly selective sphingosine-1-phosphate receptor 1 (S1P1) receptor modulator, given as an oral once-daily tablet. While the cause of SLE is not fully known, T and B-lymphocytes are considered the key immune cells playing a role in the development of SLE. T and B-lymphocytes have a cell surface receptor called S1P1. These receptors enable T and B-lymphocytes to detect the signaling molecule S1P – sphingosine 1 phosphate – which is responsible for lymphocyte trafficking from the lymph nodes to the circulation. By binding to S1P1 receptors, a receptor modulator can trigger the internalization of those receptors. This effectively blinds T and B lymphocytes to the S1P gradient, thereby holding them in the lymph nodes and reducing autoreactive T and B cells in the circulation and, consequently, also in the tissues. In December 2017, the US FDA designated the investigation of cenerimod for the treatment of SLE as a fast-track development program. Currently it is in Phase III of its clinical development.

  • Litifilimab: Biogen

Litifilimab is a humanized IgG1 monoclonal antibody (mAb) targeting BDCA2 and is being investigated for the potential treatment of SLE and cutaneous lupus erythematosus (CLE). BDCA2 is a receptor that is predominantly expressed on a subset of human immune cells called Plasmacytoid Dendritic Cells (pDCs). The binding of litifilimab to BDCA2 has been shown to reduce the production of pro-inflammatory molecules by pDCs, including type-I interferon (IFN-I) as well as other cytokines and chemokines. Currently it is in Phase III of its clinical development.

Discover more about therapies set to grab major Systemic Lupus Erythematosus Drugs Market Share @ Systemic Lupus Erythematosus Clinical Trials Assessment

Systemic Lupus Erythematosus Treatment Market

Systemic lupus erythematosus is a chronic autoimmune disease that can affect many parts of the body. Lupus occurs when the immune system, which normally helps protect the body from infection and disease, attacks its own tissues. This attack causes inflammation, and in some cases permanent tissue damage, which can be widespread – affecting the skin, joints, heart, lung, kidneys, circulating blood cells, and brain. The systemic lupus erythematosus diagnosis is based on a combination of clinical findings and laboratory evidence. Familiarity with the diagnostic criteria helps clinicians to recognize systemic lupus erythematosus and to subclassify this complex disease based on the pattern of target-organ manifestations. The ACR/EULAR classification requires an antinuclear antibody (ANA) titer of at least 1:80 on HEp-2 cells or an equivalent positive test at least once. If that is present, 22 "additive weighted" classification criteria are considered, comprising seven clinical domains (constitutional, hematologic, neuropsychiatric, mucocutaneous, serosal, musculoskeletal, renal) and three immunologic domains (antiphospholipid antibodies, complement proteins, SLE-specific antibodies). Each criterion is assigned points, ranging from 2 to 10. Patients with at least one clinical criterion and 10 or more points are classified as having systemic lupus erythematosus.

Scope of the Systemic Lupus Erythematosus Market Report

  • Coverage- 7MM
  • Study Period- 2020-2034
  • Systemic Lupus Erythematosus Companies- Biogen, Novartis, MorphoSys, Idorsia Pharmaceuticals, Viatris, RemeGen, UCB Pharma, Genentech, Bristol Myers Squibb, AbbVie and others.
  • Systemic Lupus Erythematosus Pipeline Therapies- Obexelimab, Telitacicept, DS-7011a, Belimumab (GSK1550188), Sirolimus, Ianalumab, ALPN-101, BMS-986165, JMKX000189, BMS-986165 and others.
  • Systemic Lupus Erythematosus Therapeutic Assessment: Systemic Lupus Erythematosus current marketed and emerging therapies
  • Systemic Lupus Erythematosus Market Dynamics: Systemic Lupus Erythematosus market drivers and Systemic Lupus Erythematosus market barriers
  • Systemic Lupus Erythematosus Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
  • Systemic Lupus Erythematosus Unmet Needs, KOL’s views, Analyst’s views, Systemic Lupus Erythematosus Market Access and Reimbursement

Download DelveInsight’s latest report to gain strategic insights into upcoming Systemic Lupus Erythematosus Therapies and Drugs Developments @ Systemic Lupus Erythematosus Market Drivers and Barriers, and Future Perspectives

Table of Contents

1. Key Insights

2. Report Introduction

3. Executive Summary of Systemic Lupus Erythematosus

4. Epidemiology and Market Forecast Methodology

5. SLE Market Overview at a Glance

6. Systemic Lupus Erythematosus Market Disease Background and Overview

7. Systemic Lupus Erythematosus Epidemiology and Patient Population

8. Systemic Lupus Erythematosus Marketed Therapies

9. Systemic Lupus Erythematosus Emerging Therapies

10. Systemic Lupus Erythematosus (SLE): The 7MM Analysis

11. Systemic Lupus Erythematosus Unmet Needs

12. Systemic Lupus Erythematosus SWOT Analysis

13. Systemic Lupus Erythematosus KOL Views

14. Systemic Lupus Erythematosus Market Access and Reimbursement

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Yash Bhardwaj
Email:Send Email
Phone: 09650213330
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/report-store/systemic-lupus-erythematosus-market

Vitiligo Therapeutics Market Size in 7MM is expected to grow at a decent CAGR by 2034, estimates DelveInsight

Vitiligo Therapeutics Market Size in 7MM is expected to grow at a decent CAGR by 2034, estimates DelveInsight

DelveInsight's “Vitiligo Treatment Market Insights, Epidemiology and Market Forecast – 2034” report delivers an in-depth understanding of Vitiligo, historical and forecasted epidemiology as well as the Vitiligo market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.

To know in detail about the Vitiligo market outlook, drug uptake, treatment scenario, and epidemiology trends, click here @ Vitiligo Treatment Market Size

Key Takeaways from the Vitiligo Market Report

  • In June 2025, Incyte Corporation announced a study to evaluate the safety and efficacy of ruxolitinib cream in pediatric participants with non-segmental vitiligo.
  • In June 2025, Pfizer conducted a study to learn about the safety and effects of the study medicine ritlecitinib for the possible treatment of non-segmental vitiligo. Vitiligo causes white patches on your skin when the cells that give your skin color are destroyed. Nonsegmental means that it can affect both sides of the body, such as both knees and both hands.
  • In June 2025, Vyne Therapeutics Inc. organized a Phase 2b Trial Evaluating the Efficacy, Safety & Pharmacokinetics of VYN201 Gel in the Treatment of Non-Segmental Vitiligo.
  • According to the findings, the United States accounted for around 60% of the Vitiligo diagnosed Prevalent Cases in the 7MM in 2023.
  • In EU4 and the UK, Germany contributed the highest patient share of vitiligo, followed by the UK. Whereas Spain contributed to the lowest patient share.
  • As per the estimates, there were 493,000 treated cases of vitiligo in the 7MM in 2023.
  • The leading Vitiligo Companies such as Incyte, AbbVie, Pfizer, Clinuvel, Inc., Clinuvel Pharmaceuticals, Bioniz Therapeutics, TAGCyx Biotechnologies, Temprian Therapeutics, Aclaris Therapeutics, TWi Biotechnology, Dermavant Sciences, Amgen, Pfizer, Incyte Corporation, and others
  • Promising Vitiligo Pipeline Therapies such as OPZELURA (ruxolitinib cream), RINVOQ (upadacitinib), Ritlecitinib, Afamelanotide, Phimelanotide, BNZ-1, TAGX-0003, TT-01, ATI-1777, AC-1101, Cerdulatinib, AMG 714, Ritlecitinib, Ruxolitinib, and others.

Get a Free sample for the Vitiligo Therapeutics Market Report @ Vitiligo Drugs Market

Vitiligo Epidemiology Segmentation in the 7MM

  • Vitiligo Prevalence Cases
  • Vitiligo Type-specific Cases
  • Vitiligo Diagnosed Prevalent Cases
  • Vitiligo Treated Cases

Download the report to understand which factors are driving Vitiligo epidemiology trends @ Vitiligo Prevalence

Vitiligo Marketed Drugs

  • OPZELURA (ruxolitinib cream): Incyte

In July 2024, the US FDA approved a groundbreaking treatment for vitiligo, a chronic immune-mediated skin disorder characterized by depigmented white patches on the skin. The newly approved drug, OPZELURA, is a topical Janus kinase (JAK) inhibitor called ruxolitinib. This approval marks a significant milestone, as OPZELURA is the first FDA-approved pharmacologic treatment specifically designed to address repigmentation in vitiligo patients, particularly those with nonsegmental vitiligo, the most common form of the condition. OPZELURA works by targeting JAK1 and JAK2 receptors to decrease interferon gamma signaling by immune cells, thereby halting the destruction of melanocytes responsible for skin color.

Vitiligo Emerging Drugs

  • RINVOQ (upadacitinib): Abbvie

Upadacitinib (ABT-494) is a JAK1 selective inhibitor being investigated to treat alopecia areata, ankylosing spondylitis, atopic dermatitis, axial SpA, Crohn's disease, giant cell arteritis, hidradenitis suppurativa (HS), psoriatic arthritis, rheumatoid arthritis, systemic lupus erthematosus (SLE), Takayasu arteritis, ulcerative colitis, and vitiligo. Currently, the drug is in Phase III for the treatment of vitiligo, for which primary completion date is December 2024. At the 2024 AAD Annual Meeting, late-breaking data showed that upadacitinib demonstrated clinically meaningful repigmentation of extensive vitiligo after 52 weeks, potentially offering a new and effective systemic treatment for non-segmental vitiligo.

  • LITFULO (Ritlecitinib): Pfizer

LITFULO (ritlecitinib) is considered a kinase inhibitor, meaning it prevents kinases, which are certain proteins in the immune system, from working properly. This in turn blocks the immune pathways that are thought to contribute to the development of autoimmune diseases, resulting in symptom improvements, such as repigmentation or stopping of disease progression in vitiligo. Currently, there is a Phase III Vitiligo Clinical Trial underway with an estimated completion date in June 2025. Depending on the results of that trial, ritlecitinib may be approved for vitiligo treatment.

Discover more about therapies set to grab major Vitiligo market share @ Vitiligo Clinical Trials Assessment

Vitiligo Treatment Market

The Vitiligo Treatment Market Landscape is undergoing rapid transformation, marked by significant advancements anticipated in 2024 and beyond. With the introduction of FDA-approved topical therapies and the emergence of oral JAK inhibitors, dermatology is experiencing remarkable progress in managing this complex condition. These developments signify a promising future for vitiligo patients, reflecting the evolving strategies aimed at enhancing treatment efficacy and patient outcomes. Key Vitiligo Companies such as AbbVie, Incyte, Pfizer, and others are evaluating their lead candidates in different stages of clinical development, respectively. They aim to investigate their products for the treatment of vitiligo. Vitiligo treatment typically involves a combination approach, incorporating various topical therapies such as steroids, vitamin D analogues, and calcineurin inhibitors. While mono-therapy topicals have shown improvement, the most effective treatment strategy often involves a combination of phototherapy, oral antioxidants, and both oral and topical medications. This multifaceted approach addresses the complex nature of vitiligo and maximizes therapeutic outcomes. Driven by rising awareness and new treatment options, the vitiligo market is poised for steady growth in the coming years.

Vitiligo Drugs and Companies

  • OPZELURA (ruxolitinib cream): Incyte
  • RINVOQ (upadacitinib): AbbVie
  • Ritlecitinib: Pfizer
  • Afamelanotide: Clinuvel, Inc.
  • Phimelanotide - Clinuvel Pharmaceuticals
  • BNZ-1: Bioniz Therapeutics
  • TAGX-0003: TAGCyx Biotechnologies
  • TT-01: Temprian Therapeutics
  • ATI-1777: Aclaris Therapeutics
  • AC-1101: TWi Biotechnology
  • Cerdulatinib: Dermavant Sciences
  • AMG 714: Amgen
  • Ritlecitinib: Pfizer
  • Ruxolitinib: Incyte Corporation

Vitiligo Market Drivers

  • Increasing awareness
  • Demand for novel therapies
  • Large patient pool and better healthcare infrastructure

Vitiligo Market Barriers

  • Patient compliance
  • Chronic nature of the disease and long-term therapy
  • Lack of adequate financial assistance & stringent regulatory procedure

Download DelveInsight’s latest report to gain strategic insights into upcoming Vitiligo Therapies and key Vitiligo Developments @ Vitiligo Market Drivers and Barriers, and Future Perspectives

Scope of the Vitiligo Market Report

  • Coverage- 7MM
  • Study Period- 2020-2034
  • Vitiligo Companies- Incyte, AbbVie, Pfizer, Clinuvel, Inc., Clinuvel Pharmaceuticals, Bioniz Therapeutics, TAGCyx Biotechnologies, Temprian Therapeutics, Aclaris Therapeutics, TWi Biotechnology, Dermavant Sciences, Amgen, Pfizer, Incyte Corporation, and others
  • Vitiligo Pipeline Therapies- OPZELURA (ruxolitinib cream), RINVOQ (upadacitinib), Ritlecitinib, Afamelanotide, Phimelanotide, BNZ-1, TAGX-0003, TT-01, ATI-1777, AC-1101, Cerdulatinib, AMG 714, Ritlecitinib, Ruxolitinib, and others.
  • Vitiligo Therapeutic Assessment: Vitiligo current marketed and emerging therapies
  • Vitiligo Market Dynamics: Vitiligo market drivers and Vitiligo market barriers
  • Vitiligo Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
  • Vitiligo Unmet Needs, KOL’s views, Analyst’s views, Vitiligo Market Access and Reimbursement

Table of Contents

1 Key Insights

2 Vitiligo Market Report Introduction

3 Vitiligo Executive Summary

4 Key Events

5 Vitiligo Epidemiology and Market Forecast Methodology

6 Vitiligo Market Overview at a Glance

7 Disease Background and Overview: Vitiligo

8 Vitiligo Treatment and Management

9 Vitiligo Epidemiology and Patient Population in the 7MM

10 Patient Journey

11 Vitiligo Marketed Therapies

12 Vitiligo Emerging Therapies

13 Vitiligo: Seven Major Market Analysis

14 Vitiligo Unmet Needs

15 Vitiligo SWOT Analysis

16 Vitiligo KOL Views

17 Vitiligo Market Access and Reimbursement

18 Appendix

19 DelveInsight Capabilities

20 Disclaimer

21 About DelveInsight

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Yash Bhardwaj
Email:Send Email
Phone: 09650213330
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/report-store/vitiligo-market

Uveitis Treatment Market Size in the 7MM was ~USD 1,468.66 million in 2022 and is expected to increase by 2034, estimates DelveInsight

Uveitis Treatment Market Size in the 7MM was ~USD 1,468.66 million in 2022 and is expected to increase by 2034, estimates DelveInsight

DelveInsight’s “Uveitis Market Insights, Epidemiology, and Market Forecast – 2034” report delivers an in-depth understanding of uveitis, historical and forecasted epidemiology, as well as the uveitis market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.

Explore the intricate details of the Uveitis Market: Uncover drug uptake, treatment dynamics, and epidemiological trends with our comprehensive Uveitis Market Forecast. Click here to stay ahead in healthcare innovation @ Uveitis Market Size

Key Takeaways from the Uveitis Market Report

  • In June 2025, AbbVie announced a study is to assess adverse events and effectiveness of adalimumab in Chinese participants requiring high-dose corticosteroids with NIIPPU. Adalimumab is a conditionally approved drug in China used to treat participants with NIIPPU. All participants will receive the same treatment. Approximately 87 adult participants will be enrolled at approximately 15 sites in China.
  • As per DelveInsight analysis, in 2022, there were approximately 1,009,025 Uveitis diagnosed prevalent cases in the 7MM.
  • The total number of Uveitis diagnosed prevalent cases in the US was around 378,281 in 2022.
  • The US contributed to the largest Uveitis diagnosed prevalent population, acquiring ~37.5% of the 7MM in 2022. Whereas Spain accounted for the least, with around ~7% of the total population share, respectively, in 2022.
  • In the US, patients diagnosed with noninfectious uveitis (NIU) are higher in number than infectious uveitis (IU). In 2022, there were nearly 344,587 cases of NIU, while IU accounted for around 33,695 cases. These numbers are expected to rise during the forecast period due to the rise of overall uveitis infection in the US.
  • According to DelveInsight estimates, in EU4 and the UK, based on anatomical location highest cases of uveitis were diagnosed in anterior uveitis, while intermediate uveitis has the least cases. In EU4 and the UK, anterior uveitis accounted for approximately 203,439, followed by 84,154 cases in posterior uveitis, 81,773 cases in pan uveitis, and 46,485 in intermediate uveitis in 2022, which are projected to increase during the forecast period.
  • Japan accounted for approximately 214,892 diagnosed prevalent cases of uveitis, out of which nearly 8,039 cases were of HLA-B27-associated uveitis, 17,315 sarcoidosis, 9,894 Behçet’s disease, 8,658 Vogt–Koyanagi–Harada disease, 618 JIA, 309 ankylosing spondylitis, 3,092 tuberculosis, 11,749 herpes, 81,628 idiopathic, and 73,589 others cases in 2022. These uveitis cases are expected to change during the forecast period in Japan (2023–2034).
  • The leading Uveitis Companies such as AbbVie Inc., Novartis AG, Allergan Inc., Bausch & Lomb Incorporated, Santen Pharmaceutical Co. Ltd, Eyegate Pharmaceuticals Inc., Regeneron Pharmaceuticals, Eyepoint pharmaceuticals Inc., Alimera Sciences Inc., and others.
  • Promising Uveitis Therapies such as Brepocitinib 45 mg PO QD, Izokibep, QLETLI, Baricitinib, Adalimumab, and others.

Navigate the complexities of the Uveitis Market: Gain insights into drug trends, treatment scenarios, and epidemiological data through our insightful Uveitis Market Forecast. Click here to get more insights @ Uveitis Treatment Market

Uveitis Epidemiology Segmentation in the 7MM

• Total Diagnosed Prevalent Cases

• Type-specific Diagnosed Prevalent Cases

• Diagnosed Prevalent Cases of Uveitis by Anatomical

• Etiology-specific Diagnosed Prevalent Cases

Delve deep into the Uveitis Market Landscape: Analyze drug adoption, treatment paradigms, and epidemiological shifts in our detailed Uveitis Market Forecast. Click here to shape the future @ Uveitis Prevalence

Uveitis Marketed Drugs

  • XIPERE: Clearside Biomedical/Bausch+Lomb

XIPERE, a triamcinolone acetonide injectable suspension, is the first approved medicine delivery via injection for suprachoroidal use to treat macular edema associated with uveitis in the US. Delivering the medicine to the suprachoroidal space (SCS) allows targeted delivery of the therapy with low levels elsewhere in the eye.

  • YUTIQ/ILUVIEN: EyePoint Pharmaceuticals/Alimera Sciences

YUTIQ is a sterile nonbioerodible intravitreal implant with 0.18 mg fluocinolone acetonide. It releases the drug at an initial rate of 0.25 µg/day in a 36-month sustained-release drug delivery system. YUTIQ contains a corticosteroid and is indicated for treating chronic noninfectious uveitis affecting the posterior segment of the eye. It is preloaded into a single-dose applicator to facilitate the injection of the implant directly into the vitreous. It was approved by the US FDA in October 2018 and launched commercially in February 2019.

Uveitis Emerging Drugs

  • TRS01: Tarsier Pharma

TRS01, a lead product of Tarsier Pharmaceuticals, first in first-in-class topical immune modulator agent. Dazdotuftide (TRS) is a breakthrough platform technology for treating blinding ocular diseases. TRS was developed to ‘re-engineer’ the immune system. The platform approaches inflammatory diseases from within the system. The technology can effectively treat various autoimmune and inflammatory ocular diseases. TRS01 is a polypeptide conjugate with a dual mechanism of action; the investigational agent induces anti-inflammatory macrophages and inhibits the nuclear factor-kB (Nf-kB) signaling pathway by toll-like receptor 4 (TLR4).

  • OCS-02 (licaminlimab): Oculis Pharma

OCS-02 (licaminlimab) is a single-chain antibody fragment (scFv) that binds to and neutralizes the activity of human TNFa, with a dual mechanism of action (MoA), anti-inflammation, and anti-necrosis. Unlike full-length monoclonal antibodies, scFv fragments can penetrate ocular surface tissues when used as eye drops due to the smaller molecule size giving it the potential to become the first approved topical biologic for DED (dry eye disease) (OCS-02 was previously known as LME636).

Unlock insights into the Uveitis Market: discover drug uptake patterns, treatment landscapes, and epidemiological insights with our exclusive Uveitis Market Forecast. Click here @ Uveitis Market Drivers and Barriers

Uveitis Drugs Market Insights

A severe intraocular inflammatory condition of the uveal tract known as uveitis frequently results in vision loss, blindness, and reduced quality of life. With the disease having a variable presentation, diagnosis and management are difficult. Treatment aims at obtaining quiescence of the disease, either by treating the infectious agent or treating the immune condition. The current promising pharmacological classes for uveitis treatment include corticosteroids, immunosuppressants, and biologics. The uveitis drugs market is growing, driven by innovative therapies and increasing global prevalence.

Uveitis Therapies and Companies

• TRS01: Tarsier Pharma

• Licaminlimab (OCS-02): Oculis Pharma

• Vamikibart (RO720220/RG6179): Roche/Eleven Biotherapeutics

• OLUMIANT (baricitinib): Eli Lilly and Company

• EYS606: Eyevensys

• Izokibep: Acelyrin/Affibody Medical

• Brepocitinib: Priovant Therapeutics (Roivant Sciences and Pfizer)

Uveitis Market Outlook

Uveitis is a serious intraocular inflammatory disorder of the uveal tract, often associated with visual impairment, blindness, and decreased quality of life. It often affects patients in their most active and economically productive years. It is the leading cause of preventable blindness worldwide and is a critically underserved disease in terms of treatment. With the disease having a variable presentation, diagnosis and management are difficult. A prompt diagnosis, with the correct diagnostic approach and assessment of appropriate treatment, is extremely important to reduce inflammation and attain complete remission, thereby mitigating or avoiding ocular complications, permanent cumulative damage, and long-term vision loss. Treatment aims at obtaining quiescence of the disease, either by treating the infectious agent or treating the immune condition.

Gain a strategic edge in the Uveitis Market: explore comprehensive drug insights, treatment updates, and epidemiological forecasts in our in-depth Uveitis Market Forecast. Click here to lead in advancements @ Uveitis Clinical Trials Assessment

Scope of the Uveitis Market Report

• Coverage- 7MM

• Uveitis Companies- AbbVie Inc., Novartis AG, Allergan Inc., Bausch & Lomb Incorporated, Santen Pharmaceutical Co., Ltd, Eyegate Pharmaceuticals Inc., Regeneron Pharmaceuticals, Eyepoint Pharmaceuticals Inc., Alimera Sciences Inc., and others.

• Uveitis Therapies- Brepocitinib 45 mg PO QD, Izokibep, QLETLI, Baricitinib, Adalimumab, and others.

• Uveitis Market Dynamics: Uveitis Market Drivers and Uveitis Market Barriers

• Uveitis Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter's five forces, BCG Matrix, Market entry strategies

• Uveitis Unmet Needs, KOL's views, Analyst's views, Uveitis Market Access and Reimbursement

Table of Contents

1. Key Insights

2. Report Introduction

3. Uveitis Market Overview at a Glance

4. Methodology of Uveitis Epidemiology and Market

5. Executive Summary of Uveitis

6. Key Events

7. Disease Background and Overview of Uveitis

8. Patient Journey

9. Epidemiology and Patient Population

10. Marketed Drugs

11. Emerging Drugs

12. Uveitis: Market Analysis

13. Key Opinion Leaders’ Views

14. SWOT Analysis

15. Unmet Needs

16. Market Access and Reimbursement

17. Appendix

18. DelveInsight Capabilities

19. Disclaimer

20. About DelveInsight

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

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Country: United States
Website: https://www.delveinsight.com/report-store/uveitis-market

Obesity Clinical Trials Appears Robust With 80+ Key Pharma Companies Actively Working in the Therapeutics Segment | DelveInsight

Obesity Clinical Trials Appears Robust With 80+ Key Pharma Companies Actively Working in the Therapeutics Segment | DelveInsight

DelveInsight’s, “Obesity Pipeline Insight 2025” report provides comprehensive insights about 80+ companies and 100+ pipeline drugs in Obesity pipeline landscape. It covers the Obesity pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Obesity therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive Obesity pipeline products in this space.

Stay ahead with the latest insights! Download DelveInsight’s comprehensive Obesity Pipeline Report to explore emerging therapies, key Obesity Companies, and future Obesity treatment landscapes @ Obesity Pipeline Outlook Report

Key Takeaways from the Obesity Pipeline Report

  • In June 2025, Carmot Therapeutics Inc. announced a Phase 2 Study to Evaluate the Efficacy, Safety, and Tolerability of Once-Weekly CT-388 Administered Subcutaneously for 48 Weeks to Participants Who Are Overweight or Obese With Type 2 Diabetes Mellitus.
  • In June 2025, Zomagen Biosciences Ltd. conducted a study to understand if taking VTX3232 alone or in combination with semaglutide is safe in participants diagnosed with Obesity. Approximately 160 patients will take VTX3232 Dose A, Placebo, VTX3232 Dose A in combination with semaglutide, or Placebo in combination with semaglutide.
  • In June 2025, Boehringer Ingelheim organized a study is to find out whether a medicine called survodutide (BI 456906) helps people living with obesity disease to lose weight. Participants are divided into 3 groups by chance, like drawing names from a hat. 2 groups get different doses of survodutide and 1 group gets placebo. Placebo looks like survodutide but does not contain any medicine.
  • In June 2025, Novo Nordisk A/S announced a study will look at how well CagriSema helps people living with obesity to lose weight and maintain the weight loss long-term. The study has 2 parts: The first part is called 'the main study' and the second part is called 'the extension study'. In the main study participants will either get CagriSema (a study medicine) or placebo (a dummy medicine that looks like CagriSema but has no active ingredient). Which treatment participants get is decided by chance. Participants are two times more likely to get CagriSema than placebo. If participants get CagriSema in the main study, participants will continue on CagriSema in the extension study.
  • In June 2025, Hanmi Pharmaceutical Company Limited conducted a phase 3 study to evaluate efficacy and safety of HM11260C in adult obesity patients without diabetes mellitus.
  • DelveInsight’s Obesity pipeline report depicts a robust space with 80+ active players working to develop 100+ pipeline therapies for Obesity treatment.
  • The leading Obesity Companies such as Zealand Pharma, Sciwind Biosciences, Genexine, Sirnaomics, Sparrow Pharmaceuticals, Shionogi, Regor Pharmaceuticals, Innovent Biologics, Pfizer, NodThera Limited, Boehringer Ingelheim, Fractyl Health, TransThera, Clearmind Medicine, PegBio, Biolingus, and others.
  • Promising Obesity Therapies such as APHD-012, Bimagrumab, Semaglutide, CT-868, GLY-200, Bremelanotide, and others.

Discover how the Obesity treatment paradigm is evolving. Access DelveInsight’s in-depth Obesity Pipeline Analysis for a closer look at promising breakthroughs @ Obesity Clinical Trials and Studies

Obesity Emerging Drugs

  • Survodutide: Zealand Pharma

Survodutide (BI 456906) is a long-acting glucagon/GLP-1 receptor dual agonist for once-weekly subcutaneous administration that activates two key gut hormone receptors simultaneously and may offer better efficacy than current single-hormone receptor agonist treatments. Survodutide is targeting the treatment of obesity and nonalcoholic steatohepatitis (NASH). Boehringer Ingelheim is advancing survodutide into three global Phase III trials in people living with overweight or obesity.

  • Ecnoglutide: Sciwind Biosciences

Glucagon-like peptide-1 (GLP-1) analogs are effective therapies in managing type 2 diabetes, obesity, and have demonstrated clinical potential as a treatment for NASH. Ecnoglutide (XW003) is a novel, cAMP signaling biased, long-acting GLP-1 analogue optimized for improved biological activity, cost-effective manufacturing, and once weekly dosing. Currently, the drug is in Phase III stage of its clinical trial for the treatment of Obesity.

  • CT-868: Carmot Therapeutics

CT-868 is a dual GLP-1 and GIP receptor modulator with a unique pharmacological profile optimized for improved tolerability at the GLP-1 receptor. The combined action of GLP-1 and GIP results in greater body weight loss and glucose control. CT-868 is dosed once daily to maximize efficacy and tolerability. CT-868 dual agonist candidate was discovered using the chemotype evolution technology as a peptide-small molecule hybrid compound, able to mimic the native GLP-1 hormone. In the Phase I trial, CT-868 demonstrated compelling pharmacodynamic activity across several clinical measures in overweight and obese healthy individuals a safe and generally well-tolerated profile. Carmot Therapeutics is now expanding the observations in overweight and obese patients with type 2 diabetes to demonstrate CT-868’s effects on glycemic control, weight loss, and tolerability. Currently, the drug is in the Phase II stage of development to treat obesity.

  • DD01: D&D Pharmatech

DD01 is a proprietary, imbalanced dual agonist of GLP-1 and glucagon receptors with a half-life of 11 days in non-human primates. DD01 is being developed as a potential disease-modifying agent for obesity and liver fatty disease. Treatment with DD01 caused weight loss, reduced liver fat, and improved glucose tolerance in preclinical obesity, diabetes, and fatty liver models. In preclinical models of diabetes and nonalcoholic fatty liver disease (NAFLD), DD01 could reduce weight and blood sugar and improve insulin sensitivity and lipid and fat metabolism, which could ameliorate NASH. DD01 demonstrated greater efficacy in preclinical models than semaglutide, an approved GLP-1R receptor agonist; from a mechanical perspective, the effect of DD01 persisted after cessation of treatment. It is currently being evaluated in Phase I clinical trial to investigate the safety, tolerability, PK, and PD of DD01 administered by subcutaneous (SC) injection in overweight/obese subjects with type 2 diabetes mellitus and nonalcoholic fatty liver disease (NAFLD).

The Obesity pipeline report provides insights into

  • The report provides detailed insights about companies that are developing therapies for the treatment of Obesity with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Obesity Treatment.
  • Obesity Companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Obesity Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type.
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Obesity market.

Get a detailed analysis of the latest innovations in the Obesity pipeline. Explore DelveInsight’s expert-driven report today! @ Obesity Unmet Needs

Obesity Companies

Zealand Pharma, Sciwind Biosciences, Genexine, Sirnaomics, Sparrow Pharmaceuticals, Shionogi, Regor Pharmaceuticals, Innovent Biologics, Pfizer, NodThera Limited, Boehringer Ingelheim, Fractyl Health, TransThera, Clearmind Medicine, PegBio, Biolingus, and others.

Obesity pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Obesity Products have been categorized under various ROAs such as

  • Oral
  • Parenteral
  • Intravenous
  • Subcutaneous
  • Topical

Obesity Products have been categorized under various Molecule types such as

  • Recombinant fusion proteins
  • Small molecule
  • Monoclonal antibody
  • Peptide
  • Polymer
  • Gene therapy

Download DelveInsight’s latest report to gain strategic insights into upcoming Obesity Therapies and key Obesity Developments @ Obesity Market Drivers and Barriers, and Future Perspectives

Scope of the Obesity Pipeline Report

  • Coverage- Global
  • Obesity Companies- Zealand Pharma, Sciwind Biosciences, Genexine, Sirnaomics, Sparrow Pharmaceuticals, Shionogi, Regor Pharmaceuticals, Innovent Biologics, Pfizer, NodThera Limited, Boehringer Ingelheim, Fractyl Health, TransThera, Clearmind Medicine, PegBio, Biolingus, and others.
  • Obesity Therapies- APHD-012, Bimagrumab, Semaglutide, CT-868, GLY-200, Bremelanotide, and others.
  • Obesity Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
  • Obesity Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III

Which companies are leading the race in Obesity drug development? Find out in DelveInsight’s exclusive Obesity Pipeline Report—access it now! @ Obesity Emerging Drugs and Major Companies

Table of Contents

  1. Introduction
  2. Executive Summary
  3. Obesity Overview
  4. Obesity Pipeline Therapeutics
  5. Obesity Therapeutic Assessment
  6. Late Stage Products (Phase III)
  7. Survodutide: Zealand Pharma
  8. Drug profiles in the detailed report…..
  9. Mid Stage Products (Phase II)
  10. CT-868: Carmot Therapeutics
  11. Drug profiles in the detailed report…..
  12. Early Stage Products (Phase I)
  13. DD01: D&D Pharmatech
  14. Drug profiles in the detailed report…..
  15. Preclinical and Discovery Stage Products
  16. Drug name: Company name
  17. Drug profiles in the detailed report…..
  18. Inactive Obesity Products
  19. Obesity Key Companies
  20. Obesity Key Products
  21. Obesity Unmet Needs
  22. Obesity Market Drivers
  23. Obesity Market Barriers
  24. Obesity Future Perspectives and Conclusion
  25. Obesity Analyst Views
  26. Obesity Key Companies
  27. Appendix

About Us

DelveInsight is a leading healthcare-focused market research and consulting firm that provides clients with high-quality market intelligence and analysis to support informed business decisions. With a team of experienced industry experts and a deep understanding of the life sciences and healthcare sectors, we offer customized research solutions and insights to clients across the globe. Connect with us to get high-quality, accurate, and real-time intelligence to stay ahead of the growth curve.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Yash Bhardwaj
Email:Send Email
Phone: 09650213330
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/report-store/obesity-pipeline-insight

EPC Consulting Market 2025 : Industry Size to Reach USD 25.67 Billion by 2032, At a CAGR of 8.8%

EPC Consulting Market 2025 : Industry Size to Reach USD 25.67 Billion by 2032, At a CAGR of 8.8%
EPC Consulting Market

Industry Overview

The EPC Consulting Market is experiencing accelerated business growth driven by large-scale infrastructure, energy transition, and digital transformation initiatives. Our proprietary market research reveals an expanding industry size underpinned by sustainability mandates and smart engineering solutions across regions. This EPC consulting market analysis underscores rising demand for integrated project delivery and technical advisory services from 2025 onward.

Market Size and Overview-

The Global EPC Consulting Market size is estimated to be valued at USD 14.22 Bn in 2025 and is expected to reach USD 25.67 Bn by 2032, exhibiting a compound annual growth rate (CAGR) of 8.8% from 2025 to 2032. This market forecast is backed by robust capital expenditure in energy, infrastructure, and petrochemical sectors, reflecting sustained market growth and favorable industry trends.

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Key Takeaways:

Region

• North America: Infrastructure modernization and shale gas EPC projects are boosting regional industry size.

• Latin America: Mining and oilfield development in Brazil and Mexico underpin growing EPC consulting demand.

• Europe: Green energy targets in Germany and France create fresh market opportunities for carbon-neutral EPC.

• Asia Pacific: Rapid urbanization in China and India drives multi-billion-dollar smart city and rail EPC pipelines.

• Middle East: Mega-city developments and petrochemical expansions in UAE and Saudi Arabia dominate market dynamics.

• Africa: Power generation and water management projects in South Africa and Egypt highlight untapped market scope.

Segment Covers

• Service Type:

 – FEED (Front-End Engineering Design): Used in pre-FEED oil & gas projects to reduce costs by 10%.

 – Detailed Engineering: Supports turnkey chemical plants, as seen in a $1.2 Bn Saudi project.

 – Project Management: Employed by utilities for grid modernization in Europe.

• Application:

 – Energy & Power: Solar PV and wind farm EPC consulting captured 18% of total market revenue in 2024.

 – Infrastructure: High-speed rail and metro systems drove 22% year-on-year market growth in Asia Pacific.

 – Petrochemicals: Integrated consulting for ethylene crackers accounted for $2 Bn of global consulting fees.

• End-User:

 – Oil & Gas: Combined upstream and downstream EPC consulting grew by 9% in 2025.

 – Utilities: Smart grid advisory contracts increased 30% in North America.

 – Construction & Real Estate: Urban development projects leveraged BIM-enabled consulting for efficiency gains.

Growth Factors

• Digital Engineering Adoption: In 2024, 35% of global EPC consulting revenue stemmed from digital twins, driving an 8.8% CAGR.

• Sustainability Regulations: Europe’s net-zero roadmaps catalyzed green EPC consulting engagements, up 12% in the past year.

• Cross-Border Mega-Projects: Middle East awarded over $150 Billion in EPC contracts in 2024, elevating global market share for consultancies.

• Infrastructure Stimulus Packages: Asia Pacific stimulus funding exceeded $200 Bn in 2025, fueling demand for integrated EPC advisory services.

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Market Trends

• AI-Driven Optimization: By early 2025, AI in project scheduling cut delivery timelines by 15%, per several recent case studies.

• Modular Construction Integration: 40% of North American EPC consulting assignments in 2024 included prefabrication strategies.

• Digital Twin & IoT Collaboration: Real-time asset performance monitoring grew by 30% in oil & gas consulting orders.

• Cloud-Native Platforms: EPC Consulting Market trends indicate a shift toward SaaS-based engineering tools for real-time collaboration.

Actionable Insights

• Production Capacity: Leading firms expanded digital engineering headcount by 20% in 2024 to meet surging project pipelines.

• Pricing Dynamics: Average EPC consulting fees rose to $120/man-hour in Q1 2025, an 8% premium over 2024 rates.

• Export Flows: Asia Pacific consultancies exported $5 Bn in service contracts to Middle East markets in 2024.

• Use Cases: Predictive maintenance engagements in utilities soared by 25%, unlocking new EPC Consulting Market revenue streams.

• Micro-Indicators: Risk modeling projects expanded by 18% across megaprojects, improving budget forecasts by 10%.

• Nano-Size Indicators: IoT-enabled asset monitoring proofs-of-concept increased by 22% among key players in 2024, indicating rising market share.

Key Players

Wood plc

WorleyParsons

Fluor Corporation

Aecom

Jacobs

SNC-Lavalin

Hatch Ltd

Bechtel Corporation

KBR Inc

TechnipFMC

Chicago Bridge & Iron Company

Hyundai Engineering & Construction

McDermott International Inc

National Projects Construction Corporation

Galfar

Tecnicas Reunidas

Saipem

Daewoo E&C

Petrofac Ltd

Samsung Engineering

Competitive Strategies

• Jacobs’ acquisition of CH2M in 2024 elevated its integrated EPC consulting capabilities, increasing North American market share by 5%.

• Fluor Corporation partnered with leading digital twin providers in 2025 to reduce project cost overruns by 12%.

• WorleyParsons launched a cloud-based FEED platform in 2024, capturing new market opportunities across Asia Pacific and improving operational efficiency by 15%.

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FAQs

1. Who are the dominant players in the EPC Consulting Market?

Major market players include Wood plc, WorleyParsons, Fluor Corporation, Aecom, Jacobs, SNC-Lavalin, Bechtel Corporation, KBR Inc, and TechnipFMC.

2. What will be the size of the EPC Consulting Market in the coming years?

The market size is projected to grow from USD 14.22 Bn in 2025 to USD 25.67 Bn by 2032 at a CAGR of 8.8%.

3. Which end-user industry has the largest growth opportunity?

Energy & Power, particularly renewable energy projects, represent the largest market opportunity, accounting for nearly 20% of total EPC consulting market revenue in 2024.

4. How will market development trends evolve over the next five years?

Key trends include AI-driven optimization, modular construction integration, digital twin & IoT collaboration, and cloud-native engineering platforms reshaping project delivery.

5. What is the nature of the competitive landscape and challenges in the EPC Consulting Market?

Fierce competition among global engineering houses, price pressure from new entrants, and stringent environmental regulations pose ongoing market challenges. Strategic digital partnerships and M&A are common defensive tactics.

6. What go-to-market strategies are commonly adopted in the EPC Consulting Market?

Firms leverage digital transformation alliances, bundled service offerings, strategic acquisitions, and regional partnerships to enhance service scope, capture new projects, and drive business growth.

About Us:

Coherent Market Insights leads into data and analytics, audience measurement, consumer behaviors, and market trend analysis. From shorter dispatch to in-depth insights, CMI has exceled in offering research, analytics, and consumer-focused shifts for nearly a decade. With cutting-edge syndicated tools and custom-made research services, we empower businesses to move in the direction of growth. We are multifunctional in our work scope and have 450+ seasoned consultants, analysts, and researchers across 26+ industries spread out in 32+ countries.

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Credit Risk Assessment Market Global Rising Demand & Huge Scope Till 2032 | Coherent Market Insights

Credit Risk Assessment Market Global Rising Demand & Huge Scope Till 2032 | Coherent Market Insights
Credit Risk Assessment Market

Market Size and Overview

Market Size and Overview- The Global Credit Risk Assessment Market size is estimated to be valued at USD 9.52 Bn in 2025 (market size) and is expected to reach USD 23.97 Bn by 2032 (market forecast), exhibiting a compound annual growth rate (CAGR) of 14.1% from 2025 to 2032. This forecast underscores strong adoption across banking, insurance and corporate finance sectors, supported by evolving market dynamics and rising demand for predictive credit scoring.

Industry Overview

The credit evaluation domain is witnessing accelerated digitization as financial institutions and fintechs deploy advanced analytics and AI-driven models for real-time decision-making. Robust risk governance frameworks and regulatory mandates are driving demand for end-to-end credit risk assessment platforms. Our proprietary market research and market insights reveal a dynamic landscape where legacy systems are being replaced by cloud-native architectures, setting the stage for significant business growth.

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Key Takeaways

Region

• North America: Early adopters of AI-powered scoring engines, driven by stringent regulatory environments.

• Latin America: Growth fueled by microfinance expansions in Brazil and Mexico.

• Europe: GDPR-compliant risk solutions prompting upgrades in Western Europe.

• Asia Pacific: Rapid digitization in India and Southeast Asia accelerating demand.

• Middle East: Infrastructure financing units in UAE and Saudi Arabia integrating advanced analytics.

• Africa: Emerging markets leveraging mobile-driven credit models for unbanked populations.

Segment Covers

• Component:

– Solutions (Credit Scoring, Portfolio Management, Fraud Detection): Example use case—real-time score recalibration in major lenders.

– Services (Consulting, Integration, Support): Example use case—end-to-end deployment with 24/7 support for regional banks.

• Deployment:

– Cloud: Scalable scoring platforms launched by global fintechs.

– On-Premise: Mission-critical systems preferred by tier-1 banks for data sovereignty.

• End-User Industry:

– Banking & Finance: 45% of deals in 2024 for retail and corporate credit risk.

– Telecom & Retail: Use cases include postpaid billing risk and supplier credit profiling.

Growth Factors

• Rising Non-Performing Loans (NPLs): NPL ratios climbed to 4.8% in global banking portfolios in 2024, spurring demand for automated risk monitoring (market drivers).

• AI/ML Integration: Adoption of machine learning algorithms grew 28% year-on-year in 2024, enhancing predictive accuracy (industry size).

• Regulatory Pressure: Basel III and IFRS 9 compliance programs accounted for 35% of new license revenues (Credit Risk Assessment Market revenue).

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Market Trends

• Real-Time Risk Monitoring: Over 60% of new deployments in 2025 offer continuous score updates (Credit Risk Assessment Market share).

• Open Banking APIs: Data sharing initiatives led to a 22% rise in third-party risk data utilization (market trends).

• Explainable AI: Transparency requirements driving investment in model interpretability frameworks, with 18% more R&D projects in 2024 (industry trends).

Actionable Insights

Supply-Side Indicators

• New Solution Releases: Grew from 150 in 2024 to 210 in 2025, boosting overall production capacity by 40%.

• Average License Pricing: Increased by 8% in 2024 as vendors bundled AI modules (market scope).

• Export Penetration: APAC exports accounted for 30% of total software shipments in 2024.

Demand-Side Indicators

• Imports: Financial institutions in Latin America imported 45% of their risk platforms in 2024.

• Use Cases Across Industries: BFSI accounted for 50% of new subscriptions, telecom 15%, retail 10%.

• Nano-Indicators: Average daily risk checks per client rose from 2.1 million to 3.4 million in 2024 (market dynamics).

Key Players

• Experian

• Equifax

• TransUnion

• FICO

• Moody’s Analytics

• Oracle

• IBM

• SAP

• SAS Institute

• Fiserv

• Pegasystems

• Genpact

• ACL

• Kroll

• PRMIA

• Riskonnect

• RiskSpotter

• Riskdata

• BRASS

• Misys

Competitive Strategies

• Experian’s 2024 acquisition of an AI-analytics startup drove a 15% uptick in Credit Risk Assessment Market report revenues.

• FICO launched a cloud-native scoring service in Q3 2024, boosting its market share by 5% in North America.

• Oracle partnered with leading regional banks in Asia Pacific for embedded risk modules, resulting in a 20% increase in subscription renewals.

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FAQs

1. Who are the dominant players in the Credit Risk Assessment Market?

Dominant players include Experian, Equifax, FICO, Moody’s Analytics and Oracle, each leading with unique AI-driven scoring and compliance solutions.

2. What will be the size of the Credit Risk Assessment Market in the coming years?

The Credit Risk Assessment Market size is projected to grow from USD 9.52 Bn in 2025 to USD 23.97 Bn by 2032 at a CAGR of 14.1%.

3. Which end-user industry has the largest growth opportunity?

Banking & Finance leads with over 45% of new deployments in 2024, but telecom and retail segments are expanding at 12–15% annually.

4. How will market development trends evolve over the next five years?

Expect real-time risk monitoring, explainable AI, and open banking integrations to dominate, driving faster implementation cycles and modular pricing models.

5. What is the nature of the competitive landscape and challenges in the Credit Risk Assessment Market?

Competition centers on AI accuracy, regulatory compliance and cloud versus on-premise offerings; challenges include data privacy and model interpretability.

6. What go-to-market strategies are commonly adopted in the Credit Risk Assessment Market?

Partnerships with regional banks, cloud bundling with ERP suites, acquisition of analytics startups, and outcome-based pricing models are widely used growth strategies.

About Us:

Coherent Market Insights leads into data and analytics, audience measurement, consumer behaviors, and market trend analysis. From shorter dispatch to in-depth insights, CMI has exceled in offering research, analytics, and consumer-focused shifts for nearly a decade. With cutting-edge syndicated tools and custom-made research services, we empower businesses to move in the direction of growth. We are multifunctional in our work scope and have 450+ seasoned consultants, analysts, and researchers across 26+ industries spread out in 32+ countries.

Media Contact
Company Name: Coherent Market Insights
Contact Person: Mr Shah
Email:Send Email
Phone: 12524771362
Address:Coherent Market Insights Pvt Ltd, 533 Airport Boulevard,
City: Burlingame
State: Burlingame
Country: India
Website: https://www.coherentmarketinsights.com/industry-reports/credit-risk-assessment-market

Oncology Information System Market to Reach USD 4.80 Billion by 2030 at a CAGR of 8.5%, Driven by Growing Digital Health Adoption and Rising Cancer Burden

Oncology Information System Market to Reach USD 4.80 Billion by 2030 at a CAGR of 8.5%, Driven by Growing Digital Health Adoption and Rising Cancer Burden
Oncology Information System Market
Mordor Intelligence has published a new report on the Oncology Information System Market, offering a comprehensive analysis of trends, growth drivers, and future projections.

Introduction

Mordor Intelligence, in its latest oncology information system market report, forecasts that the global oncology information system market will grow significantly, reaching an estimated USD 4.80 billion by 2030 from USD 3.20 billion by 2025. The oncology information system (OIS) market is gaining importance as healthcare providers seek more efficient, accurate, and integrated methods to manage cancer care. These systems are designed to capture, store, and manage patient-specific cancer treatment information, covering aspects such as diagnosis, planning, scheduling, treatment, and follow-up. OIS solutions play a critical role in improving clinical workflows, reducing medical errors, and supporting multidisciplinary teams involved in cancer care.

Key Trends

The oncology information system (OIS) market is experiencing steady expansion thanks to several notable trends:

1. Rising Cancer Incidence and Cancer Care Needs Global cancer cases surged to around 18 million new diagnoses in 2020, escalating the urgency for systems capable of comprehensive patient data management throughout the care continuum.

2. Government Initiatives and Funding Support Increased investment by governments and research institutions, such as the USD 7.3 billion allocation to the National Cancer Institute (including USD 216 million for Cancer Moonshot), supports enhanced patient data capture and improved cancer care infrastructure.

3. Digital Health Technologies Driving OIS Adoption Healthcare facilities are integrating advanced OIS software such as patient information systems and treatment planning tools with AI and ML capabilities to streamline workflows, cut errors, and foster data driven decision making.

4.Post‑Pandemic Recovery Projecting Renewed Growth While OIS implementation slowed during the COVID‑19 surge, the market has bounced back, with delayed implementations resuming and contributing to renewed growth momentum.

5. Regional Adoption Led by North America North America held over 42% market share in 2022 driven by robust healthcare IT systems and favorable policies with significant investments from Asia-Pacific and other regions further boosting adoption.

 

Market Segmentation

The oncology information system market breakdown spans products, applications, and end users:

By Oncology

The market is categorized into two primary offerings:

  • Software: Constituting approximately 83% of the market in 2022. This includes:

Patient Information Systems: Crucial for medical history, treatment documentation, and care coordination.

Treatment Planning Systems: Tailored radiation and medical oncology planning.

 

  • Services: Providing implementation support, training, and ongoing maintenance

 

By Application

Systems are deployed across different oncology domains

Medical Oncology: Medical Oncology focuses on the treatment of cancer using systemic therapies such as chemotherapy, immunotherapy, hormone therapy, and targeted therapy. Medical oncologists manage patient care before, during, and after treatment, often in collaboration with other oncology specialists. In an OIS, medical oncology modules help in documenting drug regimens, scheduling cycles, tracking side effects, and maintaining treatment histories to ensure continuity and safety in care.

Surgical Oncology: Surgical oncology involves the diagnosis, staging, and removal of tumors through surgical intervention. It plays a critical role in cancer treatment, especially when physical removal of the tumor is essential. Within an oncology information system, surgical oncology workflows include surgical planning, integration with imaging and pathology reports, and post-operative monitoring. These tools support better clinical decision-making and enhance coordination among care teams.

Radiation Oncology: Radiation oncology uses high-energy radiation to destroy cancer cells or shrink tumors. It includes external beam radiation therapy and brachytherapy, among others. OIS platforms designed for radiation oncology often integrate treatment planning systems, simulate sessions, track dosage administration, and manage imaging data. This ensures accuracy in treatment delivery and supports compliance with safety protocols and quality assurance standards.

By End User

The primary consumers of OIS are:

Hospitals: Hospitals are the largest users of oncology information systems, often managing high volumes of cancer patients across various departments. These facilities require robust, integrated OIS platforms to coordinate care among radiation oncology, medical oncology, surgical teams, and diagnostic units. OIS helps hospitals streamline workflows, centralize patient records, monitor treatment outcomes, and comply with regulatory standards, all while supporting multidisciplinary cancer care.

Oncology Clinics: Oncology clinics specialize in the diagnosis and treatment of cancer and often provide outpatient services. These clinics rely on OIS solutions to manage scheduling, chemotherapy administration, follow-ups, and patient education. Given their focused approach to cancer care, clinics benefit from systems that offer tailored oncology modules, improve operational efficiency, and enhance communication between specialists and patients.

Research & Academic Centers: Research and academic institutions use oncology information systems primarily for clinical research, data analysis, and medical education. These centers benefit from advanced data capture features, integration with clinical trial systems, and tools for outcome tracking and reporting. OIS platforms in these settings support evidence-based practices, facilitate longitudinal studies, and help train the next generation of oncology professionals.

 

By Geography

Europe: Europe holds a significant portion of the market, propelled by investments in healthcare modernization, cancer care initiatives, and requirements for interoperability. Countries such as Germany, France, Italy, Spain, and the UK are at the forefront of adopting oncology information systems to streamline patient data management, integrate radiotherapy planning, and support value-based care frameworks.

Asia-Pacific: The Asia-Pacific region is the fastest growing segment in the OIS market, with an estimated CAGR of 9.85% between 2025 and 2030. Expansion reflects a surge in healthcare infrastructure development, increased digital transformation efforts, and growing cancer incidence. Markets such as China, Japan, India, South Korea, and Australia are accelerating adoption via cloud-based OIS deployments and national cancer care strategies.

Middle East & Africa: Middle East and Africa, including the Gulf Cooperation Council (GCC) countries and South Africa, are seeing gradual yet steady growth. Healthcare systems are increasingly investing in oncology IT as part of broader cancer control and digital health initiatives. While adoption lags behind North America and Europe, the region is expected to gain traction as government and private-sector support expands.

South America: South America’s OIS market is progressing steadily, driven by growing cancer care infrastructure and digitization efforts in healthcare institutions across Brazil, Argentina, and neighboring countries. As hospitals and specialty clinics invest in digital platforms, oncology information systems are becoming instrumental in standardizing patient records, treatment planning, and data reporting.

 

Key Players

The OIS market features several established and emerging companies:

  • Oracle: Delivers integrated oncology modules as part of its comprehensive healthcare IT suite.

  • Siemens Healthineers: Offers robust radiotherapy planning solutions and clinical data systems.

  • Elekta: Specializes in radiation oncology software, including precision treatment planning.

  • Koninklijke Philips N.V: recognized as a leading provider in the oncology information system market. The company offers a range of software modules and clinical workflows that integrate cancer care management.

  • McKesson Corporation: Mckesson Corporation also ranks among the major players in the global oncology information system sector. The company's platforms are built to manage chemotherapy workflows, medication tracking, and clinical data exchange

 

Conclusion

The global oncology information system market is poised for strong growth, projecting from USD 3.20 billion in 2025 to USD 4.80 billion by 2030, riding an annual growth rate of around 8.5%.

This expansion is driven by several converging forces: rising cancer cases, supportive policy frameworks, digital innovation in healthcare, and enhanced implementation pace post COVID. North America leads adoption, but Asia-Pacific and other regions are closing thanks to infrastructure improvements and heightened digital health investments.

Looking ahead, as software platforms integrate AI, machine learning, and data analytics, and as service models evolve to meet diverse institutional needs, OIS will become even more central to oncology care delivery, enabling better workflow coordination, patient outcomes, and cost efficiencies. The competitive landscape is vibrant, with both established players and new entrants contributing to ecosystem development through strategic mergers and partnerships.

In summary, the oncology information system market is entering a mature growth phase. Its capacity to respond to pressing clinical and administrative demands, combined with sustained R&D and funding initiatives, ensures that healthcare providers worldwide will continue to invest in these platforms transforming cancer care across the globe.

 

Industry Related Reports

Oncology Based In-Vivo CRO Market: The Global Oncology-Based In-Vivo Contract Research Organization (CRO) Market report is segmented by Indication (Blood Cancer, Solid Tumors, and Other Indications), Model (Syngeneic, Xenograft, and Patient-Derived Xenograft (PDX)), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, and South America). The report provides the market value (in USD million) for all the above segments.

 

Oncology Clinical Trials Market: The Oncology Clinical Trials Market report is segmented by Phase (Phase I, Phase II, Phase III, Phase IV), Design (Treatment Studies and Observational Studies), Cancer Type (Lung Cancer, Breast Cancer, and Others), Therapeutic Modality (Immunotherapy and Others), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, and South America). The report provides market forecasts in terms of value (USD).

 

For More Insights: https://www.mordorintelligence.com/industry-reports/oncology-clinical-trials-market?utm_source=abnewswire

 

Precision Oncology Market: The Precision Oncology Market report is segmented by Type (Therapeutics and Diagnostics), Cancer Type (Breast Cancer, Lung Cancer, Colorectal Cancer, Prostate Cancer, and Other Cancer Types), End-User (Hospitals, Diagnostic Laboratories, Pharmaceutical & Biotechnology Companies, and Research & Academic Institutes), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, and South America).

 

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