DelveInsight’s "Congenital Adrenal Hyperplasia Pipeline Insight 2025" report provides comprehensive insights about 5+ companies and 8+ pipeline drugs in the Congenital Adrenal Hyperplasia pipeline landscape. It covers the Congenital Adrenal Hyperplasia pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Congenital Adrenal Hyperplasia pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
Curious about the latest updates in the Congenital Adrenal Hyperplasia Pipeline? Click here to explore the therapies and trials making headlines @ Congenital Adrenal Hyperplasia Pipeline Outlook Report
Key Takeaways from the Congenital Adrenal Hyperplasia Pipeline Report
- On 23 September 2025, Crinetics Pharmaceuticals Inc. announced a Phase 2 sequential dose cohort study will evaluate the efficacy, safety, PK, and PD of atumelnant (CRN04894) when administered for 12 weeks in participants with CAH caused by 21-hydroxylase deficiency. Up to 42 participants will be enrolled in the study.
- On 10 September 2025, H. Lundbeck A/S conducted a clinical trial will evaluate the effects of different doses of Lu AG13909 in adult participants with congenital adrenal hyperplasia, also called CAH. CAH is a rare genetic disorder that affects a person's ability to produce certain hormones. The main goals of this trial are to learn about the safety and tolerability of Lu AG13909, how Lu AG13909 behaves in the body, and how the body responds to Lu AG13909.
- DelveInsight’s Congenital Adrenal Hyperplasia Pipeline report depicts a robust space with 5+ active players working to develop 8+ pipeline therapies for Congenital Adrenal Hyperplasia treatment.
- The leading Congenital Adrenal Hyperplasia Companies such as Neurocrine Biosciences, Inc, Spruce Biosciences, Lundbeck, and others.
- Promising Congenital Adrenal Hyperplasia Therapies such as Atumelnant (CRN04894), SPR001, Lu AG13909, Crinecerfont, ATR-101, Chronocort, Hydrocortisone, NBI-74788, SPR001, Osilodrostat, LIK066 and others.
Want to know which companies are leading innovation in Congenital Adrenal Hyperplasia? Dive into the full pipeline insights @ Congenital Adrenal Hyperplasia Clinical Trials Assessment
The Congenital Adrenal Hyperplasia Pipeline Report provides disease overview, pipeline scenario and therapeutic assessment of the key pipeline therapies in this domain. The Congenital Adrenal Hyperplasia Pipeline Report also highlights the unmet needs with respect to the Congenital Adrenal Hyperplasia.
Congenital Adrenal Hyperplasia Overview
Congenital Adrenal Hyperplasia (CAH) is a group of genetic disorders affecting the adrenal glands, leading to impaired production of cortisol and aldosterone. The most common form, 21-hydroxylase deficiency, results in excess androgen production, causing ambiguous genitalia in females and early puberty in both genders. CAH can cause severe dehydration and salt loss in the classic form, requiring lifelong management with hormone replacement therapy. Early diagnosis and treatment are crucial for preventing serious complications and improving quality of life.
Congenital Adrenal Hyperplasia Emerging Drugs Profile
- Atumelnant - Crinetics Pharmaceuticals
Atumelnant is investigational compound, is the first once-daily, oral adrenocorticotropic hormone (ACTH) receptor antagonist that acts selectively at the melanocortin type 2 receptor (MC2R) on the adrenal gland. Diseases associated with excess ACTH can have significant impact on physical and mental health. Atumelnant has exhibited strong binding affinity for MC2R in preclinical models and has demonstrated suppression of adrenally derived glucocorticoids and androgens that are under the control of ACTH. Data from a 12-week Phase 2 study demonstrated compelling treatment benefits of atumelnant, evidenced by the rapid, substantial and sustained statistically significant reductions in key CAH disease related biomarkers, including androstenedione and 17-hydroxyprogesterone, in a diverse population. Atumelnant is currently in development for congenital adrenal hyperplasia and ACTH-dependent Cushing’s syndrome. Currently the drug is in Phase II stage of its development for the treatment of Congenital adrenal hyperplasia.
If you’re tracking ongoing Congenital Adrenal Hyperplasia Clinical trials, this press release is a must-read. Tap to see the breakthroughs @ Congenital Adrenal Hyperplasia Treatment Drugs
The Congenital Adrenal Hyperplasia Pipeline report provides insights into:-
- The report provides detailed insights about companies that are developing therapies for the treatment of Congenital Adrenal Hyperplasia 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 Congenital Adrenal Hyperplasia Treatment.
- Congenital Adrenal Hyperplasia Companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
- Congenital Adrenal Hyperplasia 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 Congenital Adrenal Hyperplasia market.
Congenital Adrenal Hyperplasia Companies
Neurocrine Biosciences, Inc, Spruce Biosciences, Lundbeck, and others
Congenital Adrenal Hyperplasia pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
- Intravenous
- Subcutaneous
- Oral
- Intramuscular
Congenital Adrenal Hyperplasia Products have been categorized under various Molecule types such as
- Monoclonal antibody
- Small molecule
- Peptide
From emerging drug candidates to competitive intelligence, the Congenital Adrenal Hyperplasia Pipeline Report covers it all – check it out now @ Congenital Adrenal Hyperplasia Market Drivers and Barriers, and Future Perspectives
Scope of the Congenital Adrenal Hyperplasia Pipeline Report
- Coverage- Global
- Congenital Adrenal Hyperplasia Companies- Neurocrine Biosciences, Inc, Spruce Biosciences, Lundbeck, and others
- Promising Congenital Adrenal Hyperplasia Therapies- Atumelnant (CRN04894), SPR001, Lu AG13909, Crinecerfont, ATR-101, Chronocort, Hydrocortisone, NBI-74788, SPR001, Osilodrostat, LIK066 and others.
- Congenital Adrenal Hyperplasia Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
- Congenital Adrenal Hyperplasia Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
Stay ahead in Healthcare Research – discover what’s next for the Congenital Adrenal Hyperplasia Treatment landscape in this detailed analysis @ Congenital Adrenal Hyperplasia Emerging Drugs and Major Players
Table of Contents
- Introduction
- Executive Summary
- Congenital Adrenal Hyperplasia: Overview
- Pipeline Therapeutics
- Therapeutic Assessment
- Congenital Adrenal Hyperplasia– DelveInsight’s Analytical Perspective
- Late Stage Products (Phase III)
- Drug Name: Company Name
- Drug profiles in the detailed report…..
- Mid Stage Products (Phase II)
- Atumelnant: Crinetics Pharmaceuticals
- Drug profiles in the detailed report…..
- Early Stage Products (Phase I/II)
- Drug Name: Company Name
- Drug profiles in the detailed report…..
- Preclinical and Discovery Stage Products
- Drug Name: Company Name
- Drug profiles in the detailed report…..
- Inactive Products
- Congenital Adrenal Hyperplasia Key Companies
- Congenital Adrenal Hyperplasia Key Products
- Congenital Adrenal Hyperplasia- Unmet Needs
- Congenital Adrenal Hyperplasia- Market Drivers and Barriers
- Congenital Adrenal Hyperplasia- Future Perspectives and Conclusion
- Congenital Adrenal Hyperplasia Analyst Views
- Congenital Adrenal Hyperplasia Key Companies
- Appendix
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