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Congenital Adrenal Hyperplasia

0 original drugs
0
Novel Drugs
9
Reformulations
0
Active Trials
1
Drug Targets

Congenital Adrenal Hyperplasia has 0 FDA-approved novel treatments across 1 drug target. Explore market leaders, treatments by mechanism, the clinical pipeline, and drug targets below.

Phase 3 Readouts Pro

3 active Phase 3 trials with confidence-graded completion dates.

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Q2 2027
Atumelnant
Crinetics Pharmaceuticals Inc.
Estimated · fresh NCT07144163
Q1 2030
Atumelnant
Crinetics Pharmaceuticals Inc.
Estimated · fresh NCT07159841
Q1 2026
Chronocort
Immedica Pharma AB
Completed · awaiting NCT05299554

Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Congenital Adrenal Hyperplasia Treatments by Mechanism

Top 2 mechanisms across 6 industry trials with a known mechanism of action.

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Corticotropin-releasing Factor Type 1 Receptor Antagonist
4 trials 3 active 1 sponsor
Corticosteroid
2 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Congenital Adrenal Hyperplasia Clinical Pipeline by Phase

26 industry-sponsored trials across 9 sponsors

Novel Congenital Adrenal Hyperplasia Drugs by Company (New molecular entities)

No novel drugs found for this indication.

Reformulations (9 drugs) Click to expand

Reformulations are FDA-approved versions of existing molecules in new dosage forms (e.g., oral solution vs tablet, extended-release vs immediate-release). They require a new NDA but use an already-proven active ingredient.

Congenital Adrenal Hyperplasia Drug Targets

Molecular targets of approved and investigational Congenital Adrenal Hyperplasia drugs — 1 target tracked.

Generic Drugs (5 ANDA approved) Click to expand

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology