TheraRadar

Duodenal Ulcer

Gastrointestinal 0 original drugs
0
Novel Drugs
7
Reformulations
0
Active Trials
6
Drug Targets

Gastrointestinal indication. Duodenal Ulcer has 0 FDA-approved novel treatments across 6 drug targets. Explore market leaders, treatments by mechanism, the clinical pipeline, and drug targets below.

Phase 3 Readouts Pro

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

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Q3 2026
Ilaprazole
Il-Yang Pharm. Co., Ltd.
Estimated · stale NCT06284876
Q3 2027
JP-1366 10 mg
Onconic Therapeutics Inc.
Estimated · stale NCT06439563

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.

Duodenal Ulcer Treatments by Mechanism

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

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H+/K+ ATPase
1 trials 1 sponsor
5-HT1B/5-HT1D/COX-1/COX-2
1 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.

Duodenal Ulcer Clinical Pipeline by Phase

50 industry-sponsored trials across 21 sponsors

Precision Medicine Biomarkers

All biomarkers →

Biomarkers used for patient selection in Duodenal Ulcer

Novel Duodenal Ulcer Drugs by Company (New molecular entities)

No novel drugs found for this indication.

Reformulations (7 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.

Duodenal Ulcer Drug Targets

Molecular targets of approved and investigational Duodenal Ulcer drugs — 6 targets tracked.

Generic Drugs (8 ANDA approved) Click to expand

Related Indications

Other Gastrointestinal indications

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