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Ovarian Cancer

Oncology 5 original drugs
5
Novel Drugs
6
Reformulations
540
Active Trials
11
Drug Targets

Phase 3 Readouts Pro

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

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Q2 2026
SHR-A1921
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Estimated · stale NCT06394492
Q2 2026
SHR-1921
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Estimated · stale NCT06211023
Q2 2026
olvimulogene nanivacirepvec
Genelux Corporation
Estimated · fresh NCT05281471
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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.

Treatments by Mechanism

Top 12 mechanisms across 45 industry trials with a known mechanism of action.

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Poly(ADP-Ribose) Polymerase Inhibitor
11 trials 4 active 2 sponsors
Microtubule Inhibitor
8 trials 1 active 6 sponsors
Programmed Death Receptor-1 Blocking Antibody
7 trials 1 active 4 sponsors
Platinum-based Drug
5 trials 1 active 4 sponsors
Vascular Endothelial Growth Factor Inhibitor
4 trials 1 active 3 sponsors
Programmed Death Ligand-1 Blocker
3 trials 1 active 2 sponsors
DNA
2 trials 1 active 2 sponsors
ALK/ROS1/NTRK1/TRKB/TRKC
1 trials 1 active 1 sponsor
AXL/FLT-3/KIT/MER/MET/RET/ROS1/TIE-2/TRKB/TYRO3/VEGFR-1/VEGFR-2/VEGFR-3
1 trials 1 active 1 sponsor
PIK3CA
1 trials 1 sponsor
Alkylating Drug
1 trials 1 sponsor
Nuclear Export Inhibitor
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.

Clinical Pipeline by Phase

636 industry-sponsored trials across 318 sponsors

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Precision Medicine Biomarkers

All biomarkers →

Biomarkers used for patient selection in Ovarian Cancer

Reformulations (6 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.

Generic Drugs (1 ANDA approved) Click to expand

Generic drugs contain the same active ingredient as the brand-name drug and are approved via ANDA (Abbreviated New Drug Application).

Related Indications

Other Oncology 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