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Cervical Cancer

Oncology 3 original drugs
3
Novel Drugs
6
Reformulations
262
Active Trials
4
Drug Targets

Phase 3 Readouts Pro

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

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Q2 2026
AK104
Akeso
Estimated · stale NCT05235516
Q3 2026
Recombinant humanized anti-PD-1 monoclonal antibody injection
Bio-Thera Solutions
Estimated · stale NCT06123884
Q3 2027
Socazolimab+cisplatin/carboplatin+paclitaxel+Bevacizumab
Lee's Pharmaceutical Limited
Estimated · aging NCT06459687
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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 6 mechanisms across 8 industry trials with a known mechanism of action.

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Programmed Death Receptor-1 Blocking Antibody
3 trials 2 active 1 sponsor
Tissue Factor/Tubulin
1 trials 1 active 1 sponsor
Programmed Death Ligand-1 Blocker
1 trials 1 sponsor
Vascular Endothelial Growth Factor Inhibitor
1 trials 1 sponsor
Nuclear Export Inhibitor
1 trials 1 sponsor
Kinase 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

204 industry-sponsored trials across 136 sponsors

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Precision Medicine Biomarkers

All biomarkers →

Biomarkers used for patient selection in Cervical 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 (2 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