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Trials
A Clinical Trial to Evaluate the Safety and Efficacy of COM701 in Relapsed Platinum Sensitive Ovarian Cancer

trialsTrialRecruiting

A Clinical Trial to Evaluate the Safety and Efficacy of COM701 in Relapsed Platinum Sensitive Ovarian Cancer

A phase 1/2 trial of COM701 in ovarian cancer, run by Compugen Ltd, now recruiting.

Overview Connected3

Overview

A Clinical Trial to Evaluate the Safety and Efficacy of COM701 in Relapsed Platinum Sensitive Ovarian Cancer is a phase 1/2 interventional study registered as NCT06888921 by Compugen Ltd, with 60 participants planned, started 2025-07-21 and due to reach its primary completion in 2027-03. Interventions recorded: COM701 and Normal Saline.

Setting

An Adaptive Clinical Platform Trial to Evaluate the Safety and Efficacy of COM701 as Monotherapy or Combination Therapy as Maintenance Therapy in Participants With Relapsed Platinum Sensitive Ovarian Cancer (PSOC)

Phase

Phase 1/2

Sponsor

Compugen Ltd

Registry

Started

2025-07-21

Enrolled

60 enrolled

Connected

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cancers

Ovarian cancer Platinum-sensitive ovarian cancer

companies

Evidence strength17/100 · Preliminary

How much and what kind of evidence, not how big the benefit. Click for the breakdown.

Phase 1/2+8
60 enrolled+9
No structured primary endpoint0
Result: recruiting0
No independent replication recorded0

Formula disclosed on the evidence page.

ProvenanceLast edited 2026-09-18 · Jude Gomila · Link 1,018 registry trials to cancer subtype pages by dri… · diff · file

Sources & links

ClinicalTrials.gov NCT06888921

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Ovarian cancer
Platinum-sensitive ovarian cancer

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