CI

At a glance

ClinicalIndex Comparison Record
Phase 1Active· 35 enrolled / 35 target
Drug / intervention
Berzosertib +4 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02627443
NCT02627443Phase 1ActiveUpdate Overdue (0.3/mo)Completion was 20mo ago

Phase 1 Dose Escalation and Expansion Cohort of Carboplatin and Gemcitabine With or Without M6620 (VX-970) in First or Second Recurrence Platinum-Sensitive Epithelial Ovarian, Peritoneal, and Fallopian Tube Cancer

National Cancer Institute (NCI)·interventional·Posted Dec 11, 2015·Updated Jun 29, 2026

In Brief

A Phase 1 clinical trial evaluating Berzosertib, Carboplatin, and 3 other interventions for Metastatic Fallopian Tube Carcinoma and 11 related conditions. Active but no longer recruiting, targeting 35 participants across 14 sites.

Signals

Enrollment appears stalled

Detailed Summary

This phase I trial studies the side effects and best dose of gemcitabine hydrochloride and berzosertib when given together with carboplatin in treating patients with ovarian, primary peritoneal, or fallopian tube cancer that has come back (recurrent) and has spread to other places in the body (metastatic). Chemotherapy drugs, such as carboplatin and gemcitabine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Berzosertib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving berzosertib with chemotherapy (carboplatin and gemcitabine hydrochloride) may work better in treating patients with ovarian, primary peritoneal, or fallopian tube cancer compared to chemotherapy alone.

Study Details

Timeline

Phase 1Active
201620172018201920202021202220232024202520262027
First PostedDec 11, 2015
Enrollment StartMay 16, 2017
Primary CompletionOct 4, 2024
Study CompletionJun 3, 2027
TodayJul 2, 2026
Enrollment to primary: 7.4 yearsPosted 10.6 years ago

Arms & Interventions

Treatment (carboplatin, gemcitabine hydrochloride, VX-970)experimental

Patients receive carboplatin IV over 30 minutes on day 1, gemcitabine hydrochloride IV over 30 minutes on days 1 and 8, and berzosertib IV over 60 minutes on days 2 and 9. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Drug: BerzosertibDrug: CarboplatinDrug: Gemcitabine HydrochlorideOther: Laboratory Biomarker AnalysisOther: Pharmacological Study

Interventions

Berzosertibdrug

Given IV

Carboplatindrug

Given IV

Gemcitabine Hydrochloridedrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Pharmacological Studyother

Correlative studies