CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 76 enrolled
Drug / intervention
Berzosertib +2 moredrug
Likely dose
Berzosertib 105 milligramsfrom 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/NCT04768296
NCT04768296Phase 2Completed

A Phase II, Open-label, Single-arm Study of Berzosertib (M6620) in Combination With Topotecan in Participants With Relapsed Platinum-resistant Small-Cell Lung Cancer (DDRiver SCLC 250)

EMD Serono Research & Development Institute, Inc.·interventional·Posted Feb 24, 2021·Updated Sep 26, 2024

In Brief

A Phase 2 clinical trial evaluating Berzosertib and Topotecan for Small-cell Lung Cancer. Completed, enrolled 76 participants across 51 sites in 7 countries.

Detailed Summary

The main purpose of this study is to assess efficacy, safety, tolerability and pharmacokinetics (PK) of Berzosertib in combination with Topotecan in participants with relapsed, platinum-resistant small-cell lung cancer (SCLC). This study will be conducted in two parts: safety run-in part and main part. The safety run-in part will be conducted in Japan.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, China, France, Italy, Japan, Spain, United States

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedFeb 24, 2021
Enrollment StartMar 29, 2021
Primary CompletionJul 21, 2023
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 5.4 years ago

Interventions

Berzosertibdrug

Participants received Berzosertib at a dose of 105 milligrams per square meter (mg/m\^2 ) intravenously on Day 2 and Day 5 of each 21-day cycle until disease progression or other criteria for study intervention discontinuation are met.

Berzosertibdrug

Participants received Berzosertib at a dose of 210 mg/m\^2 intravenously on Day 2 and Day 5 of each 21-day cycle in DL2 of safety run-in part and main part until disease progression or other criteria for study intervention discontinuation are met.

Topotecandrug

Participants received Topotecan at a dose of 1.25 mg/m\^2 intravenously on Days 1 through 5 of each 21-day cycle in DL1 and DL2 of safety run-in part and main part until disease progression or other criteria for study intervention discontinuation are met.