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Active, not recruiting Phase 2 Interventional Results available

Randomized Trial of Topotecan With M6620, an ATR Kinase Inhibitor, in Small Cell Lung Cancers and Small Cell Cancers Outside of the Lungs

ClinicalTrials.gov ID: NCT03896503

Public ClinicalTrials.gov record NCT03896503. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 3:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized Phase II Trial of Topotecan Plus M6620 (VX-970, Berzosertib) Vs. Topotecan Alone in Patients With Relapsed Small-Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase II trial studies how well berzosertib (M6620) works when given in combination with topotecan hydrochloride (topotecan) compared with topotecan alone in treating patients with small cell lung cancer that has come back (relapsed), or small cell cancer that arises from a site other than the lung (extrapulmonary). Drugs used in chemotherapy, such as topotecan hydrochloride, work by damaging the DNA (deoxyribonucleic acid) in tumor cells, causing those cells to die and the tumor to shrink. However, some tumor cells can become less affected by chemotherapy because they have ways to repair the damaged DNA. The addition of M6620 could help topotecan hydrochloride shrink the cancer and prevent it from returning by blocking enzymes needed for DNA repair.

Study identification

NCT ID
NCT03896503
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
104 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 30, 2019 (Actual)
Primary completion
Dec 19, 2022 (Actual)
Completion
May 13, 2027 (Estimated)
Last update posted
Jul 31, 2026

2019 – 2027

United States locations

U.S. sites
33
U.S. states
12
U.S. cities
29
Facility City State ZIP Site status
Los Angeles General Medical Center Los Angeles California 90033 —
USC / Norris Comprehensive Cancer Center Los Angeles California 90033 —
USC Norris Oncology/Hematology-Newport Beach Newport Beach California 92663 —
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
UCHealth University of Colorado Hospital Aurora Colorado 80045 —
University of Kansas Clinical Research Center Fairway Kansas 66205 —
HaysMed Hays Kansas 67601 —
University of Kansas Cancer Center Kansas City Kansas 66160 —
Lawrence Memorial Hospital Lawrence Kansas 66044 —
The University of Kansas Cancer Center - Olathe Olathe Kansas 66061 —
University of Kansas Cancer Center-Overland Park Overland Park Kansas 66210 —
University of Kansas Hospital-Indian Creek Campus Overland Park Kansas 66211 —
Mercy Hospital Pittsburg Pittsburg Kansas 66762 —
Salina Regional Health Center Salina Kansas 67401 —
University of Kansas Health System Saint Francis Campus Topeka Kansas 66606 —
University of Kansas Hospital-Westwood Cancer Center Westwood Kansas 66205 —
University of Kentucky/Markey Cancer Center Lexington Kentucky 40536 —
NCI - Center for Cancer Research Bethesda Maryland 20892 —
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201 —
Weisberg Cancer Treatment Center Farmington Hills Michigan 48334 —
University Health Truman Medical Center Kansas City Missouri 64108 —
University of Kansas Cancer Center - North Kansas City Missouri 64154 —
University of Kansas Cancer Center - Lee's Summit Lee's Summit Missouri 64064 —
University of Kansas Cancer Center at North Kansas City Hospital North Kansas City Missouri 64116 —
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center Lebanon New Hampshire 03756 —
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York New York 10016 —
Wake Forest University at Clemmons Clemmons North Carolina 27012 —
Wake Forest Baptist Health - Hematology Oncology - Statesville Statesville North Carolina 28677 —
Wake Forest Baptist Health - Wilkes Medical Center Wilkesboro North Carolina 28659 —
Wake Forest University Health Sciences Winston-Salem North Carolina 27157 —
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
Parkland Memorial Hospital Dallas Texas 75235 —
UT Southwestern/Simmons Cancer Center-Dallas Dallas Texas 75390 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03896503, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 31, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03896503 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →