Active, not recruitingPHASE1, PHASE2NCT04216316
Testing the Addition of an Anti-cancer Drug, Berzosertib (M6620, VX-970), to the Usual Treatments (Carboplatin and Gemcitabine) and to Pembrolizumab for Patients With Advanced Squamous Cell Non-small Cell Lung Cancer
Studying NON RARE IN EUROPE: Non-small cell lung cancer
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- National Cancer Institute (NCI)
- Principal Investigator
- Liza C VillaruzUniversity of Pittsburgh Cancer Institute LAO
- Intervention
- Berzosertib(drug)
- Enrollment
- 12 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2027
Study locations (30)
- Keck Medicine of USC Koreatown, Los Angeles, California, United States
- Los Angeles General Medical Center, Los Angeles, California, United States
- USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States
- USC Norris Oncology/Hematology-Newport Beach, Newport Beach, California, United States
- UM Sylvester Comprehensive Cancer Center at Aventura, Aventura, Florida, United States
- UM Sylvester Comprehensive Cancer Center at Coral Gables, Coral Gables, Florida, United States
- UM Sylvester Comprehensive Cancer Center at Deerfield Beach, Deerfield Beach, Florida, United States
- University of Miami Miller School of Medicine-Sylvester Cancer Center, Miami, Florida, United States
- University of Kansas Clinical Research Center, Fairway, Kansas, United States
- HaysMed, Hays, Kansas, United States
- University of Kansas Cancer Center, Kansas City, Kansas, United States
- Lawrence Memorial Hospital, Lawrence, Kansas, United States
- The University of Kansas Cancer Center - Olathe, Olathe, Kansas, United States
- University of Kansas Cancer Center-Overland Park, Overland Park, Kansas, United States
- University of Kansas Hospital-Indian Creek Campus, Overland Park, Kansas, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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