A Study on Tuvusertib (Oral ATR Inhibitor) in Combination With PLX038 (Topo1 Inhibitor) in Patients With Advanced Solid Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

92

Participants

Timeline

Start Date

January 20, 2025

Primary Completion Date

September 23, 2028

Study Completion Date

September 23, 2029

Conditions
Solid Tumor
Interventions
DRUG

PLX038 + Tuvusertib

"Dose escalation will be conducted on the grid defined by the 4 doses of PLX038 (800 mg/m², 1000 mg/m², 1300 mg/m² and 1700 mg/m² IV every 21 days D1=D22) and 3 doses of Tuvusertib (90 mg, 130 mg and 180 mg QD for 10 days from D3, D3-12). Premedication with anti-emetic agents is not required prior to the initial infusion, but may be used for an individual patient, as needed.~All included patients will receive PLX038 + Tuvusertib until progression of disease, unacceptable toxicity, patient withdrawal of consent, investigator decision, lost to follow-up, death, patient non-compliance, or study termination by Sponsor."

Trial Locations (2)

75005

RECRUITING

Institut Curie, Paris

92210

NOT_YET_RECRUITING

Institut Curie, Saint-Cloud

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

ProLynx LLC

INDUSTRY

collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

Institut Curie

OTHER

NCT06337630 - A Study on Tuvusertib (Oral ATR Inhibitor) in Combination With PLX038 (Topo1 Inhibitor) in Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter