Multi-cohort, Single-arm, Phase II Study of the Efficacy and Side Effects of Cisplatin Plus Gemcitabine in the Treatment of PD1 Failure or Intensive Treatment of Some Rare Tumors

PHASE2RecruitingINTERVENTIONAL
Enrollment

84

Participants

Timeline

Start Date

January 1, 2025

Primary Completion Date

July 31, 2026

Study Completion Date

July 31, 2028

Conditions
Advanced Solid Tumors
Interventions
COMBINATION_PRODUCT

cisplatin-based chemotherapy

Patients were required to have a creatinine clearance of more than 60 and to receive standard doses of cisplatin and gemcitabine (gemcitabine 1000mg /m2 on day 1.8 and cisplatin 70 mg /m2 on day 1, q3w). A total of 4-6 courses of treatment were performed.

Trial Locations (1)

200000

RECRUITING

Shanghai Cancer Center, Fudan University, Shanghai

All Listed Sponsors
lead

Sheng Zhang

OTHER