A Phase Ib Study of HS-10370 in Addition to Other Anti-cancer Therapies in Patients With Advanced Solid Tumors

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

762

Participants

Timeline

Start Date

May 30, 2025

Primary Completion Date

December 31, 2028

Study Completion Date

April 30, 2030

Conditions
Advanced Solid TumorsColorectal CancerNon-Small Cell Lung Cancer
Interventions
DRUG

HS-10370

Participants will receive HS-10370 dose 1 administered orally

DRUG

HS-20117

Participants will receive HS-20117 given as dose 3 intravenous infusion(IV) once every 14-day cycle.

DRUG

Adebrelimab

Participants will receive Adebrelimab intravenous infusion(IV) once every 21-day cycle

DRUG

Capecitabine

Participants will receive Capecitabine administered orally

DRUG

Oxaliplatin

Participants will receive Oxaliplatin intravenous infusion(IV) once every 21-day cycle.

DRUG

Folinic Acid, Fluorouracil and Oxaliplatin/Irinotecan

Participants will receive Folinic Acid, Fluorouracil and Oxaliplatin/Irinotecan intravenous infusion(IV) once every 14-day cycle.

DRUG

HS-20093

Participants will receive HS-20093 intravenous infusion(IV) once every 21-day cycle

DRUG

platinum (cisplatin or carboplatin)

Participants will receive platinum (cisplatin or carboplatin) administered IV in 21-day cycles.

Trial Locations (2)

Unknown

The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou

Sun Yat-sen University Cancer Center, Shanghai

All Listed Sponsors
lead

Jiangsu Hansoh Pharmaceutical Co., Ltd.

INDUSTRY