A Study of CS1001 in Combination With Regorafenib in Patients With Advanced or Refractory Solid Tumors

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

December 13, 2019

Primary Completion Date

May 13, 2021

Study Completion Date

August 18, 2021

Conditions
Advanced Refractory Solid Tumors
Interventions
DRUG

CS1001

One course will last 28 days. CS1001 will be intravenously administered every 4 weeks (Q4W).

DRUG

Regorafenib

One course will last 28 days. Administration will be orally (p.o.) taken at different dose schemes.

Trial Locations (1)

5037

Ashford Cancer Centre Research, Kurralta Park

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bayer

INDUSTRY

lead

CStone Pharmaceuticals

INDUSTRY