Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06703177

A Study of SHR-1826 for Injection in Combination With Other Antitumor Therapies in Subjects With Solid Tumors

Phase IB/II Study of Safety, Tolerability and Efficacy of SHR-1826 for Injection in Combination With Other Antitumor Therapies in Subjects With Solid Tumors

Status
Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
876 (estimated)
Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is an open label, multi-center, multiple dose Phase IB/II study to evaluate the safety, tolerability and efficacy of SHR-1826 for injection in subjects with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
DRUGSHR-1826SHR-1826
DRUGSHR-4642SHR-4642
DRUGSHR-9839SHR-9839
DRUGSHR-8068SHR-8068
DRUGBevacizumab InjectionBevacizumab Injection
DRUGFluorouracil InjectionFluorouracil Injection
DRUGCalcium Folinate InjectionCalcium Folinate Injection
DRUGAdebrelimab InjectionAdebrelimab Injection
DRUGCapecitabine tabletsCapecitabine tablets, oral.

Timeline

Start date
2025-02-18
Primary completion
2026-01-01
Completion
2027-07-01
First posted
2024-11-25
Last updated
2025-12-03

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06703177. Inclusion in this directory is not an endorsement.