Clinical Trials Directory

Trials / Completed

CompletedNCT04856774

Trial of SHR-1701 Plus BP102 in Subjects With Selected Solid Tumors

A Multicenter, Open-Label, Phase Ib/II Trial of SHR-1701 Plus BP102 in Subjects With Selected Solid Tumors

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

Summary

The main purpose of this study was to assess the safety, tolerability, and efficacy when combining SHR-1701 and BP102 in participants with certain cancers. This study was conducted in 2 phases, Phase Ib and Phase II.

Conditions

Interventions

TypeNameDescription
DRUGSHR-1701;BP102Drug: SHR-1701 IV infusion Drug: BP102 IV infusion Phase Ib: SHR-1701 30mg/kg + BP102 15mg/kg Q3w as starting dose, until recommended phase 2 dose is determined.

Timeline

Start date
2021-06-01
Primary completion
2024-03-30
Completion
2024-03-30
First posted
2021-04-23
Last updated
2024-06-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04856774. Inclusion in this directory is not an endorsement.

Trial of SHR-1701 Plus BP102 in Subjects With Selected Solid Tumors (NCT04856774) · Clinical Trials Directory