Clinical Trials Directory

Trials / Terminated

TerminatedNCT03379259

Study of BGB-A333 Alone and in Combination With Tislelizumab in Advanced Solid Tumors

Phase 1-2 Study Investigating Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of Anti-PD-L1 Monoclonal Antibody BGB-A333 Alone and in Combination With Anti-PD-1 Monoclonal Antibody Tislelizumab in Patients With Advanced Solid Tumors

Status
Terminated
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
39 (actual)
Sponsor
BeiGene · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

BGB-A333 is a humanized IgG1-variant monoclonal antibody against programmed cell death 1-ligand 1 (PD-L1), the ligand of an immune check point- receptor, programmed cell death-1 (PD-1). BGB-A317 is a humanized, IgG4-variant monoclonal antibody against PD-1. This study tested the safety and anti-tumor effect of BGB-A333 alone and in combination with BGB-A317 in participants with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
DRUGBGB-A333Anti-PD-L1 antibody
DRUGBGB-A317Anti-PD-1 antibodies

Timeline

Start date
2017-11-27
Primary completion
2020-09-08
Completion
2020-09-08
First posted
2017-12-20
Last updated
2024-10-26
Results posted
2021-11-09

Locations

8 sites across 3 countries: Australia, New Zealand, Spain

Source: ClinicalTrials.gov record NCT03379259. Inclusion in this directory is not an endorsement.

Study of BGB-A333 Alone and in Combination With Tislelizumab in Advanced Solid Tumors (NCT03379259) · Clinical Trials Directory