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Completed Phase 1 Interventional Results available

Study of Ociperlimab (BGB-A1217) in Combination With Tislelizumab in Advanced Solid Tumors

ClinicalTrials.gov ID: NCT04047862

Public ClinicalTrials.gov record NCT04047862. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 5:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 1/1b Study Investigating Safety, Tolerability, PK and Antitumor Activity of Anti-TIGIT Monoclonal Antibody BGB-A1217 in Combination With Anti-PD-1 Monoclonal Antibody Tislelizumab in Patients With Advanced Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objectives of this study were: to assess the safety and tolerability, to determine the maximum tolerated dose (MTD) or maximum administered dose (MAD) and to determine the recommended Phase 2 dose (RP2D) of BGB-A1217 (known as ociperlimab) in combination with tislelizumab in participants with advanced solid tumors in phase 1. Primary objective of Phase 1b was to assess overall response rate (ORR) determined by Investigator per Response Evaluation Criteria in Solid Tumors (RECIST) version (v).1.1 for patients in each dose-expansion cohort.

Study identification

NCT ID
NCT04047862
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
BeiGene
Industry
Enrollment
446 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 15, 2019 (Actual)
Primary completion
Aug 7, 2024 (Actual)
Completion
Aug 7, 2024 (Actual)
Last update posted
Aug 22, 2025

2019 – 2024

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
Mayo Clinic Phoenix Phoenix Arizona 85254 —
Scri Florida Cancer Specialists South Fort Myers Florida 33901 —
Mayo Clinic Jacksonville Jacksonville Florida 32224 —
Scri Florida Cancer Specialists North St. Petersburg Florida 33705 —
University of Kansas Medical Center Research Institute Kansas City Kansas 66160 —
University of Minnesota Minneapolis Minnesota 55455 —
Mayo Clinic Rochester Rochester Minnesota 55905 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08901 —
Providence Portland Medical Center Portland Oregon 97213 —
Tennessee Oncology, Pllc Nashville Nashville Tennessee 37203 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04047862, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 22, 2025 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04047862 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →