Skip to main content

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

Completed · Phase 1 · NCT04047862

Conditions: Locally Advanced and Metastatic Solid Tumors

At a glance

Research payments reported, 2025
$66,868
U.S. investigators named
9
Sites paid
6
Planned or actual enrollment
446

About the trial

Sponsor
BeiGene
Tested
Ociperlimab (drug), Tislelizumab (drug), Pemetrexed (drug), Paclitaxel (drug), Nab paclitaxel (drug), Carboplatin (drug), Cisplatin (drug), Etoposide (drug), 5fluorouracil (drug), Oxaliplatin (drug), Capecitabine (drug)
Dates
Started 2019-08-15; completion 2024-08-07
Results posted
Yes

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.

From ClinicalTrials.gov, last updated 2025-08-22. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines USA, Inc. reported $66,868 in research payments for this study in 2025 (21 payments).

Products named: Tevimbra

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.