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Completed Phase 1 Interventional Results available

The Safety, Pharmacokinetics and Antitumor Activity of BGB-A317 in Combination With BGB-290 in Participants With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT02660034

Public ClinicalTrials.gov record NCT02660034. 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 Jul 22, 2026, 2:32 PM EDT

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

Official title

A Phase 1/1b, Open Label, Multiple Dose, Dose Escalation and Expansion Study to Investigate the Safety, Pharmacokinetics and Antitumor Activity of the Anti-PD-1 Monoclonal Antibody BGB-A317 in Combination With the PARP Inhibitor BGB-290 in Subjects With Advanced Solid Tumors

Study identification

NCT ID
NCT02660034
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
BeiGene
Industry
Enrollment
229 participants

Conditions and interventions

Conditions

Interventions

  • Tislelizumab Biological
  • Pamiparib Drug

Biological · Drug

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
Feb 1, 2016
Primary completion
Sep 8, 2020
Completion
Sep 8, 2020
Last update posted
Dec 5, 2021

2016 – 2020

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Pinnacle Oncology Hematology Scottsdale Arizona 85258
Cedars Sinai Medical Center Los Angeles California 90048
Rocky Mountain Cancer Centers Denver Colorado 80218
Mount Sinai Comprehensive Cancer Center Miami Beach Florida 33140
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Roswell Park Cancer Institute Buffalo New York 14263
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Sarah Cannon Research Institute Nashville Tennessee 37203
Vanderbilt University Medical Center Nashville Tennessee 37232
Texas Oncology Dallas Texas 75246
Texas Oncology Tyler Texas 75702
Virginia Cancer Specialists Fairfax Virginia 22031

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02660034, 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 Dec 5, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02660034 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →