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Safety and Preliminary Effectiveness of BGB-A445 in Combination With Tislelizumab in Participants With Advanced Solid Tumors
NCT04215978 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to assess the safety and tolerability of BGB-A445 alone and in combination with tislelizumab in participants with advanced solid tumors; and to determine the maximum tolerated dose(s) (MTD) or maximum administered dose(s) (MAD) and recommended Phase 2 doses (RP2D) of BGB-A445 alone and in combination with tislelizumab.
Conditions Studied
Interventions
- DRUG BGB-A445
- DRUG tislelizumab
Study Locations (20)
Victoria
- Monash Health — Clayton
- Peter Maccallum Cancer Centre — Melbourne
- Nucleus Network — Melbourne
Other
- University of Malaya Medical Centre — Kuala Lumpur
- Sarawak General Hospital — Kuching
- Auckland City Hospital — Auckland
California
- Valkyrie Clinical Trials — Los Angeles
- California Cancer Associates for Research & Excellence (cCARE) — San Diego
Queensland
- Pindara Private Hospital — Benowa
- Princess Alexandra Hospital — Brisbane
Shandong
- Jinan Central Hospital — Jinan
- Linyi Cancer Hospital — Linyi
Zhejiang
- Sir Run Run Shaw Hospital Zhejiang University School of Medicine — Hangzhou
- Zhejiang Cancer Hospital — Hangzhou
Pennsylvania
- UPMC Hillman Cancer Center (Univ Of Pittsburgh) — Pittsburgh
New South Wales
- Blacktown Cancer And Haematology Centre — Blacktown
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 204 participants |
| Start Date | 2020-01-30 |
| Est. Completion | 2025-01-24 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04215978
The ClinicalTrials.gov registry entry for NCT04215978 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 204 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BeiGene, which has 91 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Advanced Solid Tumor appearing as the primary indexed condition, and to 2 interventions — of which BGB-A445 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04215978 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Victoria, Other, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04215978 about?
NCT04215978 is a clinical study titled "Safety and Preliminary Effectiveness of BGB-A445 in Combination With Tislelizumab in Participants With Advanced Solid Tumors". The purpose of this study is to assess the safety and tolerability of BGB-A445 alone and in combination with tislelizumab in participants with advanced solid tumors; and to determine the maximum tolerated dose(s) (MTD) or maximum administered dose(s) (MAD) and recommended Phase 2 doses (RP2D) of BGB...
What is the current status of trial NCT04215978?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 204 participants. The study started on 2020-01-30. Estimated completion is 2025-01-24.
What conditions does trial NCT04215978 study?
This clinical trial studies the following conditions: Advanced Solid Tumor, Non Small Cell Lung Cancer, Head and Neck Squamous Cell Carcinoma (HNSCC), Nasopharyngeal Carcinoma (NPC). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04215978?
The interventions under investigation include: BGB-A445 (DRUG), tislelizumab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04215978?
This trial is sponsored by BeiGene, which has 91 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04215978 being conducted?
This trial has 20 study locations across California, Pennsylvania, New South Wales, Queensland, Victoria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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