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A Study to Investigate Tislelizumab (BGB-A317) Versus Placebo in Combination With Concurrent Chemoradiotherapy in Participants With Localized Esophageal Squamous Cell Carcinoma

Completed · Phase 3 · NCT03957590

Conditions: Esophageal Squamous Cell Carcinoma (ESCC)

At a glance

Research payments reported, 2025
$9,000
U.S. investigators named
3
Sites paid
3
Planned or actual enrollment
370

About the trial

Sponsor
BeiGene
Tested
Tislelizumab (drug), Placebo (drug), Paclitaxel (drug), Cisplatin (drug), Radiotherapy (radiation)
Dates
Started 2019-06-11; completion 2025-03-31
Results posted
Yes

This is a phase 3, randomized, double-blind, placebo-controlled study to compare the efficacy and safety of tislelizumab (BGB-A317) versus placebo in combination with chemoradiotherapy in participants with localized esophageal squamous cell carcinoma (ESCC).

From ClinicalTrials.gov, last updated 2026-04-13. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beigene, Ltd. reported $9,000 in research payments for this study in 2025 (9 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

  • Sbq Radiology, PLLC $4,965
  • Mgpo Radiology Associates $3,535
  • Scientia Imaging, LLC $500

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