drugset / Trial / NCT03579836

Evaluation of Safety and Efficacy in BEY1107 in Monotherapy Gemcitabine Combination in Patient with Pancreatic Cancer

NCT03579836

Phase 1/2 Recruiting 75 enrolled BeyondBio Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is a single center, open-label, non-comparative, phase I/II clinical trial to assess the maximum tolerated dose (MTD), safety and efficacy of BEY1107 in monotherapy and in combination with gemcitabine in patient With locally advanced or metastatic pancreatic cancer.

Timeline

Start
2018-05-14
Primary completion
2026-11-30
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject AVOTACICLIB Small molecule Oral
Subject Gemcitabine Small molecule 1000 mg/m2 Intravenous

Indications

No indication recorded.