drugset / Trial / NCT05150457

Safety and Preliminary Efficacy of BNA035 in Patients With Advanced Solid Tumors

NCT05150457 ↗

Phase 1 Unknown 48 enrolled Binacea Pharma, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of the study is to evaluate the safety and tolerability of BNA035 in order to determine the maximum tolerated dose (MTD) and Recommended Phase 2 dose (RP2D) and to evaluate the preliminary efficacy for each combination regimen.

Timeline

Start
2022-02-08
Primary completion
2023-11
Completion
2025-11

Drugs

EvaluationDrugModalityDoseRoute
Subject BNA035 Unknown — Intravenous