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Clinical Trial Summary

The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-B01D1 in patients with Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors.


Clinical Trial Description

BL-B01D1-LUNG-101 is a global, multi-center, Phase 1 study to evaluate the safety, tolerability, pharmacokinetics , and initial efficacy of BL-B01D1 in participants with metastatic or unresectable NSCLC and Other Solid Tumors. This study will be conducted in two different dosing schedules (Cohort A and Cohort B) and three parts (dose escalation, dose finding and dose expansion). Cohort A will be dosed on Day 1 and Day 8 of a continuous 21-day treatment cycle. Cohort B will be dosed on Day 1 of a continuous 21-day treatment cycle. Each Cohort has different dose groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05983432
Study type Interventional
Source SystImmune Inc.
Contact Ta Barrineau
Phone (425) 453-6841
Email tara.barrineau@systimmune.com
Status Recruiting
Phase Phase 1
Start date August 8, 2023
Completion date September 30, 2025

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