CI

At a glance

ClinicalIndex Comparison Record
Phase 1Recruiting· 96 target
Drug / intervention
BL-B01D1drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05262491
NCT05262491Phase 1RecruitingHigh MomentumUpdated 9mo ago
Long Recruiting

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of BL-B01D1 in Patients With Locally Advanced or Metastatic Gastrointestinal Tumor and Other Solid Tumor

Sichuan Baili Pharmaceutical Co., Ltd.·interventional·Posted Mar 2, 2022·Updated Sep 26, 2025

In Brief

A Phase 1 clinical trial evaluating BL-B01D1 for Gastrointestinal Tumor. Currently recruiting, targeting 96 participants across 6 sites.

Signals

Enrolling ahead of pace

Detailed Summary

In phase Ia study, the safety and tolerability of BL-B01D1 in patients with locally advanced or metastatic gastrointestinal tumor and other solid tumor will be investigated to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) of BL-B01D1. In phase Ib study, the safety and tolerability of BL-B01D1 at the phase Ia recommended dose will be further investigated, and recommended phase II dose (RP2D) for phase II clinical studies will be determined. In addition, the preliminary efficacy, pharmacokinetic characteristics, and immunogenicity of BL-B01D1 in patients with locally advanced or metastatic gastrointestinal tumor and other solid tumor will be evaluated.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina

Timeline

Phase 1Recruiting
2022202320242025202620272028
First PostedMar 2, 2022
Enrollment StartFeb 14, 2022
Primary CompletionDec 1, 2026
Study CompletionDec 1, 2027
TodayJul 1, 2026
Enrollment to primary: 4.8 yearsPosted 4.3 years agoPrimary completion in 5 months

Interventions

BL-B01D1drug

Administration by intravenous infusion