CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 497 enrolled
Drug / intervention
BL-B01D1 +3 moredrug
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/NCT06304974
NCT06304974Phase 3Active

A Phase Ill Randomized Controlled Clinical Study Comparing BL-B01D1 With Chemotherapy of Physician's Choice as Second Line Treatment in Patients With Recurrent or Metastatic Esophageal Squamous Cell Carcinoma After Failure of PD-1/PD-L1 Monoclonal Antibody in Combination With Platinum-based Chemotherapy

Sichuan Baili Pharmaceutical Co., Ltd.·interventional·Posted Mar 12, 2024·Updated Apr 17, 2026

In Brief

A Phase 3 clinical trial evaluating BL-B01D1, Irinotecan, and 2 other interventions for Esophageal Squamous Cell Carcinoma. Active but no longer recruiting, targeting 497 participants across 1 site.

Detailed Summary

This study is a registered phase Ill, randomized, open-label, multicenter study to evaluate the efficacy and safety of BL-B01D1 in patients with recurrent or metastatic esophageal squamous cell carcinoma after failure of PD-1/PD-L1 monoclonal antibody in combination with platinum-based chemotherapy.

Study Details

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

Timeline

Phase 3ActiveOverdue
20252026
First PostedMar 12, 2024
Enrollment StartMar 19, 2024
Primary CompletionMay 1, 2026
TodayJul 1, 2026
Enrollment to primary: 2.1 yearsPosted 2.3 years ago

Interventions

BL-B01D1drug

Administration by intravenous infusion

Irinotecandrug

Administration by intravenous infusion

paclitaxeldrug

Administration by intravenous infusion

docetaxeldrug

Administration by intravenous infusion