CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 570 target
Drug / intervention
BL-B01D1 +2 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/NCT06475300
NCT06475300Phase 2RecruitingOn Track

A Phase II Clinical Trial to Evaluate the Efficacy and Safety of BL-B01D1+PD-1 Monoclonal Antibody in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer, Nasopharyngeal Carcinoma and Other Solid Tumors

Sichuan Baili Pharmaceutical Co., Ltd.·interventional·Posted Jun 26, 2024·Updated May 6, 2026

In Brief

A Phase 2 clinical trial evaluating BL-B01D1, PD-1 Monoclonal Antibody, and 1 other intervention for Non-small Cell Lung Cancer and 2 related conditions. Currently recruiting, targeting 570 participants across 1 site.

Detailed Summary

This phase II study is a clinical study to explore the efficacy and safety of BL-B01D1 combined with PD-1 Monoclonal Antibody in patients with locally advanced or metastatic non-small cell lung cancer, nasopharyngeal carcinoma and other solid tumors.

Study Details

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

Timeline

Phase 2RecruitingOverdue
20252026
First PostedJun 26, 2024
Enrollment StartJun 25, 2024
Primary CompletionJul 1, 2026
TodayJul 1, 2026
Enrollment to primary: 2.0 yearsPosted 2.0 years ago

Interventions

BL-B01D1drug

Administration by intravenous infusion for a cycle of 3 weeks.

PD-1 Monoclonal Antibodydrug

Administration by intravenous infusion for a cycle of 3 weeks.

Pemetrexed Disodiumdrug

Administration by intravenous infusion for a cycle of 3 weeks.