RecruitingPhase 2NCT06598787

A Study of BL-B01D1 in Patients With Recurrent Glioblastoma

A Phase II Clinical Study to Evaluate the Efficacy and Safety of BL-B01D1 for Injection in Patients With Recurrent Glioblastoma


Sponsor

Sichuan Baili Pharmaceutical Co., Ltd.

Enrollment

20 participants

Start Date

Oct 17, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is an open-label, multicenter, phase II study to evaluate the safety, efficacy, and pharmacokinetic characteristics of BL-B01D1 for Injection in patients with recurrent glioblastoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called BL-B01D1 (an antibody-drug conjugate) in patients with glioblastoma — the most aggressive form of brain cancer — that has come back after standard treatment. **You may be eligible if...** - You are 18 or older - You have confirmed recurrent glioblastoma after failing standard treatment - You have a Karnofsky performance score of 60 or above (able to care for yourself with some assistance) - Your expected survival is at least 3 months - Your blood counts, heart, and kidney function meet study requirements **You may NOT be eligible if...** - You received chemotherapy or immunotherapy within the past 4 weeks - You have serious heart conditions (arrhythmia, prolonged QT interval, heart failure) - You have active autoimmune or inflammatory disease - You have another active cancer - You have active HIV, tuberculosis, hepatitis B, or hepatitis C - You had a serious infection within the past 4 weeks - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBL-B01D1 for Injection

Administration by intravenous infusion for a cycle of 3 weeks.


Locations(1)

Beijing Tiantan Hospital, Capital Medical University

Beijing, Beijing Municipality, China

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NCT06598787


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