A Multicenter, Open-label, Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of LBL-034 in Patients With Relapsed/Refractory Multiple Myeloma
Latest Information Update: 06 Dec 2025
At a glance
- Drugs LBL 034 (Primary)
- Indications Multiple myeloma
- Focus Adverse reactions; First in man; Therapeutic Use
- Sponsors Nanjing Leads Biolabs
Most Recent Events
- 25 Aug 2025 According to a media release, 50 patients have been treated at dose levels up to 1200 ug/kg in the dose-escalation and expansion phase 1 trial evaluating the therapy for relapsed or refractory multiple myeloma (MM).
- 25 Aug 2025 According to a Nanjing Leads Biolabs media release, today announced the first patient has been successfully dosed in the Phase II trial of LBL-034 following strong Phase I data.
- 13 May 2025 Planned number of patients changed from 418 to 342.