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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

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Trial Profile

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

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 09 Jun 2025

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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

  • 13 May 2025 Planned number of patients changed from 418 to 342.
  • 06 Nov 2024 According to a Nanjing Leads Biolabs media release, The preliminary data from this study will be presented at the 66th ASH Annual Meeting in San Diego, USA in December 9, 2024.
  • 27 Oct 2023 Status changed from not yet recruiting to recruiting.

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