A Clinical Trial of LBL-034 in Patients With Relapsed Refractory Multiple Myeloma

This trial is a single-arm, open-label, multicenter phase I/II clinical study of LBL-034 in patients with RRMM to evaluate the safety, tolerability, PK profile, immunogenicity and efficacy of LBL-034.

Trial Details

NCT ID
NCT06049290
Phase
PHASE1 / PHASE2
Sponsor
Nanjing Leads Biolabs Co.,Ltd
Status
RECRUITING
Cancer Type
Multiple Myeloma
Interventions
  • LBL-034 for Injection
Locations (sample)
  • Wuhu, Anhui, China|31.35259,118.42947
  • Beijing, Beijing Municipality, China|39.9075,116.39723
  • Xiamen, Fujian, China|24.47979,118.08187
  • Guangzhou, Guangdong, China|23.11667,113.25
  • Shenzhen, Guangdong, China|22.54554,114.0683

Key Eligibility Criteria

  • Agree to follow the trial treatment regimen and visit schedule, voluntarily enroll in the study, and sign the written informed consent form;
  • Age ≥ 18 years at the time of signing the informed consent;
  • Eastern Cooperative Oncology Group (ECOG) Performance Status Scale≤ 1;
  • Documentation of initial diagnosis of multiple myeloma according to IMWG diagnostic criteria,or according to the IMWG 2021 diagnostic criteria, the…

For full eligibility, visit ClinicalTrials.gov.

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