Safety and Efficacy Study of An Anti-CD38 Antibody Drug Conjugate in Relapsed or Refractory Multiple Myeloma

This is a phase Ib/IIa, open-label, dose-escalation, and extension study to evaluate the safety and efficacy of an anti-CD38 antibody drug conjugate (STI-6129) in patients with relapsed or refractory multiple myeloma.

Trial Details

NCT ID
NCT05565807
Phase
PHASE1 / PHASE2
Sponsor
Zhejiang ACEA Pharmaceutical Co. Ltd.
Status
RECRUITING
Cancer Type
Multiple Myeloma
Interventions
  • STI-6129
Locations (sample)
  • Beijing, Beijing Municipality, China|39.9075,116.39723
  • Beijing, Beijing Municipality, China|39.9075,116.39723
  • Guangzhou, Guangdong, China|23.11667,113.25
  • Hangzhou, Zhejiang, China|30.29365,120.16142

Key Eligibility Criteria

  • Age ≥18 years old, regardless of gender.
  • Previously treated with at least three drugs (including PI, IMiD, and anti-CD38 antibody), and relapsed/refractory after the most recent anti-MM th…
  • Diagnosis of MM according to IMWG criteria with measurable lesions, meeting at least 1 of the following criteria:
  • Serum M protein ≥ 0.5g/dL (≥ 5 g/L); or

For full eligibility, visit ClinicalTrials.gov.

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