MRD-Guided BCMA/CD3 Bispecific Antibody Treatment After Stem Cell Transplant for Newly Diagnosed Multiple Myeloma

Recruiting Phase 2 Interventional Study
Multiple Myeloma
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
Institute of Hematology & Blood Diseases Hospital, China · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

This is a prospective, single-arm clinical study designed to evaluate the efficacy and safety of the BCMA/CD3 bispecific antibody (CM336) as maintenance therapy after autologous hematopoietic stem cell transplantation in patients with newly diagnosed multiple myeloma.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: 1. Be able to understand and voluntarily signs the informed consent form (ICF). 2. Age ≥ 18 years. 3. Newly diagnosed multiple myeloma according to the International Myeloma Working Group (IMWG) criteria. 4. MRD positivity (≥10-⁵) detected by EuroFlow. 5. Previous therapy limite…
Contacts

An Gang, PhD&MD

86-022-23909171

angang@ihcams.ac.cn

CONTACT