Clinical trial · Interventional
MRD-Guided BCMA/CD3 Bispecific Antibody Treatment After Stem Cell Transplant for Newly Diagnosed Multiple Myeloma
A Prospective, Single-Arm Clinical Trial of MRD-Guided BCMA/CD3 Bispecific Antibody as Maintenance Therapy After Autologous Hematopoietic Stem Cell Transplantation in Newly Diagnosed Multiple Myeloma
NCT07409454CI-TRIAL-00120979CAREMM-007recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| anti-BCMA/CD3 bispecific antibody | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- BsAbs-treatment group
- interventionNames
- Drug: anti-BCMA/CD3 bispecific antibody
Primary outcomes (1)
- measure
- Minimal residual disease (MRD) negativity conversion rate
- timeFrame
- Up to 24 months
Secondary outcomes (4)
- measure
- Duration of MRD negativity
- timeFrame
- Up to 24 months
- measure
- Progression-Free Survival
- timeFrame
- From enrollment to the date of disease progression or death, up to approximately 24 months.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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 limited to first-line treatment only, including: (1) Induction therapy with a 3- or 4-drug regimen containing a proteasome inhibitor and/or an immunomodulatory drug and/or an anti-CD38 monoclonal antibody; (2) Single or tandem autologous stem cell transplantation (ASCT); (3) Up to 2-4 cycles of consolidation therapy post-ASCT are permitted, with the total number of induction plus consolidation cycles not exceeding 8. 6. Completion of ASCT within ≤12 months from the start of induction therapy; and ≤6 months from the most recent ASCT at enrollment (≤7 months if consolidation therapy was administered). 7. No prior maintenance therapy. 8. Achieved at least a partial response (≥PR) according to the IMWG 2016 response criteria. 9. Presence of measurable disease at diagnosis. Exclusion Criteria: 1. Prior treatment with genetically modified adoptive cellular therapy. 2. History of allogeneic stem cell transplantation or solid organ transplantation. 3. Disease progression prior to enrollment (per IMWG 2016 response criteria), or presence of plasma cell leukemia, Waldenström macroglobulinemia, POEMS syndrome, or light-chain amyloidosis not attributable to symptomatic multiple myeloma. 4. Central nervous system involvement.
References
Publications (0)
Data not yet available
No reference posted for this study.