OncoMatch

OncoMatch/Clinical Trials/NCT06505369

Bispecific T-cell Redirectors as Part of First Line Treatment in Transplant Eligible Multiple Myeloma Patients

Is NCT06505369 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments for multiple myeloma.

Phase 2RecruitingNorth Estonia Medical CentreNCT06505369Data as of Jun 2026Location: Denmark · Estonia · Norway

Treatment: Daratumumab · Bortezomib · Lenalidomide · Dexamethasone · Talquetamab · TeclistamabThis is Phase 2, open-label, multicentre, non-randomised study evaluating participants with newly diagnosed MM eligible for high-dose therapy. The goal of the study is to determine if consolidation with T-cell redirectors - Talquetamab and Teclistamab in sequence will improve the response depth: increase MRD negative CR rate.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Immunotherapy

DaratumumabTalquetamabTeclistamab

Targeted therapy

Bortezomib

Endocrine / hormonal

Lenalidomide

Other

Dexamethasone

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 70

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic therapy or stem cell transplantation for any plasma cell dyscrasia

Exception: emergency use of a short course (equivalent of dexamethasone 40 mg/day for a maximum 4 days) of corticosteroids before treatment

Prior or current systemic therapy or stem cell transplantation for any plasma cell dyscrasia, with the exception of emergency use of a short course (equivalent of dexamethasone 40 mg/day for a maximum 4 days) of corticosteroids before treatment.

Lab requirements

Blood counts

Hemoglobin ≥8 g/dL; Platelets ≥75×10^9/L; ANC ≥1.0×10^9/L

Kidney function

eGFR ≥30 mL/min

Liver function

AST and ALT ≤2.5×ULN; Total bilirubin <1.5×ULN

Have clinical laboratory values meeting the following criteria: Hemoglobin ≥8 g/dL; Platelets ≥75×10^9/L; ANC ≥1.0×10^9/L; AST and ALT ≤2.5×ULN; eGFR ≥30 mL/min; Total bilirubin <1.5×ULN

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06505369 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 70 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify