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OncoMatch/Clinical Trials/NCT05272826

Study of Iberdomide, Bortezomib, Dexamethasone With Isatuximab Added on Demand for ND-NTE MM Patients

Is NCT05272826 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Iberdomide and Bortezomib for multiple myeloma.

Phase 2RecruitingCanadian Myeloma Research GroupNCT05272826Data as of Jun 2026Location: Canada

Treatment: Iberdomide · Bortezomib · Dexamethasone · IsatuximabThis study will evaluate efficacy and tolerability of iberdomide, bortezomib, dexamethasone and isatuximab on demand administered in combination for newly diagnosed transplant-ineligible multiple myeloma patients.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Isatuximab

Targeted therapy

IberdomideBortezomib

Other

Dexamethasone

Cancer type

Multiple Myeloma

Performance status

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

Demographics

Ages ≥ 65

Prior therapy

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

Cannot have received: anti-myeloma therapy

Exception: does not include radiotherapy, bisphosphonates, or a single short course of steroid (≤ dexamethasone 40 mg/day for 4 days; not within 14 days of treatment start)

Previous treatment with anti-myeloma therapy (does not include radiotherapy, bisphosphonates, or a single short course of steroid [i.e. less than or equal to the equivalent of dexamethasone 40 mg/day for 4 days; such a short course of steroid treatment must not have been given within 14 days of treatment start])

Lab requirements

Blood counts

Absolute neutrophil count (ANC) ≥ 1.0 x 10^9/L; Platelet count ≥ 50 x 10^9/L; Hemoglobin ≥ 80 g/L

Kidney function

Creatinine clearance ≥ 30 mL/min either directly measured via 24-hour urine collection or calculated using MDRD

Liver function

Serum AST and ALT ≤ 1.5 x upper limit of normal (ULN)

Cardiac function

QTc interval < 470 msecs (QTcF); no evidence of current clinically significant uncontrolled arrhythmias; no history of MI, acute coronary syndromes, coronary angioplasty, stenting or bypass grafting within six months; no class III or IV heart failure (NYHA); no uncontrolled hypertension

Absolute neutrophil count (ANC) ≥ 1.0 x 10^9/L. Serum AST and ALT ≤ 1.5 x upper limit of normal (ULN). Creatinine clearance ≥ 30 mL/min...Platelet count ≥ 50 x 10^9/L...Hemoglobin ≥ 80 g/L...QTc interval ≥ 470 msecs...NYHA heart failure class III-IV...uncontrolled hypertension

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

Frequently asked questions

Is NCT05272826 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.

Could you qualify for this trial?

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

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