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OncoMatch/Clinical Trials/NCT05208307

Belantamab Mafodotin, Pomalidomide and Dexamethasone for the Treatment of High-Risk Myeloma

Is NCT05208307 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Belantamab Mafodotin and Dexamethasone for plasma cell myeloma.

Phase 2RecruitingEmory UniversityNCT05208307Data as of May 2026

Treatment: Belantamab Mafodotin · Dexamethasone · PomalidomideThis phase II trial studies the effect of belantamab mafodotin, pomalidomide, and dexamethasone in treating patents with high-risk myeloma. Belantamab mafodotin is a monoclonal antibody, called belantamab, linked to a chemotherapy drug, called mafodotin. Belantamab is a form of targeted therapy because it attaches to specific molecules on the surface of cancer cells, known as BCMA receptors, and delivers mafodotin to kill them. Chemotherapy drugs, such as pomalidomide, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Anti-inflammatory drugs, such as dexamethasone lower the body's immune response and are used with other drugs in the treatment of some types of cancer. Giving belantamab mafodotin, pomalidomide, and dexamethasone may kill more cancer cells.

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Biomarker criteria

Required: IGH t(14;16)

Required: IGH t(14;20)

Required: IGH t(4;14)

Required: TP53 deletion

Performance status

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

Prior therapy

Must have received: autologous stem cell transplant

has undergone autologous stem cell transplant (ASCT) within one year of their diagnosis and has achieved >= partial response (PR) based on IMWG standard criteria

Cannot have received: investigational drug or approved systemic anti-myeloma therapy (including systemic steroids)

Participant must not have used an investigational drug or approved systemic anti-myeloma therapy (including systemic steroids) within 14 days or five half-lives, whichever is shorter, preceding the first dose of study drug

Cannot have received: plasmapheresis

Participant must not have had plasmapheresis within 7 days prior to first dose of study treatment

Cannot have received: monoclonal antibody

Participant must not have received prior treatment with a monoclonal antibody within 30 days of receiving the first dose of study drugs

Cannot have received: major surgery

Participant must not have had major surgery =< 4 weeks prior to initiating study treatment

Lab requirements

Blood counts

ANC >=1.5 x 10^9/L; Hemoglobin >= 8.0 g/dL; Platelets >= 75 x 10^9/L

Kidney function

eGFR >= 30 mL/min/1.73 m^2; Spot urine (albumin/creatinine ratios) < 500 mg/g (56 mg/mmol)

Liver function

Total bilirubin =< 1.5 x ULN (Isolated bilirubin >= 1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%); ALT =< 2.5 x ULN

ANC >=1.5 x 10^9/L; Hemoglobin >= 8.0 g/dL; Platelets >= 75 x 10^9/L; Total bilirubin =< 1.5 x ULN (Isolated bilirubin >= 1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%); ALT =< 2.5 x ULN; eGFR >= 30 mL/min/1.73 m^2; Spot urine (albumin/creatinine ratios) < 500 mg/g (56 mg/mmol)

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

US trial sites

  • Emory University/Winship Cancer Institute · Atlanta, Georgia

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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