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CoMMit to CURES.

At CoMMit, our MISSION is to reduce the burden of multiple myeloma by aggregating investigators, patients, and private entities to develop better therapies through efficient, and patient-centered clinical trials

400+

Engaged Patients

30+

Dedicated Researchers

15+

Myeloma Centers of Excellence

10+

Years of Impact

ACTIVE RESEARCH

MASTER-2 Trial

The MASTER-2 trial pioneers the use of measurable residual disease (MRD) to modulate type and intensity of therapy for patients with newly diagnosed multiple myeloma. This trial studies deferral of transplantation for patients who achieve MRD negativity, the use of an anti-BCMA bispecific T-cell engager for patients MRD positive, and MRD-guided fixed duration therapy.

FASTER Trial

The FASTER trial studies whether a combination of anti-CD38 antibody and an BCMA-directed bispecific T-cell engager can outperform autologous stem cell transplantation and anti-CD38 antibody plus lenalidomide maintenance in patients with newly diagnosed multiple myeloma.

IMPEDE Trial

The IMPEDE trial explores the concomitant use of anti-CD38 and anti-SLAMF7 monoclonal antibodies in combination with pomalidomide for treatment of relapsed and refractory multiple myeloma

COMMANDER Trial

The COMMANDER trial explores combinations with Iberdomide, an oral agent belonging to a new class of drugs, the CELMoDs, with the objective to eliminate measurable residual disease (MRD) in patients who completed autologous stem cell transplantation.

Publications

By running clinical trials with limited duration of therapy, we could describe the patterns of immune reconstitution after treatment cessation.

We used next-generation sequencing to quantify myeloma disease burden before and after autologous stem cell transplantations providing a benchmark to study immunotherapeutic alternatives to transplantation.

A panel of CoMMit experts put together a number of practical recommendations to reduce the impact of infections in the outcomes of patients with MM receiving bispecific antibodies or CAR T-cells.

Using data from MASTER enriched by a real-world dataset we framed the concept of “MRD-P”, the increase in MRD burden without traditional criteria for progression and describe its prognostic implication.

In another collaboration with GRIFFIN investigators, we describe the success of stem cell mobilization after quadruplet therapy.

We collaborated with investigators from the GRIFFIN trial to join data from GRIFFIN + MASTER and describe the outcomes of patients with high-risk myeloma treated with quadruplet therapy and autologous stem cell transplantation.

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YOUR DONATION IS THE FUEL THAT ADVANCES MYELOMA CURES.

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