RecruitingPhase 1Phase 2NCT06876142

Combination Therapy (Mirdametinib and Sirolimus) for RAS Mutated Relapsed Refractory Multiple Myeloma

A Phase 1b/2 Study of Combination Therapy (Mirdametinib and Sirolimus) for RAS Mutated Relapsed Refractory Multiple Myeloma (RRMM)


Sponsor

National Cancer Institute (NCI)

Enrollment

54 participants

Start Date

Mar 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Background: Multiple myeloma (MM) is a type of blood cancer that affects a person s immunity. MM returns after treatment (relapse) in almost all people; MM may also not respond to initial treatment (refractory). Many people with relapsed refractory MM (RRMM) also have changes in their KRAS and NRAS genes. Researchers want to try a new drug treatment that targets cancer with these changed genes. Objective: To test 2 drugs (mirdametinib and sirolimus) in people with RRMM. Eligibility: People aged 18 and older with RRMM who have changes in their KRAS or NRAS genes. Design: Participants will be screened. They will have blood tests and imaging scans. They will have an eye exam and a test of their heart function. They will need to provide proof of their disease status and of their KRAS or NRAS status. If neither is available, the tests will be repeated. Participants will have a bone marrow biopsy: A needle will be inserted into a hipbone to draw out some soft tissue. This study will be done in two parts. In the first part of this study, we will find a safe dose of mirdametinib combined with sirolimus. In the second part, we will learn more about how mirdametinib combined with sirolimus may work against RRMM. Mirdametinib (capsules) and sirolimus (tablets) are taken by mouth. Participants will take both drugs at home on a 4-week cycle. They will take mirdametinib twice a day for the first 3 weeks of each cycle. They will take sirolimus once a day, every day, during each cycle. Participants will have study visits once a week during the first cycle, and then on the first day of subsequent cycles. Blood, heart, imaging scans, and other tests will be repeated. Treatment with the study drugs will go on for 1 year. Then participants will have follow-up visits every 3 months for 4 more years.


Eligibility

Min Age: 18 YearsMax Age: 120 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two drugs — mirdametinib (a drug that blocks a cancer signaling pathway) and sirolimus (an immunosuppressant used to block a different pathway) — in people with relapsed or treatment-resistant multiple myeloma who have a specific RAS gene mutation. **You may be eligible if...** - You have been diagnosed with multiple myeloma confirmed by international criteria - Your cancer has a documented RAS mutation - Your cancer has returned or is no longer responding after multiple prior treatments - You have adequate organ function **You may NOT be eligible if...** - You have not exhausted standard treatments that you are eligible for - You have uncontrolled infections or other significant active medical conditions - You have brain involvement from myeloma - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGMirdametinib

Capsules taken by mouth twice a day (2-12mg) for days 1-21 days of each 28 day cycle

DRUGSirolimus

Tablets taken by mouth once a day for days 1-28 days of each 28 day cycle. Loading dose of 12 mg on Day 1 Cycle 1 with 4 mg being taken for the remaining doses.


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT06876142


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