New cocktail of drugs takes on Hard-to-Treat myeloma
NCT ID NCT05372354
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This early-stage trial is testing several new drug combinations, including an experimental drug called CC-92480, in people with multiple myeloma that has come back or stopped responding to treatment. The main goals are to check safety and find the right doses. About 260 participants will be enrolled across multiple sites. If the combinations show promise, they could offer new options for controlling this blood cancer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CC-92480 (BMS-986348) combined with other drugs (tazemetostat, BMS-986158, trametinib, dexamethasone)
- What this could lead to
- If successful, this could point toward new treatment options for people with multiple myeloma that has stopped responding to standard therapies.
- What could go wrong
- This is an early-phase trial (Phase 1b/2a) with a small number of participants, so the results may not lead to a proven treatment. The drug combinations may cause side effects or fail to control the cancer.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 260 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2022
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Relapsed or refractory multiple myeloma (MM) and must: 1. Have documented disease progression during or after their last myeloma therapy. 2. For Part 1 Dose Finding: Be refractory to, intolerant to, or not a candidate for available, established therapies known to provide clinical benefit in MM; For Part 2 Dose Expansion: Be refractory to or have relapsed after the protocol specified number of prior lines of therapy that include an immunomodulatory drug (IMiD), a proteasome inhibitor, an anti-CD38 mAb, and a T-cell redirecting therapy (TRT, eg, a CAR-T or T-cell engaging bispecific treatment) unless the participant is not a candidate for TRT. * Must have measurable disease. * Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1. * Agree to follow the CC-92480 Pregnancy Prevention Plan (PPP). Exclusion Criteria: * Known active or history of central nervous system (CNS) involvement of MM * Plasma cell leukemia; Waldenstrom's macroglobulinemia; polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome; or clinically significant light-chain amyloidosis. * Impaired cardiac function or clinically significant cardiac disease * Previous SARS-CoV-2 infection within 14 days for asymptomatic or mild symptomatic infections or 28 days for severe/critical illness prior to Cycle 1 Day 1 (C1D1) * For Part 1: received prior therapy with CC-92480 * For Part 2: received prior therapy with CC-92480, tazemetostat, BMS-986158, or trametinib * Previously received allogeneic stem-cell transplant at any time or received autologous stem-cell transplant within 12 weeks of initiating study treatment * Received any of the following within 14 days prior to initiating study treatment: 1. Plasmapheresis 2. Major surgery 3. Radiation therapy other than local therapy for myeloma associated bone lesions 4. Use of any systemic anti-myeloma drug therapy * Used any investigational agents within 28 days or 5 half-lives (whichever is shorter) prior to initiating study treatment * COVID-19 vaccine within 14 days prior to C1D1 Other protocol-defined inclusion/exclusion criteria apply
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Get notified about this study
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
15 sites in 5 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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Alberta Health Services AHS - Foothills Medical Centre FMC
RECRUITINGCalgary, Alberta, T2N 5G2, Canada
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Churchill Hospital
RECRUITINGOxford, Oxfordshire, OX3 7LE, United Kingdom
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Dana-Farber Cancer Institute
RECRUITINGBoston, Massachusetts, 02215, United States
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Hospital Universitario 12 de Octubre
RECRUITINGMadrid, 28041, Spain
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Hospital Universitario Marques de Valdecilla
RECRUITINGSantander, 39008, Spain
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ICO - Hospital Germans Trias i Pujol
RECRUITINGBarcelona, 08026, Spain
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John Theurer Cancer Center at Hackensack UMC
RECRUITINGHackensack, New Jersey, 07601, United States
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Johns Hopkins Medicine - The Sidney Kimmel Comprehensive Cancer Center
RECRUITINGBaltimore, Maryland, 21287, United States
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Local Institution - 0001
WITHDRAWNLeicester, Leicestershire, LE1 5WW, United Kingdom
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Local Institution - 0014
WITHDRAWNLiverpool, Merseyside, L7 8YA, United Kingdom
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Memorial Sloan Kettering Cancer Center
RECRUITINGNew York, New York, 10021, United States
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NIHR UCLH Clinical Research Facility
RECRUITINGLondon, W1T 7HA, United Kingdom
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Oslo University Hospital
RECRUITINGOslo, Outside US and Canada, 0450, Norway
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The Christie NHS Foundation Trust
RECRUITINGManchester, Greater Manchester, M20 4BX, United Kingdom
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UAB Comprehensive Cancer Center
RECRUITINGBirmingham, Alabama, 35249, United States
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University Health Network UHN - Princess Margaret Hospital PMH
RECRUITINGToronto, Ontario, M5G 2M9, Canada
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University of Alberta - Cross Cancer Institute
RECRUITINGEdmonton, Alberta, T6G 1Z2, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Cheap blood count ratios eyed as window into Myeloma's inflammatory grip
- Can a t-cell engager rescue myeloma that outsmarted CAR-T?
- Can myeloma treatment work without steroids?
- Double-Drug attack on Hard-to-Treat lymphomas
- Banking blood and bone marrow to decode plasma cell disorders
- Which scan sees hidden myeloma better: PET or MRI?