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mezigdomide

mezigdomide: 6 clinical trials tracked.

mezigdomide evidence translation

What we can confirm

6 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about mezigdomide, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 3 study sponsors
Clinical Trial Registry Records (6)

A Phase 1 Study of Menin-KMT2A Inhibitor Ziftomenib (KO-539) in Combination With Cereblon E3 Ligase Modulator Mezigdomide (CC-92480) in Adolescents and Adults With Relapsed or Refractory Acute Myeloid Leukemia (AML)

NCT07355335Registry updated 2026-10-08·Phase 1
Recruiting

Primary endpoint: Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

Interventionalopen24 targetStarted 2026-09Completion 2028-012 sites · United StatesMassachusetts General Hospital

Teclistamab and Mezigdomide for Relapsed/Refractory Multiple Myeloma

NCT07105059Registry updated 2026-08-17·Phase 1
Recruiting

Primary endpoint: Number of Participants With Dose Limiting Toxicity Assessed by CTCAE v5.0

InterventionalRandomizedopen18 targetStarted 2025-08Completion 2028-087 sites · United StatesMemorial Sloan Kettering Cancer Center

A Phase 1/2, Open-Label, Platform Study to Evaluate Safety and Efficacy of T Cell Engaging Bi/Tri-specific Antibodies in Subjects With MM

NCT06892522Registry updated 2026-07-21·Phase 1/Phase 2·ABBV
Recruiting

Primary endpoint: Number of Participants with Adverse Events (AE)s

InterventionalRandomizedopen602 targetStarted 2025-06Completion 2035-1234 sites · Australia, Israel, Japan, Norway…AbbVie

A Phase 1, Multicenter, Open-label Study to Evaluate the Safety and Preliminary Efficacy of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma and Determine the Recommended Dose for Each Add-on Investigational Component

NCT06121843Registry updated 2026-07-16·Phase 1
Recruiting

Primary endpoint: Incidence of adverse events (AEs)

Interventionalopen187 targetStarted 2024-02Completion 2028-0819 sites · Canada, United StatesJuno Therapeutics, Inc., a Bristol-Myers Squibb Company

A Phase 3, Two-stage, Randomized, Multicenter, Open-label Study Comparing Mezigdomide (CC-92480/BMS-986348), Carfilzomib, and Dexamethasone (MeziKD) Versus Carfilzomib and Dexamethasone (Kd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM): SUCCESSOR-2

NCT05552976Registry updated 2026-09-24·Phase 3·BMY
Active, not recruiting

Primary endpoint: Progression-free Survival (PFS)

InterventionalRandomizedopen606 enrolledStarted 2023-01Completion 2029-07204 sites · Argentina, Australia, Austria, Brazil…Bristol-Myers Squibb

A Phase 1b/2 Study of Selinexor (KPT-330) in Combination With Backbone Treatments for Relapsed/Refractory Multiple Myeloma and Newly Diagnosed Multiple Myeloma

NCT02343042Registry updated 2026-07-15·Phase 1/Phase 2·KPTI
Recruiting

Primary endpoint: Phase 1 (Dose-escalation): Maximum Tolerated Dose (MTD)

InterventionalRandomizedopen300 targetStarted 2015-10Completion 2027-0425 sites · Canada, United StatesKaryopharm Therapeutics Inc