Skip to main content

iberdomide

Generic: CC-220·Code: CC-220

iberdomide: 16 clinical trials tracked.

iberdomide evidence translation

What we can confirm

16 tracked trials

No verified listed developer

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 iberdomide, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 3 study sponsors
Clinical Trials (16)showing 10 most recent

Expanded Access for Iberdomide

Available
Expanded AccessBristol-Myers Squibb

Feasibility Study of Iberdomide (CC-220) Priming to Improve T Cell Fitness Prior to Leukapheresis for Chimeric Antigen Receptor T Cell (CAR-T) Therapy for Relapsed/Refractory Multiple Myeloma (RRMM)

NCT07727668·Early Phase 1
Not yet recruiting

Primary endpoint: Proportion of patients with T cell effector memory (TEM) expansion following iberdomide priming.

Interventionalopen22 targetStarted 2026-07Completion 2031-071 site · United StatesShambavi Richard

Determination 2 - Isatuximab, Iberdomide, Bortezomib and Dexamethasone Induction, Followed by Risk- and Response-Adapted Consolidation and Maintenance Therapy, in Transplant-Eligible Patients With Newly Diagnosed Multiple Myeloma

NCT07624513·Phase 3
Not yet recruiting

Primary endpoint: 3-Year Sustained Minimal Residual Disease (sMRD)-negative Complete Response (CR) Rate [Cohort 1] (Step 2)

InterventionalRandomizedopen720 targetStarted 2026-06Completion 2038-033 sites · United StatesDana-Farber Cancer Institute

Phase 1/2 Study of Etentamig in Combination With a CELMoD Agent for the Treatment of Patients With Relapsed/Refractory Multiple Myeloma

NCT06896916·Phase 1·ABBV
Recruiting

Primary endpoint: Phase 1: Dose-Limiting Toxicities (DLT)s of Etentamig when given in Combination with Iberdomide in Participants with Relapsed/Refractory Multiple Myeloma (RRMM)

Interventionalopen135 targetStarted 2025-08Completion 2036-0326 sites · Australia, Canada, France, Japan…AbbVie

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

NCT06892522·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

Isatuximab and Iberdomide as Immunotherapy for High Risk in Smouldering Myeloma

NCT06762769·Phase 2
Recruiting

Primary endpoint: Treatment deliverability, measured by treatment discontinuation before completion of 26 cycles

Interventionalopen63 targetStarted 2025-06Completion 2032-112 sites · United KingdomUniversity College, London

A Phase I/II Study of the Safety, Tolerability and Efficacy of Belantamab Mafodotin (GSK2857916) in Combination With Iberdomide (CC-220)/Dexamethasone Versus Belantamab Mafodotin (GSK2857916)/Dexamethasone in Relapsed Refractory Multiple Myeloma

NCT06232044·Phase 1/Phase 2
Recruiting

Primary endpoint: Maximum tolerated dose (MTD) of iberdomide (Phase I)

InterventionalRandomizedopen88 targetStarted 2025-04Completion 2030-0843 sites · United StatesAlliance for Clinical Trials in Oncology

A Randomized Phase III Trial Assessing Iberdomide Versus Iberdomide Plus Isatuximab Maintenance Therapy Post Autologous Hematopoietic Stem Cell Transplantation in Patients With Newly Diagnosed Multiple Myeloma

NCT06216158·Phase 3
Active, not recruiting

Primary endpoint: Demonstration of superiority of iberdomide plus isatuximab compared to iberdomide with respect to bone marrow minimal residual disease (MRD).

InterventionalRandomizedopen411 targetStarted 2024-04Completion 2029-0650 sites · Austria, GermanyUniversity of Heidelberg Medical Center

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

NCT06121843·Phase 1·BMY
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 1B, OPEN-LABEL STUDY OF ELRANATAMAB IN COMBINATION WITH IBERDOMIDE IN PARTICIPANTS WITH RELAPSED REFRACTORY MULTIPLE MYELOMA

NCT06215118·Phase 1·PFE
Recruiting

Primary endpoint: Part 1: Number of participants with dose limiting toxicity (DLT)

InterventionalRandomizedopen87 targetStarted 2024-02Completion 2028-0343 sites · Australia, Canada, United StatesPfizer