RecruitingPhase 2NCT07096778

Inobrodib, Pomalidomide and Dexamethasone in Relapsed or Refractory Multiple Myeloma

A Phase II, Open-Label, Multicenter Study of Inobrodib in Combination With Pomalidomide and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma


Sponsor

CellCentric Ltd.

Enrollment

100 participants

Start Date

Jan 22, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to learn more about the anti-cancer activity of inobrodib, when given in combination with pomalidomide and dexamethasone, in patients with multiple myeloma that has come back following treatment and which no longer responds to available therapies. The study treatment will not be compared to any other treatment and patients will know what treatment they are receiving. This study will also further explore the side effects of inobrodib in combination with these other medicines.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new three-drug combination — inobrodib, pomalidomide, and dexamethasone — in people with multiple myeloma (a type of blood cancer) that has come back or stopped responding to prior treatments. Inobrodib is a new type of drug called a p300/CBP bromodomain inhibitor, which works differently from existing myeloma therapies. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with multiple myeloma that has relapsed or not responded to your last treatment - You are in reasonably good physical health (ECOG 0–2) - Your blood counts, kidney function, and liver function are at acceptable levels - You are willing to use reliable contraception if sexually active **You may NOT be eligible if...** - You have received another investigational or cancer drug within the past 14 days (or 30 days for antibody therapies) - You have previously been treated with a p300/CBP bromodomain inhibitor - You have a known severe allergy to inobrodib, pomalidomide, dexamethasone, or related immunomodulatory drugs (e.g., lenalidomide, thalidomide) - You have had major surgery or a live vaccine within 4 weeks of starting the study - 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

DRUGInobrodib

20 mg orally twice daily (b.i.d.) 4 days on / 3 days off for each 28-day cycle.

DRUGPomalidomide

4 mg orally once daily on Day 1 to 21 of each 28-day cycle

DRUGDexamethasone

40 mg orally once daily on Days 1, 8, 15 and 22 for each 28-day cycle


Locations(11)

Winship Cancer Institute

Atlanta, Georgia, United States

American Oncology Partners, PA

Bethesda, Maryland, United States

University of Nebraska Medical Center

Omaha, Nebraska, United States

University of Pennsylvania, Abramson Cancer Center

Philadelphia, Pennsylvania, United States

The Christie NHS Foundation Trust

Withington, Greater Manchester, United Kingdom

Royal Marsden NHS Foundation Trust

Sutton, London, United Kingdom

The Clatterbridge Cancer Centre NHS Foundation Trust

Bebington, Wirral, United Kingdom

Western General Hospital

Edinburgh, United Kingdom

Barts Health NHS Trust

London, United Kingdom

King's College Hospital NHS Foundation Trust

London, United Kingdom

Imperial College Healthcare NHS Trust, Hammersmith Hospital

London, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT07096778


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