Phase 2 Myeloma Trial, Recruiting NCT07096778 Sponsor: CellCentric Ltd. Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT07096778
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are 18 years of age or older, of any sex
  • People who have been diagnosed with multiple myeloma (a type of blood cancer) according to established medical guidelines, and whose cancer has come back or stopped responding to their most recent treatment
  • People whose general health and ability to carry out daily activities falls within a certain range, as measured by a standard health scoring system called the ECOG scale (scores 0 to 2, meaning fully active to capable of self-care)
  • People whose blood counts, kidney function, and liver function meet the required levels
  • People who are willing to use highly effective contraception with all sexual partners if they are sexually active

Who may not be able to join:

  • People who have received an experimental treatment, chemotherapy, immunotherapy, or another anticancer treatment from a previous clinical study within 14 days or 5 half-lives before the first dose, whichever is the shorter period; or who have received any antibody-based cancer therapy within 30 days
  • People who have previously been treated with a specific class of drugs called p300/CBP bromodomain inhibitors (confirm with trial site)
  • People with known or suspected serious allergies to any ingredients in the study medications — inobrodib, pomalidomide, or dexamethasone — or to similar drugs used in the past, such as lenalidomide or thalidomide
  • People taking medications, herbal supplements, or consuming foods that could interfere with how the study drugs work in the body (for example, strong CYP3A4 inducers or inhibitors — confirm with trial site)
  • People who have had major surgery within 4 weeks before the first dose of the study treatment
  • People who have received a live vaccine within 4 weeks before starting the study treatment
  • People who still have active or unresolved side effects from previous treatments
  • People who have had another active cancer (other than multiple myeloma) that was progressing or required a change in treatment within the last 24 months
  • People who are pregnant or breastfeeding at any point during the study
  • People with any other illness or medical history that could affect safety, the ability to follow the study requirements, or the ability for researchers to interpret the study results

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 14 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Naseer Qayum, CellCentric Ltd.

Phone: +44 1799 531130

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
CellCentric Ltd.
Registry
ClinicalTrials.gov
Start date
22 January 2026
Est. completion
1 December 2029

Where this trial is recruiting

🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Objective Response Rate, defined as the percentage of patients with a confirmed partial response (PR) or better, based on IMWG criteria and assessed by Independent Review Committee (IRC)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov