- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06994117
- Original Trial
Expanded Access for Mezigdomide
December 10, 2025 updated by: Bristol-Myers Squibb
This is an expanded access designed to provide access to Mezigdomide for eligible participants.
Study Overview
Status
Available
Intervention / Treatment
Study Type
Expanded Access
Expanded Access Type
- Individual Patients
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Description
Inclusion Criteria:
-
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Bristol-Myers Squibb, Bristol-Myers Squibb
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
May 19, 2025
First Submitted That Met QC Criteria
May 19, 2025
First Posted (Actual)
May 29, 2025
Study Record Updates
Last Update Posted (Actual)
December 11, 2025
Last Update Submitted That Met QC Criteria
December 10, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- CA057-1024
- CA057-1070 (Other Identifier: BMS Protocol ID)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Mezigdomide
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CelgeneCompletedRenal ImpairmentUnited States
-
Bristol-Myers SquibbCompletedHepatic ImpairmentUnited States
-
Memorial Sloan Kettering Cancer CenterBristol-Myers Squibb; Johnson & JohnsonRecruitingMultiple MyelomaUnited States
-
Massachusetts General HospitalBristol-Myers Squibb; Kura Oncology, Inc.Not yet recruitingKMT2A-rearranged | NPM1-mutant Refractory or Relapsed AMLUnited States
-
Memorial Sloan Kettering Cancer CenterRecruitingAcute Myeloid Leukemia | Leukemia | Acute Lymphoblastic Leukemia | Acute Leukemia | Refractory Leukemia | Refractory Acute Leukemia | Mixed Phenotype Acute Leukemia | Relapse LeukemiaUnited States
-
Juno Therapeutics, Inc., a Bristol-Myers Squibb...Recruiting
-
K36 Therapeutics, Inc.Bristol-Myers SquibbRecruitingMultiple Myeloma | Myeloma | Myeloma MultipleUnited States, France, Spain, Canada
-
Massachusetts General HospitalCelgene Corporation; Janssen Research and Development LLCRecruitingRelapsed Refractory Multiple Myeloma (RRMM)United States
-
CelgeneTerminatedMultiple MyelomaUnited States, Canada, Denmark, Australia, Belgium, Finland, Greece, Japan, Spain, United Kingdom, South Korea
-
CelgeneTerminatedMultiple MyelomaUnited States, Israel