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Clinical Trials/NCT05968417
NCT05968417RecruitingNot Applicable

Investigation of the Activity of Novel Compounds for the Treatment of Myeloma and Mechanisms of Drug Resistance to Current Therapies

Institute of Cancer Research, United Kingdom1 site in 1 country250 target enrollmentStarted: July 22, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
250
Locations
1
Primary Endpoint
Cell viability

Study Overview

Brief Summary

Myeloma is a bone marrow cancer with over 5000 patients diagnosed in the UK each year. Researchers are committed to improving understanding of myeloma and developing more effective treatments with fewer side effects in order to improve patient outcomes. In order to do this, researchers are collecting samples of blood and bone marrow to test the activity of potential new treatments in the laboratory and to understand what may be the cause of some treatments not working.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Participants who have a diagnosis, or suspected diagnosis, of myeloma or related plasma cell disorder
  • Participants who are undergoing a peripheral blood or bone marrow aspirate sampling for diagnostic, staging or follow-up purposes, before, whilst or after receiving anti-myeloma treatment
  • Participants aged 18 years of age or above
  • Participants willing to consent to an additional sample being taken at the time of their peripheral blood or bone marrow aspirate sampling

Exclusion Criteria

  • Participants unable to provide consent
  • Participants with known active infectious diseases (e.g. HIV, Hepatitis B/C, COVID) that pose a risk to the use of the sample in the laboratory

Outcomes

Primary Outcomes

Cell viability

Time Frame: 12 months

Myeloma cell viability when incubated with standard of care and novel compounds.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Institute of Cancer Research, United Kingdom
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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