Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma
2 other identifiers
interventional
111
1 country
1
Brief Summary
To learn more about the usefulness of molecular testing with the Molecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable lymphoma
Started Jul 2022
Typical duration for not_applicable lymphoma
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 7, 2022
CompletedFirst Submitted
Initial submission to the registry
July 12, 2022
CompletedFirst Posted
Study publicly available on registry
July 19, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 12, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 12, 2027
March 4, 2026
March 1, 2026
4.8 years
July 12, 2022
March 2, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Percentage of participants who have genomic test results available in <=7 days
through study completion an average of 1 year
Study Arms (1)
Molecular Testing
OTHERMolecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.
Interventions
Participants will be asked to allow previously-collected tumor tissue to be used for the MF Portrait test
Eligibility Criteria
You may qualify if:
- Male/female patients who are at least 18 years of age on the day of informed consent signing.
- Patients must have a histologically documented diffuse large B-cell lymphoma requiring therapy.
- Provision of written informed consent for the study.
You may not qualify if:
- \. None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
M D Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jason Westin, MD
M.D. Anderson Cancer Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 12, 2022
First Posted
July 19, 2022
Study Start
July 7, 2022
Primary Completion (Estimated)
May 12, 2027
Study Completion (Estimated)
May 12, 2027
Last Updated
March 4, 2026
Record last verified: 2026-03