Skip to main content
Clinical Trials/NCT05464823
NCT05464823Active, not recruitingNot Applicable

Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma

M.D. Anderson Cancer Center1 site in 1 country111 target enrollmentStarted: July 7, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
111
Locations
1
Primary Endpoint
Percentage of participants who have genomic test results available in <=7 days

Study Overview

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.

Detailed Description

Primary Objective:

• To determine the feasibility and turnaround of clinical WES and transcriptome sequencing

Secondary Objectives:

  • To determine the frequency of actionable DNA and RNA alterations
  • To determine the concordance of DNA and RNA alterations
  • To determine the frequency of molecularly matched therapy
  • To determine the feasibility of identifying mechanism(s) of acquired resistance with genomic profiling
  • To determine the feasibility of molecularly matched therapy to acquired resistance alterations

Exploratory Objectives:

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patient Eligibility:
  • Inclusion Criteria:
  • 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.

Exclusion Criteria

  • Not provided

Arms & Interventions

Molecular Testing

Other

Molecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.

Intervention: Molecular Functional Portrait (Other)

Outcomes

Primary Outcomes

Percentage of participants who have genomic test results available in <=7 days

Time Frame: through study completion an average of 1 year

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials