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NCT03065790

Early FDG PET/CT Imaging as a Measure of Response in Patients With Non-Hodgkin Lymphoma on Lenalidomide

Terminated Last updated 4 June 2021
What this trial tests

trial testing 2-Deoxy-2-[18F]fluoro-D-glucose (FDG) in Non-Hodgkin Lymphoma in 1 participant. Terminated before completion.

Timeline
6 February 2017
Primary endpoint
28 April 2021
28 April 2021

Quick facts

Lead sponsorAbramson Cancer Center at Penn Medicine
StatusTerminated
Study typeOBSERVATIONAL
Enrollment1
Start date6 February 2017
Primary completion28 April 2021
Estimated completion28 April 2021
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abramson Cancer Center at Penn Medicine — full company profile →

Who can join

18 and older, any sex, with Non-Hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Adult patients with non-Hodgkin lymphoma who will be treated with lenalidomide will undergo FDG PET/CT scan as an early evaluation of response to therapy. Changes in FDG uptake will be correlated response and long term outcomes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Non-Hodgkin Lymphoma

Currently open trials in the same condition.

Other Abramson Cancer Center at Penn Medicine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03065790.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing