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NCT04388371

Glutamine PET Imaging in LAM

Completed Phase 1 Last updated 11 August 2021
What this trial tests

Phase 1 trial testing Glutamine in Lymphangioleiomyomatosis (LAM) in 5 participants. Completed in 10 August 2021.

Timeline
18 October 2019
Primary endpoint
30 June 2021
10 August 2021

Quick facts

Lead sponsorVanderbilt University Medical Center
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment5
Start date18 October 2019
Primary completion30 June 2021
Estimated completion10 August 2021
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Vanderbilt University Medical Center

Who can join

18 and older, female only, with Lymphangioleiomyomatosis (LAM). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this study, subjects with spontaneous or tuberous sclerosis complex associated lymphangioleiomyomatosis (LAM) who have not been started on therapy with mTOR inhibitors such as sirolimus or everolimus to undergo a PET/CT scan using an novel PET tracer that may better evaluate disease activity in LAM subjects both before and after the initiation of mTOR inhibitor therapy will be enrolled. The procedure for each scan will be similar, involving one administration of the novel tracer C11-glutamine followed by a whole body PET/CT scan.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Glutamine

Trials testing the same drug.

Other recruiting trials for Lymphangioleiomyomatosis (LAM)

Currently open trials in the same condition.

Other Vanderbilt University Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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