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NCT03654794: DIFF-TAC

Study of the Cellular Diffusion of Tacrolimus Across the Membrane of Mononuclear Cells

Completed Last updated 4 September 2018
What this trial tests

trial testing Cell pharmacokinetics of tacrolimus in Hemochromatosis in 26 participants. Completed in 6 July 2017.

Timeline
24 October 2013
Primary endpoint
6 July 2017
6 July 2017

Quick facts

Lead sponsorRennes University Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment26
Start date24 October 2013
Primary completion6 July 2017
Estimated completion6 July 2017
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Rennes University Hospital

Who can join

18 and older, any sex, with Hemochromatosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Pharmacokinetics of tacrolimus are highly variable and may result in graft rejection (underdosing) or toxicity (overdosing). The risk of transplant rejection and the toxicity of tacrolimus can be reduced by pharmacological therapeutic monitoring of the molecule, based on the measurement of residual blood concentrations. Nevertheless, some patients are victims of rejections or toxic signs even though their blood concentrations are in the therapeutic target. The aim of the study is to describe the pharmacokinetics of tacrolimus diffusion in mononuclear cells as well as the kinetics of effect of the drug on its target protein

Publications & conference data

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

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Other recruiting trials for Hemochromatosis

Currently open trials in the same condition.

Other Rennes University Hospital trials

Trials by the same sponsor.

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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/NCT03654794.

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