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Phase 4 N=5 Randomized Health Services Research

Pharmacokinetics of Sublingual Versus Oral Tacrolimus in Patients Awaiting Kidney Transplantation

Kidney Failure, Chronic

Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Dec 2017
Primary outcome: Primary: C0 (ng/mL) — 1.45; 6.2; 1.25; 6.5 ng/mL

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Tacrolimus (Arm B) (Drug); Clotrimazole Troche (Drug); Tacrolimus (Arm A) (Drug); Nystatin Suspension (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Weill Medical College of Cornell University
Primary completion
Dec 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
C0 (ng/mL)
1.45; 6.2; 1.25; 6.5
PRIMARY
Cmax
9.6; 14.0; 4.6; 19.5
PRIMARY
Tmax
1.75; 3.0; 0.875; 2.0
PRIMARY
Estimated AUC 0-6
9.3; NA; 4.9; NA; NA; 27.2
PRIMARY
Tacrolimus Powder Dissolution Time
2.25; 2.0
SECONDARY
Drug Interactions and Genotypes

Summary

Tacrolimus (Prograf) belongs to a class of medications known as the calcineurin inhibitors. It is a maintenance drug that is used to prevent rejection in kidney, liver, and heart transplant recipients. Calcineurin inhibitors display high pharmacokinetic (the body's effects on a drug) variability and necessitate use of blood tests to ensure that adequate drug levels are present to maintain effectiveness and safety. Early after transplant or at times when tacrolimus cannot be taken by mouth, alternative routes of administration are sought. Although an intravenous (through the vein) product is available, it can be toxic to the kidneys and has been associated with allergic reactions. Drug delivery via the oral mucosa is an alternative method of systemic drug administration which offers an alternative when oral administration is impractical (gastrointestinal dysmotility, reduced drug absorption, intestinal failure, difficulty in swallowing, or in those with nausea or vomiting). Administration of tacrolimus by the sublingual route may allow for direct entry into the systemic circulation and bypasses problems associated with drug absorption and breakdown that take place in the small intestine.

Eligibility Criteria

Inclusion Criteria

  • Adult patients awaiting kidney transplantation aged ≥ 18 years

Exclusion Criteria

  • Patients concurrently treated with medications that interact with tacrolimus (other than clotrimazole)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00629122). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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