Phase 4
Completed N=5
Pharmacokinetics of Sublingual Versus Oral Tacrolimus in Patients Awaiting Kidney Transplantation
Kidney Failure, Chronic
Source: ClinicalTrials.gov NCT00629122 ↗
Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Dec 2017
Primary outcomePrimary: C0 (ng/mL) — 1.45; 6.2; 1.25; 6.5 ng/mL
◆ Published Evidence
No publication linked
No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.
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.
Outcome Measures
| Outcome | Result | p-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 |
— | — |
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)
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. Informational only — not medical advice.