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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03916380
Other study ID # 190617
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date May 31, 2019
Est. completion date June 30, 2020

Study information

Verified date April 2019
Source University of California, San Diego
Contact Shirley M Tsunoda, Pharm.D.
Phone 858-822-6629
Email smtsunoda@ucsd.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Transplant patients must take lifelong immunosuppression in order to prevent rejection of their organ. Tacrolimus is the most widely used immnosuppressive agent. Part of the routine education given to patients regarding tacrolimus is that they must avoid many drugs and substances that can interact with tacrolimus so that they don't experience side effects or lack of effect. Patients are told they must avoid readily available substances such as grapefruit juice and St. John's wort. A new once daily formulation of tacrolimus, Envarsus XR, may bypass the place in the gut in which many of these drug interactions occur. We will give kidney transplant patients Envarsus with and without grapefruit juice and measure the effect on blood levels throughout the day. Results from this study will also give us information about the likelihood of other drugs interacting with Envarsus XR.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date June 30, 2020
Est. primary completion date January 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Primary Kidney Transplant Age > 18 years At least 3 months post-transplantation Taking a stable dose of tacrolimus extended release with a target trough of 8-10 ng/mL BMI between 18-32

Exclusion Criteria:

- Multi-organ transplant Concomitant use of mTOR inhibitor Concomitant use of belatacept Concomitant use of medication affecting CYP3A or P-gp History of rejection Hypersensitivity to midazolam Hypersensitivity to Envarsus Active diarrhea or constipation BMI < 18 or > 32

Study Design


Intervention

Dietary Supplement:
Grapefruit Juice
Single 8 ounce administration of oral grapefruit juice

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shirley M. Tsunoda

Outcome

Type Measure Description Time frame Safety issue
Primary Tacrolimus AUC before and after Grapefruit Juice 2-4 weeks
Secondary Tacrolimus AUC compared to Midazolam AUC 2-4 weeks
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