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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00991510
Other study ID # 116B8
Secondary ID 2009-010562-31
Status Terminated
Phase Phase 4
First received
Last updated
Start date August 2009
Est. completion date October 2010

Study information

Verified date October 2018
Source Teva Pharmaceutical Industries
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to further investigate how much of the drug substance "mycophenolate mofetil" can be found in the blood of patients with kidney or renal transplants when treated with Myfenax® or CellCept®. Additionally, the safety and side effects of the two products will be compared. All information already available on these products indicates that the safety profiles of the two products will be the same.


Recruitment information / eligibility

Status Terminated
Enrollment 43
Est. completion date October 2010
Est. primary completion date October 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Renal transplant recipients at least 12 months post-transplantation aged = 18 years.

- Maintenance treatment with mycophenolate mofetil (in combination with tacrolimus with or without corticosteroids).

- Stable dose of mycophenolate mofetil (= 500 mg twice daily) with no changes in immunosuppressive regimen for at least 6 weeks prior to the start of the study.

- Stable renal graft function for at least 3 months.

- Female patients must be either post-menopausal for = 1 year, be surgically sterilized or a negative pregnancy test will be required immediately prior to study entry and such patients must continue to use effective contraception.

- Willingness to undergo the study-related procedures.

- Ability to comprehend and willingness to sign informed consent form.

Exclusion Criteria:

- History of allergy to mycophenolate mofetil, mycophenolic acid or any of the ingredients.

- Multi-organ recipients (e.g., kidney and pancreas) or previous transplant with any organ other than kidney.

- Rejection within the past 6 months prior to the start of the study.

- Severe clinically relevant co-existing disease.

- History of cancer other than skin cancer that has been cured.

- History of serious clinically relevant digestive system disease during the last 12 months prior to start of the study.

- Known or suspected hereditary deficiency of hypoxanthine-guanine-phosphoribosyltransferase (e.g., Lesch-Nyhan syndrome, Kelley-Seegmiller syndrome).

- Known or suspected liver impairment.

- Clinically significant thrombocytopenia, anaemia, leukopenia, or neutropenia

- Clinically significant laboratory and/or physical changes during the last 2 months prior to the start of the study.

- Use of azathioprine, cholestyramine, sevelamer, or probenecid within 2 weeks prior to the first administration of study medication.

- Change in concomitant medication during the 6 weeks prior to start of the study.

- Use of any drug, prescribed or over-the-counter, (except stable concomitant medication) within 2 weeks prior to the first administration of study medication.

- Planned or expected requirement for the use of live attenuated vaccines during the study.

- Positive testing for HIV, Hepatitis B and C.

- Clinical symptoms or laboratory evidence of cytomegalovirus infection in the last 6 month.

- Pregnant or breast-feeding women.

- Women of childbearing potential unable or unwilling to practice effective contraceptive measures for the duration of the study and for 6 weeks after the end of the study.

- History of known or suspected alcohol or drug abuse.

- Any other condition of the patient that, in the opinion of the investigator may compromise evaluation of the study treatment or may jeopardize patient's compliance or adherence to protocol requirements.

- Previous enrollment in this study or participation in any other drug investigational trial within the past 6 weeks prior to enrollment.

Study Design


Related Conditions & MeSH terms

  • Stable Renal Transplant Recipients

Intervention

Drug:
mycophenolate mofetil (Myfenax)
Each participant received at least 500 mg orally, twice daily (morning and evening) during those study periods labeled as 'T' (test drug). Participants receive the dose equivalent to the pre-study dose (within the recommended therapeutic range) of mycophenolate mofetil.
mycophenolate mofetil (Cellcept)
Each participant received at least 500 mg orally, twice daily (morning and evening) during those study periods labeled as 'R' (reference drug). Participants receive the dose equivalent to the pre-study dose (within the recommended therapeutic range) of mycophenolate mofetil.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Teva Pharmaceutical Industries Parexel

References & Publications (2)

Sunder-Plassmann G et al.: Results of a Comparative Bioavailability Study of Myfenax (Teva) and CellCept (Roche) in Stable Kidney Transplant Recipients. American Transplant Congress 2011. Abstract Number: 250308

Sunder-Plassmann G, Reinke P, Rath T, Wiecek A, Nowicki M, Moore R, Lutz J, Gaggl M, Ferkl M. Comparative pharmacokinetic study of two mycophenolate mofetil formulations in stable kidney transplant recipients. Transpl Int. 2012 Jun;25(6):680-6. doi: 10.11 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Area Under the Plasma Concentration-time Curve (AUC(0-6h)) of Mycophenolate Mofetil Area under the plasma concentration-time curve during a dosage interval at steady state (calculated using the trapezoidal rule, from t = 0 to t = 6 hours). Day 14 and Day 28 (end of first two cross-over periods) before drug administration and at 30 min, 1 hour, 1.5, 2, 3, 4, 5, 6, 8, 10, and 12 hours after drug administration
Primary Area Under the Plasma Concentration-time Curve (AUC(0-tau)) of Mycophenolate Mofetil For participants with a 0-12h profile: Area under the plasma concentration-time curve during a dosage interval at steady state (calculated using the trapezoidal rule, from t = 0 to t = 12 hours). For participants with a 0-6h profile: AUC(0-tau) was calculated based on AUC(0-6h) using the extrapolation formula according to Fleming. Day 14 and Day 28 (end of first two cross-over periods) before drug administration and at 30 min, 1 hour, 1.5, 2, 3, 4, 5, 6, 8, 10, and 12 hours after drug administration
Primary Maximum Observed Plasma Concentration (Cmax) of Mycophenolate Mofetil Cmax was directly obtained from measured values of plasma concentrations. Day 14 and Day 28 (end of first two cross-over periods) before drug administration and at 30 min, 1 hour, 1.5, 2, 3, 4, 5, 6, 8, 10, and 12 hours after drug administration
Secondary Minimum Observed Plasma Concentration (Cmin) of Mycophenolate Mofetil Cmin was directly obtained from measured values of plasma concentrations. Day 14 and Day 28 (end of first two cross-over periods) before drug administration and at 30 min, 1 hour, 1.5, 2, 3, 4, 5, 6, 8, 10, and 12 hours after drug administration
Secondary Plasma Concentrations of Mycophenolate Mofetil in Pre-Administration Samples (Cpd) Cpd was directly obtained from measured values of plasma concentrations. Day 14 and Day 28 (end of first two cross-over periods) before drug administration
Secondary Degree of Fluctuation of the Concentration Levels of Mycophenolate Mofetil Over One Dosing Interval (PTF) PTF was calculated as: (Cmax-Cmin)/(AUCt/t)*100 Day 14 and Day 28 (end of first two cross-over periods) before drug administration
Secondary Time Corresponding to Occurrence of Cmax (Tmax) of Mycophenolate Mofetil Tmax was directly obtained from measured values. Day 14 and Day 28 (end of first two cross-over periods) before drug administration
Secondary Summary of Participants With Adverse Events Summary of adverse events across three study time periods. The on-treatment time frame spanned the time during which study drug was administered. Relation to study drug was assessed by the investigator.
The Adverse Event count includes serious and non-serious AEs. A serious AE (SAE) was any event that resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity or congenital anomaly/birth defect or was an important medical event could have jeopardized the patient's safety or required medical or surgical intervention to prevent one of the outcomes listed above.
Severity was measured on a three-point scale: mild, moderate, severe.
Day 1 up to Day 112