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Once-a-day Regimen With Everolimus, Low Dose Cyclosporine and Steroids in Comparison With Steroid Withdrawal or Twice a Day Regimen With Everolimus, Low Dose Cyclosporine and Steroids.

Information source: Novartis
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: de Novo Kidney Transplant Recipients; Renal Transplantation

Intervention: everolimus (Drug); cyclosporine (Drug); Prednison (continuous steroids) (Drug)

Phase: Phase 3

Status: Completed

Sponsored by: Novartis

Official(s) and/or principal investigator(s):
Novartis Pharmaceuticals, Study Director, Affiliation: Novartis Pharmaceuticals

Summary

This study will compare the following immunosuppressive regimens in recipients of kidney transplantation: A) everolimus, cyclosporine and steroids given once-a-day; B) everolimus and cyclosporine given twice a day with steroid withdrawal; C) everolimus, cyclosporine given twice a day and continuous steroids. The purpose of this study is to evaluate regimens A and B in comparison with the control group (group C) for efficacy, using as main endpoint the treatment failure rate, a composite endpoint including death, graft loss, BPAR and lost to follow-up between randomization and Month 12.

Clinical Details

Official title: Once-a-day Regimen or Steroid Withdrawal in de Novo Kidney Transplant Recipients Treated With Everolimus, Cyclosporine and Steroids: a 12-month, Prospective, Randomized, Multicenter, Open-label Study. The EVIDENCE Study (EVerolImus Once-a-Day rEgimen With Neoral Versus Corticosteroid Elimination).

Study design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Primary outcome: Treatment Failure Rate

Secondary outcome:

Changes in the Estimated Glomerular Filtration Rate (eGFR) Between Randomization (Month 3) and Month 12

Biopsy Proven Acute Rejection (BPAR) Rate Between Randomization and Month 12

Number of Participants With Graft and Patient Survival After Randomization

Change in Estimated Creatine Clearance

Change in Serum Creatinine

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion criteria:

- recipients of 1st or 2nd single kidney transplant

- donor age >14 years

- females capable of becoming pregnant must have a negative serum pregnancy test within

7 days prior to or at Baseline (Visit 2), and are required to practice an approved method of birth control for the duration of the study and for a period of 2 months following discontinuation of study medication

- patientswho are willing and able to participate in the study and from whom written

informed consent has been obtained Exclusion criteria: Exclusion criteria at screening (pre-transplantation, Visit 1):

- recipients of kidney-pancreas transplant, double kidney or any other transplant

- recipients of a 2nd kidney transplant who lost the 1st for immunological reasons

- focal segmental glomerulosclerosis (FSGS), primary oxaluria or other diseases (as

cause of end stage renal failure - ESRF) at high risk of rapid recurrence or

requiring continuous corticosteroid treatment

- recipients of A-B-O incompatible transplants

- historical or current peak PRA of >25% (current = 3 months)

- patients with already existing antibodies against the donor

- thrombocytopenia (platelets <75,000/mm³), absolute neutrophil count of <1,500/mm³,

leucopenia (leucocytes <2,500/mm³), or hemoglobin <6 g/dL

- symptoms of significant somatic or mental illness. Inability to cooperate or

communicate with the investigator, or to comply with the study requirements, or to give informed consent

- history of malignancy of any organ system (other than localized basal cell carcinoma

of the skin), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases

- patients who are HIV positive or Hepatitis B surface antigen positive (HbsAg); HCV

positive patients receiving interferon and/or ribavirin

- evidence of severe liver disease (incl. abnormal liver enzyme profile, i. e. AST, ALT

or total bilirubin >3 times UNL)

- evidence of drug or alcohol abuse

- body mass index (BMI) >35

- patients who need to be treated with drugs known to strongly interact with CsA and/or

everolimus (as detailed in Appendix 2 of the protocol) should be excluded, if according the investigator this interferes with the objectives of the study

- women of child-bearing potential, UNLESS they are using two birth control methods.

The two methods can be a double barrier method or a barrier method plus a hormonal method

- pregnant or nursing (lactating) women, where pregnancy is defined as the state of a

female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test (>5 mIU/mL)

- use of other investigational drugs at the time of enrollment, or within 30 days or 5

half-lives of enrollment, whichever is longer

- history of hypersensitivity to any of the study drugs or to drugs of similar chemical

classes

- patients with severe active infections or any other medical condition(s) that in the

view of the investigator prohibits participation in the study (specify as required) Additional exclusion criteria post-transplantation (Visit 2): • graft not perfused or with thrombosis of the main vessels, according to angioscintigraphy or echocolordoppler within 48 hours after the end of surgical procedure To avoid any possible influence of the confounding factors on the results of this study additional exclusion criteria at randomization were (Visit 5, Month 3):

- unsatisfactory renal function (CrCl according Cockcroft and Gault<40 mL/min)

- proteinuria ≥0. 8 g/24 hrs

- steroid-resistant, humoral, moderate/severe (BANFF grade ≥II) biopsy proven acute

rejections

- multiple (2 or more) biopsy proven or treated acute rejections or acute rejections

leading to relevant loss of renal function

- acute rejection or impairment of renal function (increase of serum creatinine>30%) in

the month preceding randomization

- severe/uncontrollable adverse events with suspected relationship to everolimus (e. g.

anemia, oral aphtosis, arthralgia) for the control of which the investigator has planned the withdrawal of everolimus

- severe infections requiring hospitalization in the two weeks preceding randomization

- poor compliance to prescribed treatments

- Other protocol-defined inclusion/exclusion criteria may apply

Locations and Contacts

Novartis Investigative Site, Ancona 60100, Italy

Novartis Investigative Site, Bologna, Italy

Novartis Investigative Site, Brescia, Italy

Novartis Investigative Site, Cagliari, Italy

Novartis Investigative Site, Catania, Italy

Novartis Investigative Site, Coppito, Italy

Novartis Investigative Site, Firenze, Italy

Novartis Investigative Site, Genova 16132, Italy

Novartis Investigative Site, Milano 20122, Italy

Novartis Investigative Site, Modena 41100, Italy

Novartis Investigative Site, Napoli, Italy

Novartis Investigative Site, Novara 28100, Italy

Novartis Investigative Site, Padova, Italy

Novartis Investigative Site, Palermo, Italy

Novartis Investigative Site, Parma, Italy

Novartis Investigative Site, Perugia 06070, Italy

Novarits Investigative Site, Pisa, Italy

Novartis Investigative Site, Roma, Italy

Novartis Investigative Site, Rome, Italy

Novartis Investigative Site, Salerno, Italy

Novartis Investigative Site, Sassari 07100, Italy

Novartis Investigative Site, Siena 53100, Italy

Novartis Investigative Site, Torino 10126, Italy

Novartis Investigative Site, Treviso, Italy

Novartis InvestigativeSite, Udine, Italy

Novartis Investigative Site, Varese, Italy

Novartis Investigative Site, Verona, Italy

Novartis Investigative Site, Vicenza, Italy

Additional Information

Starting date: April 2009
Last updated: October 11, 2013

Page last updated: August 23, 2015

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