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Efficacy and Safety of FTY720 in de Novo Adult Renal Transplant Recipients

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Novartis

Status and phase

Completed
Phase 2

Conditions

Renal Transplantation

Treatments

Drug: FTY720

Study type

Interventional

Funder types

Industry

Identifiers

NCT00239798
CFTY720A2218E1

Details and patient eligibility

About

This study will evaluate the safety and efficacy of FTY720 combined with cyclosporine and corticosteroids in patients receiving a kidney transplant.

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  • Patients who have completed the 12 Month visit of the Core trial either on or off study drug.
  • Female capable of becoming pregnant are required to have a medically approved method of birth control until 3 Month after study medication was stopped.

Exclusion Criteria

  • None

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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