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Evaluation of (R)-Roscovitine Safety and Effects in Subjects With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation (ROSCO-CF)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02649751
Recruitment Status : Terminated (The centers have no longer patients. In September 2018, set up of a competitive international study.)
First Posted : January 7, 2016
Last Update Posted : December 13, 2018
Sponsor:
Collaborators:
ManRos Therapeutics
Cyclacel Pharmaceuticals, Inc.
Information provided by (Responsible Party):
University Hospital, Brest

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Terminated
Actual Primary Completion Date : July 26, 2018
Actual Study Completion Date : July 26, 2018