Clinical trial
A Once-weekly, Repeated Dose, Placebo Controlled, Double Blind, Randomised Cross-over Trial Investigating Safety, Efficacy and Pharmacodynamics of FE 203799 in Patients With Short Bowel Syndrome With Intestinal Failure Requiring Parenteral Support Followed by an Additional Treatment Period in an Open Label Regimen.
NCT03415594 is registered in ClinicalTrials.gov with GlyPharma Therapeutics as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Once-weekly, Repeated Dose, Placebo Controlled, Double Blind, Randomised Cross-over Trial Investigating Safety, Efficacy and Pharmacodynamics of FE 203799 in Patients With Short Bowel Syndrome With Intestinal Failure Requiring Parenteral Support Followed by an Additional Treatment Period in an Open Label Regimen.
- Lead sponsor
- GlyPharma Therapeutics
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- May 8, 2018
- Completion date
- November 21, 2019
- Enrollment
- 8 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.