A Randomized, Double-blind, Placebo-controlled, Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of Ascending, Subcutaneous, Single and Multiple Doses of SHP681 (GLP-2 Analog-Fc Fusion) in Healthy Adult Subjects
Latest Information Update: 03 Oct 2021
At a glance
- Drugs SHP 681 (Primary)
- Indications Short bowel syndrome
- Focus Adverse reactions; Pharmacodynamics
- Sponsors Shire; Takeda
Most Recent Events
- 14 Feb 2020 Status changed from recruiting to completed.
- 27 Nov 2019 Planned End Date changed from 31 Dec 2019 to 6 Jan 2020.
- 27 Nov 2019 Planned primary completion date changed from 31 Dec 2019 to 6 Jan 2020.