Clinical Trials · NCT02217839

Multiple Ascending Dose Tolerability, Pharmacokinetic and Pharmacodynamic Study of DG3173

CompletedPhase 1Octreotide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Aspireo Pharmaceuticals Limited
Enrollment
42
Start date
Apr 2012
Locations
See registry
Primary endpoint
Number of serious adverse events or withdrawals due to adverse events. Laboratory investigations (including biochemistry, hematology, and urinalysis), vital signs (blood pressure, pulse rate), and 12-lead ECG.
View Octreotide compound reference