Overview

A Study to Evaluate the Intramuscular Administration of Scopolamine

Status:
Recruiting
Trial end date:
2022-12-01
Target enrollment:
Participant gender:
Summary
To characterize the safety and tolerability profile of ascending doses of scopolamine hydrobromide trihydrate (Scopolamine HBT) administered by intramuscular (IM) injection. And characterize the pharmacokinetics (PK) of ascending doses of Scopolamine HBT administered by IM injection
Phase:
Phase 1
Details
Lead Sponsor:
U.S. Army Medical Research and Development Command
Treatments:
Butylscopolammonium Bromide
Scopolamine