🇺🇸 FDA
Pipeline program

Bioequivalence study comparing two temazepam 20 mg tablet formulations after fasted administration; an open, randomized, single centre, single dose study with crossover design in healthy subjects

3137001

Phase 1 other active

Quick answer

Bioequivalence study comparing two temazepam 20 mg tablet formulations after fasted administration; an open, randomized, single centre, single dose study with crossover design in healthy subjects for short-term treatment of insomnia is a Phase 1 program (other) at Orion with 1 ClinicalTrials.gov record(s).

Program details

Company
Orion
Indication
short-term treatment of insomnia
Phase
Phase 1
Modality
other
Status
active

Clinical trials