trial
as of 2026-07-01Safety, Tolerability, Pharmacokinetics and Efficacy of 180 mg Subcutaneous Risperidone From 6 mg Oral Risperidone
NCTId NCT03978832
at a glance
Synthesized from structured facts only — each point cited above.
Design & status
Phase
Phase 4
Status
Completed
Enrollment
69 (actual)
Study type
Interventional
Allocation
Na
Model
Single Group
Masking
None
Start
2019-06-28
Primary completion
2020-05-12
Eligibility
ALL · 18 Years · 65 Years
Interventions & indications
Drugs
Indications
Sponsors
Indivior Inc.Lead Sponsor
Investigators
1
David P Walling, PhDPrincipal Investigator
Sites
1 total
Garden Grove, United States
Facts & assertions
4 sourced
Enrollment
69
Phase
PHASE4
Primary Completion Date
2020-05-12
Status
COMPLETED
relationships
The graph out of here
drug
drug
lead_sponsor
company
indication
indication
indication
investigator
person