Ignite Creation Date:
2024-05-06 @ 10:31 AM
Last Modification Date:
2024-10-26 @ 12:31 PM
Study NCT ID:
NCT03277066
Status:
COMPLETED
Last Update Posted:
2021-12-23
First Post:
2017-09-06
Brief Title:
A 4-week Study to Evaluate the Efficacy and Safety of HP-5000 in Subjects With Knee Osteoarthritis
Sponsor:
Noven Pharmaceuticals Inc
Organization:
Noven Therapeutics
Study Overview
Official Title:
A 4-week Randomized Double-blind Multicenter Placebo-controlled Phase 2 Study to Evaluate the Efficacy and Safety of HP-5000 in Subjects With Osteoarthritis OA of the Knee
Status:
COMPLETED
Status Verified Date:
2021-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
HP-5000
Brief Summary:
A 4-week Randomized Double-blind Multicenter Placebo-controlled Phase 2 Study to Evaluate the Efficacy and Safety of HP-5000 in Subjects with Osteoarthritis OA of the Knee
Detailed Description:
This is a multicenter randomized double-blind and placebo-controlled phase 2 study evaluating 2 formulations of HP-5000 in subjects with OA of the knee The study will consist of up to 28-day Screening Phase that will include a Washout Period of current prescription and over the counter OTC analgesics a 4-week double-blind Treatment Phase and a 1-week safety Follow-up Period
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None