Ignite Creation Date:
2024-05-05 @ 10:22 AM
Last Modification Date:
2024-10-26 @ 9:01 AM
Study NCT ID:
NCT00000302
Status:
COMPLETED
Last Update Posted:
2005-11-07
First Post:
1999-09-20
Brief Title:
Study Comparing Liquid and Tablet Buprenorphine Formulations - 5
Sponsor:
National Institute on Drug Abuse NIDA
Organization:
National Institute on Drug Abuse NIDA
Study Overview
Official Title:
Expanded Steady-State Pharmacokinetic Study Comparing Liquid and Tablet Buprenorphine Formulations
Status:
COMPLETED
Status Verified Date:
2002-12
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:
None
Brief Summary:
The purpose of this study is to compare liquid and tablet buprenorphine formulations
Detailed Description:
Participants were inducted on either liquid or tablet buprenorphine in a double-blind double-dummy manner They each reached a steady state by the second week and were scheduled to have blood draws in weeks 3 4 7 8 11 12 15 and 16
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| P50-09260-5 | None | None | None |