Viewing Study NCT01259102


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Study NCT ID: NCT01259102
Status: COMPLETED
Last Update Posted: 2012-09-03
First Post: 2010-12-10
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Examine Plasma Concentrations of Buprenorphine Following Reapplication of Buprenorphine Transdermal System (BTDS) After Variable Application Site Rest Periods
Sponsor: Purdue Pharma LP
Organization:

Organization Data

Organization:
Class: INDUSTRY
Study ID: BUP1002
Study Type: None
Study Domain: None
Study Link: None
Lead Sponsor:
Lead Sponsor Class: INDUSTRY
Responsible Party:
Responsible Party Title:
Responsible Party Type: SPONSOR
Responsible Party Affiliation:
Old Name: None
Old Organization: None

Collaborators