This open-label, inpatient pilot study is to assess the safety of lofexidine (1.6 2.4, and 4.0 mg per day) in the treatment of opiate-dependent individuals under-going medically-supervised opiate withdrawal. A secondary goal of the study is to provide preliminary evidence for the potential of lofexidine 2.4 mg per day, to reduce both the signs and symptoms opiate withdrawal. The results of this study will be used to determine the dose of lofexidine to be employed in a sub-sequent placebo-controlled, double-blind investigation using an analogous set of dependent measures.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000865-26S1
Application #
6118440
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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