This is a double-blind, randomized, placebo-controlled, multicenter clinical trial to evaluate the safety and efficacy of SP-303 for the treatment of AIDS associated diarrhea. The study design calls for the randomization of approximately 80 patients evaluable for efficacy in each of 4 treatment arms. After an initial inpatient treatment phase, responders will remain on their assigned treatment for an outpatient treatment phase (except patients treated with 500 mg delayed release beads who will be switched to 500 mg delayed release tablets for the outpatient treatment phase). Non-responders will be discontinued from treatment and discharged from the study. All patients will be evaluated for both safety and efficacy in an intent-to-treat analysis.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000750-27S3
Application #
6265129
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
27
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Type
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
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