A Phase 1 interventional study of PPI-383 and Placebo in Hepatitis C, Chronic, sponsored by Presidio Pharmaceuticals, Inc.. Completed at 6 sites in 2 countries. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-11-26.
Sponsored by Presidio Pharmaceuticals, Inc. · Phase 1, Interventional, and Treatment
PPI-383 is an antiviral agent (an inhibitor of the hepatitis C virus NS5B polymerase) that is being developed as a potential treatment for hepatitis C virus infection. This study is being done to assess the dose-related safety and tolerance of PPI-383 when given to healthy volunteers for up to 5 days (Part I of the study) and to hepatitis C patients for up to 3 days (Part II). In addition, the study will assess how much PPI-383 is absorbed into the bloodstream. In Part II, the dose-related effect of PPI-383 on the amount of hepatitis C virus in patients' bloodstream (serum HCV RNA levels) also will be assessed.
Part I volunteers (single and multiple dose) - key inclusion criteria
Part II patients- key inclusion criteria
Part II patients - key exclusion criteria
Any of the following laboratory values at screening
There will be up to 10 sequential single dose cohorts to assess the bioavailability of different doses and formulations; a food effect cohort will be included.
Drug: PPI-383 · Drug: Placebo
Upon completion of the single dose cohorts, an additional cohort will receive the highest well-tolerated dose from the single dose cohorts or placebo once daily for five days; up to additional cohorts may receive multiple doses of different formulations or different regimens
Drug: PPI-383 · Drug: Placebo
Upon completion of the single and multiple dose healthy volunteer cohorts, there will be 3, and potentially 4, sequential cohorts of HCV patients
Drug: PPI-383 · Drug: Placebo
Safety and tolerability, as measured by clinical adverse events and laboratory assessments
Time frame: Part I, up to day 12; and Part II, up to day 17
PPI-383 plasma levels
Time frame: Part I, up to day 12; and Part II, up to day 17
serum HCV RNA levels
Time frame: Part II, up to day 17
This study is completed, as verified in Nov 2015. You cannot join it, but the record below documents what was studied.
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Presidio Pharmaceuticals, Inc.