NCT Number: NCT01928147
A Phase 1a/1b Study of PPI-383 in Healthy Adults and Hepatitis C Patients
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.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
Investigational site, Phoenix, Mauritius
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Part I volunteers (single and multiple dose) - key inclusion criteria
- Healthy males
- Age 18 to 55 years
- Body mass index (BMI)18 to 32 kg/m2
Part II patients- key inclusion criteria
- Males, or females of non-childbearing potential
- Age 18 to 65 years
- Chronic hepatitis C, and absence of other known liver disease
- Seropositive for HCV antibody (HCV Ab) or HCV RNA at least once previously
- Seropositive for HCV Ab at screening
- Serum HCV RNA > 5 log10 IU/mL at screening
- HCV gt-1
- Treatment-naïve for hepatitis C:
- BMI 18 to 35 kg/m2
- Otherwise in good health, without severe or clinically significant chronic or recurrent conditions requiring frequent medical intervention or continual pharmacologic management, except for anti-hypertensive use
- No medical or psychosocial conditions that would potentially interfere with the subject's ability to comply with the study assessments or visit schedule.
Part II patients - key exclusion criteria
- Seropositive for human immunodeficiency virus (HIV) antibody or hepatitis B virus (HBV) surface antigen (HBsAg)
- Signs or symptoms of decompensated liver disease
- Evidence of cirrhosis or hepatocellular carcinoma
- Diabetes Mellitus treated with insulin or hypoglycemic agents
- Asthma requiring hospital admission within the preceding 12 months
- History of alcohol abuse or illicit drug use which could interfere with a patient's compliance with the protocol requirements
- Any of the following laboratory values at screening
- Haemoglobin (Hgb) <11 g/dL in women or 12 g/dL in men
- White blood cell count <4,000/mm3
- Absolute neutrophil count (ANC) < 1800 per mm3
- Platelet count <100,000 per mm3
- Serum creatinine > upper limit of normal (ULN) at the central study laboratory
- Serum albumin <3.4 g/dL
- Total bilirubin >2.0 mg/dL
- Clinically significant abnormality in the electrocardiograms (ECGs) at screening
Treatment and study plan
Placebo
DrugPrimary outcomes
-
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
Secondary outcomes
-
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
Sponsors and collaborators
Lead sponsor
Presidio Pharmaceuticals, Inc.
Industry
Registry information
Official study title
A Phase Ia and Ib Dose-Ranging Study to Assess the Safety, Pharmacokinetics, and Antiviral Efficacy of PPI-383 in Healthy Adults and Hepatitis C Patients
Important dates
- Study start
- 2013
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- Aug 23, 2013
- Registry last updated
- Nov 26, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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