Overview

Phase 1 Study of Relative Bioavailability of PPI-668 New Tablet Versus Capsule Formulations

Status:
Completed
Trial end date:
2014-12-01
Target enrollment:
0
Participant gender:
All
Summary
This study will compare the blood levels of PPI-668 resulting from two different formulations - the current capsule and a new tablet, T003.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Presidio Pharmaceuticals, Inc.
Criteria
Inclusion Criteria:

- Have the ability to understand and sign a written informed consent form

- nonsmoker

- body mass index (BMI) of 18.0 to 29.9 kg/m2 (inclusive)

- HIV-1 antibody negative.

- hepatitis B (HBV) surface antigen negative.

- hepatitis C (HCV) antibody negative.

Exclusion Criteria:

- Pregnant or lactating subjects.

- Have any serious or active medical or psychiatric illness which, in the opinion of the
Investigator, would interfere with subject treatment, assessment, or compliance with
the protocol. This would include renal, cardiac, hematologic, hepatic, pulmonary
(including chronic asthma), endocrine (e.g., diabetes), central or peripheral nervous,
gastrointestinal (including an ulcer), vascular, metabolic (thyroid disorders, adrenal
disease), or immunodeficiency disorders, active infection, or malignancy that is
clinically significant or requiring treatment.

- Have participated in an investigational trial involving administration of any
investigational compound within 30 days prior to the study dosing.

- Current alcohol or substance abuse judged by the Investigator to potentially interfere
with subject compliance.

- Have poor venous access and unable to donate blood.

- Have donated blood within 56 days of study dosing.

- Have donated plasma within 7 days of study dosing.

- Have taken any prescription medications or over-the-counter medications including
herbal products within 28 days of commencing study drug dosing with the exception of
vitamins and/or acetaminophen and/or ibuprofen and/or contraceptive medications.