A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple Ascending Doses of the ABT-333 Tablet

Completed · Phase 1 · Has a placebo group

Conditions studied: HCV Infection

In brief

The purpose of this study is to assess the safety, tolerability and pharmacokinetics of escalating multiple doses of the ABT-333 tablet formulation in healthy adult subjects.

Key facts

Study ID

NCT00909636

Run by

Abbott

People needed

24

Starts

2009-05-01

Last updated by the study team

2010-10-13

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• overall healthy subjects between the ages of 18 to 55 years old;
• if female, subject must be either postmenopausal for at least 2 years or surgically sterile;
• females must have negative results for pregnancy tests performed;
• if male, subject must be surgically sterile or practicing at least 1 of the following methods of birth control:
• partner(s) using IUD,
• partner(s) using oral, injected or implanted methods of hormonal contraceptives,
• subject and/or partner(s) using double-barrier method;
• Body Mass Index is 18 to 29, inclusive

You may not qualify if…

• history of significant sensitivity to any drug;
• positive test for HAV IgM, HBsAg, HCV Ab or HIV Ab;
• history of gastrointestinal issues or procedures;
• history of seizures, diabetes or cancer (except basal cell carcinoma);
• clinically significant cardiovascular, respiratory (except mild asthma), renal, gastrointestinal, hematologic, neurologic, thyroid, or any uncontrolled medical illness or psychiatric disorder;
• use of tobacco or nicotine-containing products with the 6-month period prior to study drug administration;
• donation or loss of 550 mL or more blood volume or receipt of a transfusion of any blood product within 8 weeks prior to study drug administration;
• clinically significant abnormal screening laboratory analyses and ECGs:
• ALT > ULN,
• AST > ULN,
• ECG with QTcF>450 msec in females and >430 msec in males,
• or ECG with 2nd or 3rd degree atrioventricular block;
• current enrollment in another clinical study;
• previous enrollment in this study;
• recent (6-month) history of drug/alcohol abuse that could preclude adherence to the protocol;
• pregnant or breastfeeding female;
• requirement for any OTC and/or prescription medication, vitamins and/or herbal supplements on a regular basis or use within the 2-week period prior to the first dose of study drug administration or within 10 half-lives of the respective medication;
• use of known inhibitors or inducers of cytochrome P450 3A or cytochrome P450 2C8 within 1 month prior to study drug administration;
• positive screen for drugs of abuse, alcohol, or cotinine;
• receipt of any drug by injection within 30 days prior to study drug administration;
• receipt of any investigational product within a time period equal to 10 half-lives of the product or a minimum of 6 weeks prior to study drug administration;
• consumption of alcohol within 48 hours prior to study drug administration;
• consumption of grapefruit, grapefruit products, star fruit, or star fruit products within the 72-hour period prior to study drug administration;
• consideration by the investigator, for any reason, that the subject is an unsuitable candidate to receive ABT-333;
• history of cardiac disease, including family history of long-QT syndrome or unexplained sudden death.

Where it is running

• Site Reference ID/Investigator# 20081 — Waukegan, Illinois, United States

Full record on ClinicalTrials.gov

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