A Drug-drug Interaction Study Between Daclatasvir and Atazanavir/Ritonavir or Atazanavir/Cobicistat

• Status: Completed
• Trial end date: 2016-01-01
• Target enrollment: 0
• Participant gender: All

Summary

This study aims to provide the evidence that 150mg of cobicistat will have the same effect on the pharmacokinetics of daclatasvir 30mg QD as 100mg of ritonavir, when given together with atazanavir 300mg.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Radboud University
• Treatments: Anti-Retroviral Agents; Atazanavir Sulfate; Cobicistat; Ritonavir

Criteria

Inclusion Criteria:

1. Subject is at least 18 and not older than 55 years at screening.

2. Subject does not smoke more than 10 cigarettes, 2 cigars, or 2 pipes per day for at least 3 months prior to Day 1.

3. Subject has a Quetelet Index (Body Mass Index) of 18 to 30 kg/m2, extremes included.

4. Subject is able and willing to sign the Informed Consent Form prior to screening evaluations.

5. Subject is in good age-appropriate health condition as established by medical history, physical examination, and electrocardiography, results of biochemistry, hematology and urinalysis testing within 4 weeks prior to day 1. Results of biochemistry, hematology and urinalysis testing should be within the laboratory's reference ranges (see Appendix A). If laboratory results are not within the reference ranges, the subject is included on condition that the Investigator judges that the deviations are not clinically relevant. This should be clearly recorded.

6. Subject has a normal blood pressure and pulse rate, according to the Investigator's judgment.

Exclusion Criteria:

1. Creatinine clearance below 60mL/min.

2. Documented history of sensitivity/idiosyncrasy to medicinal products or excipients.

3. Positive HIV test.

4. Positive hepatitis B or C test.

5. Pregnant female (as confirmed by an hCG test performed less than 4 weeks before day 1) or breast-feeding female. Female subjects of childbearing potential without adequate contraception, e.g. hysterectomy, bilateral tubal ligation, (non-hormonal) intrauterine device, total abstinence, double barrier methods, or two years post-menopausal. They must agree to take precautions in order to prevent a pregnancy throughout the entire conduct of the study.

6. Therapy with any drug (for two weeks preceding Day 1), except for acetaminophen (max 2 gram/day).

7. Relevant history or presence of pulmonary disorders (especially COPD), cardiovascular disorders, neurological disorders (especially seizures and migraine), psychiatric disorders, gastro-intestinal disorders, renal and hepatic disorders (clinically relevant increased ALAT/ASAT or hyperbilirubinemia) hormonal disorders (especially diabetes mellitus), coagulation disorders.

8. Relevant history or current condition that might interfere with drug absorption, distribution, metabolism or excretion.

9. History of or current abuse of drugs, alcohol or solvents.

10. Inability to understand the nature and extent of the study and the procedures required.

11. Participation in a drug study within 60 days prior to Day 1.

12. Donation of blood within 60 days prior to Day 1.

13. Febrile illness within 3 days before Day 1.