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Clinical Trials/NCT01471704
NCT01471704
Completed
Phase 1

A Phase 1b, Drug-Drug Interaction Study Investigating the Pharmacokinetic Interaction Between INX-08189 and Verapamil HCL ER in Healthy Volunteers

Bristol-Myers Squibb1 site in 1 country24 target enrollmentOctober 2011

Overview

Phase
Phase 1
Intervention
INX-08189 50 mg
Conditions
Healthy
Sponsor
Bristol-Myers Squibb
Enrollment
24
Locations
1
Primary Endpoint
Safety of a single dose of INX-08189 50 mg alone & combined with verapamil HCL ER 240 mg after subjects received verapamil HCL ER QD for 6 days
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the potential for a pharmacokinetic (PK) drug-drug interaction between INX-08189 and extended release verapamil hydrochloride (verapamil HCL ER).

Detailed Description

This is a single-center, open-label, single-sequence, crossover, drug-drug interaction study in healthy subjects. Primary Objectives: Safety - To evaluate the safety of a single dose of INX-08189 (50 mg) alone and combined with verapamil HCL ER (240 mg) after subjects receive verapamil HCL ER QD for 6 days Pharmacokinetic - To evaluate the effect of multiple doses of verapamil HCL ER (240 mg) on the pharmacokinetic (PK) profile of INX-08189 and the metabolite INX-08032, and the effect of a single dose of INX-08189 on the PK profile of verapamil and the metabolite norverapamil

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
November 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects must meet the following criteria at the screening visit (Visit1) and Visit 2 in order to be eligible for study drug administration:
  • Must be a healthy male or female between 18 and 55 years of age (inclusive) with body mass index (BMI) between 18 and 30 kg/m2 (inclusive), and weigh \> 50 kg at the time of signing the informed consent;
  • Capable of giving written informed consent that includes compliance with the requirements and restrictions listed in the consent form. Signed informed consent must be on file prior to screening procedures;
  • Subject is able to understand and comply with the protocol requirements, instructions and restrictions;
  • Must be a non-tobacco user for at least 3 months prior to selection;
  • Healthy on the basis of physical examination, medical history, vital signs, electrocardiogram and clinical laboratory tests at screening;
  • Women must be postmenopausal for at least 2 years or be surgically sterile with complete hysterectomy or bilateral oophorectomy, and not be pregnant nor be breastfeeding;
  • Male subjects, who are not surgically sterile with vasectomy, must agree to use a double barrier method of birth control, such as, a condom plus spermicidal agent (foam/gel/film/cream/suppository). This criterion must be followed from the time of the first dose of study medication until 30 days after the last dose of medication. Male subjects cannot donate sperm during the study and for 3 months after receiving the last dose of the study drug.

Exclusion Criteria

  • Subjects must NOT meet the following criteria at the Screening Visit (Visit1), in order to be eligible for study drug administration at Visit 2:
  • Infection with Hepatitis A, B or C Virus;
  • Infection with the Human Immunodeficiency Virus (HIV);
  • History of or any current medical condition which could impact the safety of the participant in the study;
  • Current active or underlying GI, cardiovascular, neurologic, psychiatric, metabolic, renal, hepatic, respiratory, inflammatory, or infectious disease;
  • Clinically significant abnormalities on centrally read ECG including evidence of bradycardia (rate \< 60 bpm) or evidence of PR prolongation;
  • Screening vital signs representing a heart rate of \< 60 bpm, systolic blood pressure \< 90 mm Hg, and diastolic blood pressure \< 60 mm Hg;
  • Currently significant diarrhea, gastric stasis, or constipation that in the investigator's opinion could influence drug absorption or bioavailability;
  • Safety laboratory abnormalities at screening which are clinically significant, or absolute neutrophil count of \< 1800 cells/mm3, or platelet count \< 130,000 cells/mm3, or hemoglobin \< 12 g/dl for women and \< 13 g/dl for men;
  • Women of child bearing potential, pregnant or breastfeeding;

Arms & Interventions

INX-08189 50 mg

Study Day 0: Single 50 mg dose of INX-08189 in the morning

Intervention: INX-08189 50 mg

240 mg verapamil HCL ER

Study Days 6 to 11: 240 mg verapamil HCL ER once daily (QD) in the morning

Intervention: 240 mg verapamil HCL ER

INX-08189 50 mg & verapamil HCLER 240 mg

Study Day 12: Co-administration of single 50 mg dose of INX-08189 and 240 mg verapamil HCL ER in the morning

Intervention: 50 mg dose of INX-08189 and 240 mg verapamil HCL ER

Outcomes

Primary Outcomes

Safety of a single dose of INX-08189 50 mg alone & combined with verapamil HCL ER 240 mg after subjects received verapamil HCL ER QD for 6 days

Time Frame: Study Day -1, during the 24-hours post-dose, Study Day 2 to 4, 5, 6, 7 to 11, 12, and 13 to 16

Safety and tolerability parameters, including adverse event, concurrent medication, clinical laboratory, electrocardiogram (ECG) and vital signs assessments

Effect of multiple doses of verapamil HCL ER 240 mg on the PK profile of INX-08189, and the effect of a single dose of INX-08189 on the PK profile of verapamil.

Time Frame: INX-08189 and Verapamil: Study Day 0 (INX-08189), Study Day 12 (Verapamil) and subsequently at 30 minutes, and 1, 1.5, 2, 3, 4, 5, 6, 8, 12, 24 hours after dosing. INX-08189 also at 48, 72, and 96 hours after initial dose.

PK for INX-08189 and verapamil by: maximum plasma concentration (Cmax), time Cmax is observed (Tmax), plasma concentration at end of dosing (Ctau), area under plasma concentration-time curve; time 0 to last measurable plasma concentration (AUC0-last), area under plasma concentration-time curve; time 0 to infinity (AUC0-inf), area under plasma concentration-time curve; 0 to end of dosing (AUC0-tau), elimination half-life (t1/2), apparent oral clearance (CL/F), and apparent oral volume of distribution (Vz/F).

Study Sites (1)

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