Open Label Study Evaluating the Effects of a Single Oritavancin Infusion on Cytochrome P450 in Healthy Volunteers

NCT ID: NCT01784536

Last Updated: 2023-12-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-01-31
• Study Completion Date: 2013-03-31

Brief Summary

The purpose of this study is to examine the effects of oritavancin on the in vivo activities of CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP3A, NAT 2, and XO using a Cooperstown 5 + 1 cocktail in an open label, single arm manner.

Conditions

Healthy

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Oritavancin

Single-Dose IV Oritavancin Diphosphate

Group Type: EXPERIMENTAL

Single-Dose IV Oritavancin Diphosphate

Intervention Type: DRUG

Oritavancin will be administered as a single IV infusion. The infusion will last approximately 3 hours.

Interventions

Single-Dose IV Oritavancin Diphosphate

Oritavancin will be administered as a single IV infusion. The infusion will last approximately 3 hours.

Intervention Type: DRUG

Other Intervention Names

Oritavancin Diphosphate

Eligibility Criteria

Inclusion Criteria

• Provides written informed consent before study initiation.
• Healthy male or female adult between 18 and 45 years of age, inclusive.
• Body mass index (BMI) between 18 and 32 kg/m^2, inclusive.
• Nonsmoker for a 6-month period before Screening.
• In good health based upon results of medical history, physical examination, no clinically significant 12-lead ECG results, and laboratory test results.
• Agrees to avoid all medications (other than the study drugs) that may inhibit or induce hepatic microsomal enzymes during the study period, including prescription and nonprescription medications, vitamins, herbal supplements (including energy drinks), and nutraceuticals.
• Female subject is surgically sterile, postmenopausal, or, if of childbearing potential, agrees to use an acceptable nonhormonal method of contraception during all study phases.
• Agree to abstain from alcohol, caffeine-, and xanthine-containing products, all kind of energy drinks and the consumption of grapefruit juice and orange juice from 48 hours before study drug administration until completion of the follow-up visit.

Exclusion Criteria

• Has acute or chronic respiratory disease.
• The use of nonprescription drugs during the 30-day period before screening.
• The use of any prescription drugs during the 3-month period before.
• Childbearing potential, a positive test result for urine or serum, human chorionic gonadotropin (hCG) at Screening.
• Positive serology result for hepatitis B surface antigen, hepatitis C virus antibody, or has known hepatitis B or C infection at screening.
• Positive serology result for human immunodeficiency virus (HIV) or has known immune deficiency disease at Screening.
• Requires anticoagulant monitoring with an activated partial thromboplastin time.
• Has an elevated international normalized ratio >1.3.
• Surgical or medical condition that could interfere with the administration of the study drug.
• Any condition that may affect drug absorption.
• Has a known intolerance to benzodiazepines, the active and/or inactive ingredients in caffeine, warfarin, vitamin K, omeprazole, or dextromethorphan.
• The use of any nicotine containing substance or nicotine replacement devices within 6 months before Screening.
• Has received an immunization during the 2-week period before screening.
• Has hemorrhagic tendencies or blood dyscrasias.
• Has poor venous access as determined by the investigator.
• Reports regular alcohol intake exceeding 1 drink/day within 1 month before screening.
• A poor metabolizer (based on medical history, if known) of CYP2D6, CYP2C9, or CYP2C19.
• Has participated in other clinical research studies involving the evaluation of other investigational drugs or devices within 30 days before enrollment.
• Excluded for any of the previous criteria may not be rescreened for participation at any time.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Melinta Therapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Carlos Sanabria, MD

Role: PRINCIPAL_INVESTIGATOR

Spaulding Clinical

Locations

Spaulding Clinical

West Bend, Wisconsin, United States

Countries

United States

Other Identifiers

MDCO-ORI-12-03

Identifier Type: -

Identifier Source: org_study_id