A Phase 1, 2-Part, Single Ascending Dose Assessment of the Safety, Tolerability, and Pharmacokinetics of Rolapitant Intravenous in Healthy Volunteers

NCT ID: NCT02382666

Last Updated: 2015-08-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-01-31
• Study Completion Date: 2015-08-31

Brief Summary

The purpose of this study is to assess the safety and tolerability of single increasing doses of intravenously administered rolapitant in healthy male and female subjects.

Detailed Description

Part 1 of the study is designed to evaluate the safety and tolerability of a SAD, up to 6 cohorts,of rolapitant IV (2 mg/mL solution) administered as an IV infusion over 30 minutes.

In Part 2 of the study, the safety and tolerability of the highest safe and well-tolerated dose established in Part 1 will be evaluated in an expanded cohort. The highest safe and well-tolerated dose established in Part 1 will be ascertained by the following criteria: an upper limit of 90% confidence interval (CI) for Cmax. A minimum of 40 subjects will be enrolled in Part 2.

Conditions

Chemotherapy-induced Nausea and Vomiting

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Rolapitant Cohort 1

Investigational Product: Rolapitant Dose 1 administered IV as a 30-minute infusion Dosage Form: 2 mg/mL solution

Group Type: EXPERIMENTAL

Rolapitant

Intervention Type: DRUG

Rolapitant Cohort 2

Investigational Product: Rolapitant Dose 2 administered IV as a 30-minute infusion Dosage Form: 2 mg/mL solution

Group Type: EXPERIMENTAL

Rolapitant

Intervention Type: DRUG

Rolapitant Cohort 3

Investigational Product: Rolapitant Dose 3 administered IV as a 30-minute infusion Dosage Form: 2 mg/mL solution

Group Type: EXPERIMENTAL

Rolapitant

Intervention Type: DRUG

Rolapitant Cohort 4

Investigational Product: Rolapitant Dose 4 administered IV as a 30-minute infusion Dosage Form: 2 mg/mL solution

Group Type: EXPERIMENTAL

Rolapitant

Intervention Type: DRUG

Rolapitant Cohort 5

Investigational Product: Rolapitant Dose 5 administered IV as a 30-minute infusion Dosage Form: 2 mg/mL solution

Group Type: EXPERIMENTAL

Rolapitant

Intervention Type: DRUG

Rolapitant Cohort 6

Investigational Product: Rolapitant Dose 6 administered IV as a 30-minute infusion Dosage Form: 2 mg/mL solution

Group Type: EXPERIMENTAL

Rolapitant

Intervention Type: DRUG

Interventions

Rolapitant

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subject must be a healthy male or female aged 18 to 55 years at Screening
• A female subject must have a negative pregnancy test at Screening and on Day -1.
• A female subject of childbearing potential must agree to use an accepted method of birth control (excluding hormonal birth control methods) from Screening through 30 days after final study drug administration.
• Subject must have a body mass index (BMI) from 18.5 to 32.0 kg/m2 and a weight of

≥ 50 kg at Screening.

• Subject must be able to provide informed consent after risks and benefits have been explained. Subject must also be willing and able to comply with the protocol requirements.
• Subject must be in general good health as determined by the Investigator based on pre-study medical, medication, and surgical history; physical examination; and clinical laboratory tests.

Exclusion Criteria

• Subject must not have been dosed with test drug or blinded study drug in another investigational study within 30 days or 5 half-lives of the biologic activity of the test drug, whichever is longer, before the time of first study dose.
• Subject must not have a history of hypersensitivity to rolapitant IV or any of its excipients or who have completed a study visit as part of a previous rolapitant study within the 6 months prior to first study drug administration (Day
• Subject must not have poor venous access or consider venipuncture intolerable.
• Subject must not have a history of significant complications or anxiety associated with the IV administration of medications that, in the opinion of the Investigator, could make the subject unable to complete dosing requirements.
• Subject must not be pregnant or lactating.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Tesaro, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dennis Vargo, MD

Role: STUDY_DIRECTOR

Tesaro, Inc.

Locations

Parexel

Baltimore, Maryland, United States

Countries

United States

Other Identifiers

PR-11-5022-C

Identifier Type: -

Identifier Source: org_study_id