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Drug-Drug Interaction Study Between EDP-938, Itraconazole, Rifampin, and Quinidine in Healthy Subjects

Primary Purpose

RSV Infection

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
EDP-938
EDP-938
EDP-938
Itraconazole
Rifampin
Quinidine
Sponsored by
Enanta Pharmaceuticals, Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for RSV Infection focused on measuring drug-drug interaction

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • An informed consent document signed and dated by the subject.
  • Healthy male and female subjects of any ethnic origin between the ages of 18 and 55 years, inclusive.
  • Screening body mass index (BMI) of 18 to 30 kg/m2 with a minimum body weight of 50 kg
  • Female subjects of childbearing potential must agree to use two effective methods of contraception from the date of Screening until 90 days after the last dose of EDP 938.

Exclusion Criteria:

  • Clinically relevant evidence or history of illness or disease.
  • For Part 3 subjects, the following cardiovascular abnormalities:

    • QRS duration >110 ms
    • Incomplete right bundle branch block or any complete bundle branch block
    • Heart rate <40 or >90 beats per minute (per vital sign capture while rested)
    • History of unexplained syncope, structural heart disease, or clinically significant arrhythmias
    • Personal or family history of long QT syndrome (genetically proven or suggested by sudden death of a close relative due to cardiac causes at a young age) or Brugada syndrome
    • PR interval >220 ms or any 2nd or 3rd degree AV block
    • Ventricular pre-excitation
  • Pregnant or nursing females.
  • History of febrile illness within 7 days prior to the first dose of study drug or subjects with evidence of active infection.
  • A positive urine drug screen at Screening or Day -1.
  • Current tobacco smokers or use of tobacco within 3 months prior to Screening.
  • Any condition possibly affecting drug absorption (e.g., gastrectomy, cholecystectomy).
  • History of regular alcohol consumption.
  • Participation in a clinical trial within 30 days prior to the first dose of study drug.

Sites / Locations

  • Pharmaceutical Research Associates, Inc.,

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

EDP-938 and itraconazole interaction (Part 1)

EDP-938 and rifampin interaction (Part 2)

EDP-938 and quinidine interaction (Part 3)

Arm Description

Outcomes

Primary Outcome Measures

Cmax of EDP-938 with and without coadministration with itraconazole
AUC of EDP-938 with and without coadministration with itraconazole
Cmax of EDP-938 with and without coadministration with rifampin
AUC of EDP-938 with and without coadministration with rifampin
Cmax of EDP-938 with and without coadministration with quinidine
AUC of EDP-938 with and without coadministration with quinidine

Secondary Outcome Measures

Safety measured by adverse events

Full Information

First Posted
November 26, 2018
Last Updated
June 12, 2019
Sponsor
Enanta Pharmaceuticals, Inc
Collaborators
Pharmaceutical Research Associates
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1. Study Identification

Unique Protocol Identification Number
NCT03755778
Brief Title
Drug-Drug Interaction Study Between EDP-938, Itraconazole, Rifampin, and Quinidine in Healthy Subjects
Official Title
A Non-Randomized, Open-Label, Three-Part, Drug-Drug Interaction Study to Evaluate the Effects of Itraconazole, Rifampin, and Quinidine on the Pharmacokinetics and Safety of EDP-938 in Healthy Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
November 29, 2018 (Actual)
Primary Completion Date
January 21, 2019 (Actual)
Study Completion Date
January 27, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Enanta Pharmaceuticals, Inc
Collaborators
Pharmaceutical Research Associates

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A Non-Randomized, Open-Label, Three-Part, Drug-Drug Interaction Study to Evaluate the Effects of Itraconazole, Rifampin, and Quinidine on the Pharmacokinetics and Safety of EDP-938 in Healthy Subjects

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
RSV Infection
Keywords
drug-drug interaction

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
3-Part Single Group study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EDP-938 and itraconazole interaction (Part 1)
Arm Type
Experimental
Arm Title
EDP-938 and rifampin interaction (Part 2)
Arm Type
Experimental
Arm Title
EDP-938 and quinidine interaction (Part 3)
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Day 1 and 14 (Part 1)
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Day 1 and 14 (Part 2)
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Day 1 and 8 (Part 3)
Intervention Type
Drug
Intervention Name(s)
Itraconazole
Intervention Description
Subjects will receive itraconazole once daily from Day 5 to Day 18
Intervention Type
Drug
Intervention Name(s)
Rifampin
Intervention Description
Subjects will receive rifampin once daily from Day 5 to Day 16
Intervention Type
Drug
Intervention Name(s)
Quinidine
Intervention Description
Subjects will receive quinidine once daily from Day 5 to Day 12
Primary Outcome Measure Information:
Title
Cmax of EDP-938 with and without coadministration with itraconazole
Time Frame
Up to 19 days
Title
AUC of EDP-938 with and without coadministration with itraconazole
Time Frame
Up to 19 days
Title
Cmax of EDP-938 with and without coadministration with rifampin
Time Frame
Up to 17 days
Title
AUC of EDP-938 with and without coadministration with rifampin
Time Frame
Up to 17 days
Title
Cmax of EDP-938 with and without coadministration with quinidine
Time Frame
Up to 13 days
Title
AUC of EDP-938 with and without coadministration with quinidine
Time Frame
Up to 13 days
Secondary Outcome Measure Information:
Title
Safety measured by adverse events
Time Frame
Up to 25 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: An informed consent document signed and dated by the subject. Healthy male and female subjects of any ethnic origin between the ages of 18 and 55 years, inclusive. Screening body mass index (BMI) of 18 to 30 kg/m2 with a minimum body weight of 50 kg Female subjects of childbearing potential must agree to use two effective methods of contraception from the date of Screening until 90 days after the last dose of EDP 938. Exclusion Criteria: Clinically relevant evidence or history of illness or disease. For Part 3 subjects, the following cardiovascular abnormalities: QRS duration >110 ms Incomplete right bundle branch block or any complete bundle branch block Heart rate <40 or >90 beats per minute (per vital sign capture while rested) History of unexplained syncope, structural heart disease, or clinically significant arrhythmias Personal or family history of long QT syndrome (genetically proven or suggested by sudden death of a close relative due to cardiac causes at a young age) or Brugada syndrome PR interval >220 ms or any 2nd or 3rd degree AV block Ventricular pre-excitation Pregnant or nursing females. History of febrile illness within 7 days prior to the first dose of study drug or subjects with evidence of active infection. A positive urine drug screen at Screening or Day -1. Current tobacco smokers or use of tobacco within 3 months prior to Screening. Any condition possibly affecting drug absorption (e.g., gastrectomy, cholecystectomy). History of regular alcohol consumption. Participation in a clinical trial within 30 days prior to the first dose of study drug.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enanta Pharmaceuticals
Organizational Affiliation
Enanta Pharmaceuticals, Inc
Official's Role
Study Director
Facility Information:
Facility Name
Pharmaceutical Research Associates, Inc.,
City
Lenexa
State/Province
Kansas
ZIP/Postal Code
66219
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Drug-Drug Interaction Study Between EDP-938, Itraconazole, Rifampin, and Quinidine in Healthy Subjects

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