Drug-Drug Interaction Study Between EDP-938, Tacrolimus, Dabigatran, Rosuvastatin and Midazolam 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
Tacrolimus
Dabigatran
Rosuvastatin
EDP-938
Midazolam
Sponsored by
About this trial
This is an interventional basic science trial for RSV Infection focused on measuring drug-drug interaction
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
- 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.
- For Part 1 subjects:
- Clinical history or evidence at Screening consistent with hyperkalemia, hypertension and/or diabetes mellitus
- For Part 2 Subjects:
- Clinical history or evidence at screening of medically significant bleeding
- History of a mechanical heart valve placement, a thromboembolic event or clinically significant thrombotic event, an autoimmune disease, eg, systemic lupus erythematosus (SLE), or recurrent spontaneous abortions
- A platelet count <LLN, or INR >ULN, or aPTT > ULN at Screening
- Ongoing daily use of nonsteroidal anti-inflammatory drugs
- For Part 3 subjects:
- AST and/or ALT >ULN at Screening
- For Part 4 subjects:
- History of glaucoma
Sites / Locations
- Pharmaceutical Research Associates, Inc.,
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
EDP-938 and tacrolimus interaction (Part 1)
EDP-938 and dabigatran interaction (Part 2)
EDP-938 and rosuvastatin interaction (Part 3)
EDP-938 and midazolam interaction (Part 4)
Arm Description
Outcomes
Primary Outcome Measures
Cmax of tacrolimus with and without coadministration with EDP-938
AUC of tacrolimus with and without coadministration with EDP-938
Cmax of dabigatran with and without coadministration with EDP-938
AUC of dabigatran with and without coadministration with EDP-938
Cmax of rosuvastatin with and without coadministration with EDP-938
AUC of rosuvastatin with and without coadministration with EDP-938
Cmax of midazolam with and without coadministration with EDP-938
AUC of midazolam with and without coadministration with EDP-938
Secondary Outcome Measures
Safety measured by adverse events
Full Information
NCT ID
NCT04498741
First Posted
July 30, 2020
Last Updated
October 12, 2021
Sponsor
Enanta Pharmaceuticals, Inc
Collaborators
Pharmaceutical Research Associates
1. Study Identification
Unique Protocol Identification Number
NCT04498741
Brief Title
Drug-Drug Interaction Study Between EDP-938, Tacrolimus, Dabigatran, Rosuvastatin and Midazolam in Healthy Subjects
Official Title
A Non-Randomized, Open-Label, Three-Part, Drug-Drug Interaction Study to Evaluate the Effects of EDP-938 on the Pharmacokinetics of Tacrolimus, Dabigatran, Rosuvastatin and Midazolam in Healthy Subjects
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
July 8, 2020 (Actual)
Primary Completion Date
May 27, 2021 (Actual)
Study Completion Date
June 1, 2021 (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 tacrolimus, dabigatran, rosuvastatin and midazolam 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
4-Part Single Group study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
89 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EDP-938 and tacrolimus interaction (Part 1)
Arm Type
Experimental
Arm Title
EDP-938 and dabigatran interaction (Part 2)
Arm Type
Experimental
Arm Title
EDP-938 and rosuvastatin interaction (Part 3)
Arm Type
Experimental
Arm Title
EDP-938 and midazolam interaction (Part 4)
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Days 10 through 27 (Part 1)
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Days 5 through 15 (Part 2)
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Days 5 through 15 (Part 3)
Intervention Type
Drug
Intervention Name(s)
Tacrolimus
Intervention Description
Subjects will receive tacrolimus once daily on Day 1 and Day 24
Intervention Type
Drug
Intervention Name(s)
Dabigatran
Intervention Description
Subjects will receive dabigatran once daily on Day 1 and Day 13
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Intervention Description
Subjects will receive rosuvastatin once daily on Day 1 and Day 13
Intervention Type
Drug
Intervention Name(s)
EDP-938
Intervention Description
Subjects will receive EDP-938 once daily on Days 3 through 16 (Part 4)
Intervention Type
Drug
Intervention Name(s)
Midazolam
Intervention Description
Subjects will receive midazolam once daily on Day 1 and Day 16
Primary Outcome Measure Information:
Title
Cmax of tacrolimus with and without coadministration with EDP-938
Time Frame
up to 29 days
Title
AUC of tacrolimus with and without coadministration with EDP-938
Time Frame
up to 29 days
Title
Cmax of dabigatran with and without coadministration with EDP-938
Time Frame
up to 17 days
Title
AUC of dabigatran with and without coadministration with EDP-938
Time Frame
up to 17 days
Title
Cmax of rosuvastatin with and without coadministration with EDP-938
Time Frame
up to 17 days
Title
AUC of rosuvastatin with and without coadministration with EDP-938
Time Frame
up to 17 days
Title
Cmax of midazolam with and without coadministration with EDP-938
Time Frame
up to 17 days
Title
AUC of midazolam with and without coadministration with EDP-938
Time Frame
up to 17 days
Secondary Outcome Measure Information:
Title
Safety measured by adverse events
Time Frame
up to 34 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
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.
For Part 1 subjects:
Clinical history or evidence at Screening consistent with hyperkalemia, hypertension and/or diabetes mellitus
For Part 2 Subjects:
Clinical history or evidence at screening of medically significant bleeding
History of a mechanical heart valve placement, a thromboembolic event or clinically significant thrombotic event, an autoimmune disease, eg, systemic lupus erythematosus (SLE), or recurrent spontaneous abortions
A platelet count <LLN, or INR >ULN, or aPTT > ULN at Screening
Ongoing daily use of nonsteroidal anti-inflammatory drugs
For Part 3 subjects:
AST and/or ALT >ULN at Screening
For Part 4 subjects:
History of glaucoma
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enanta Pharmaceuticals, Inc
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
Plan to Share IPD
No
Learn more about this trial
Drug-Drug Interaction Study Between EDP-938, Tacrolimus, Dabigatran, Rosuvastatin and Midazolam in Healthy Subjects
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