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OpenTrials
Completed

NCT Number: NCT03755778

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

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

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Pharmaceutical Research Associates, Inc.,

Lenexa, Kansas, 66219, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

EDP-938

Drug

Subjects will receive EDP-938 once daily on Day 1 and 14 (Part 1)

Itraconazole

Drug

Subjects will receive itraconazole once daily from Day 5 to Day 18

Rifampin

Drug

Subjects will receive rifampin once daily from Day 5 to Day 16

Quinidine

Drug

Subjects will receive quinidine once daily from Day 5 to Day 12

Primary outcomes

  1. Cmax of EDP-938 with and without coadministration with itraconazole

    Time frame: Up to 19 days

  2. AUC of EDP-938 with and without coadministration with itraconazole

    Time frame: Up to 19 days

  3. Cmax of EDP-938 with and without coadministration with rifampin

    Time frame: Up to 17 days

  4. AUC of EDP-938 with and without coadministration with rifampin

    Time frame: Up to 17 days

  5. Cmax of EDP-938 with and without coadministration with quinidine

    Time frame: Up to 13 days

  6. AUC of EDP-938 with and without coadministration with quinidine

    Time frame: Up to 13 days

Secondary outcomes

  1. Safety measured by adverse events

    Time frame: Up to 25 days

Sponsors and collaborators

Lead sponsor

Enanta Pharmaceuticals, Inc

Industry

Collaborators

  • Pharmaceutical Research Associates

Registry information

Official study 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

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Nov 28, 2018
Registry last updated
Jun 14, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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