Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01472380 · ClinicalTrials.gov registry record · Phase 1

A Drug-Drug Interaction Study Between Fenofibric Acid and Efavirenz

A Phase 1 study, sponsored by Mutual Pharmaceutical Company.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT01472380: Completed Phase 1 study, sponsored by Mutual Pharmaceutical Company.

NCT01472380 is a Phase 1 study that has completed, run by Mutual Pharmaceutical Company. The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01472380, a Phase 1 study, has completed, sponsored by Mutual Pharmaceutical Company.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

Efavirenz is predominantly metabolized by cytochrome P450 (CYP) 2B6. Fenofibric Acid is an inhibitor of CYP2B6. This study will evaluate the effect of multiple doses of fenofibric acid at steady-state on the pharmacokinetics of single-dose efavirenz in healthy adult subjects.

Primary Outcome

The maximum or peak concentration that the drug reaches in the plasma for efavirenz

Interventions

  • DRUG efavirenz
  • DRUG fenofibric acid 105 mg

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2011-11
Est. Completion 2012-01
Phase Phase 1
Mutual Pharmaceutical Company

27 total trials

What the finished NCT01472380 record still lists

NCT01472380 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 2 interventions - of which efavirenz is the first listed.

NCT01472380 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01472380 about?

NCT01472380 is a clinical study titled "A Drug-Drug Interaction Study Between Fenofibric Acid and Efavirenz". Efavirenz is predominantly metabolized by cytochrome P450 (CYP) 2B6. Fenofibric Acid is an inhibitor of CYP2B6. This study will evaluate the effect of multiple doses of fenofibric acid at steady-state on the pharmacokinetics of single-dose efavirenz in healthy adult subjects.

What is the current status of trial NCT01472380?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2011-11. Estimated completion is 2012-01.

What interventions are being tested in trial NCT01472380?

The interventions under investigation include: efavirenz (DRUG), fenofibric acid 105 mg (DRUG).

Who is sponsoring clinical trial NCT01472380?

This trial is sponsored by Mutual Pharmaceutical Company, which has 27 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01472380's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01472380, the US trial registry maintained by the National Library of Medicine. NCT01472380 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.