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

NCT01250366 · ClinicalTrials.gov registry record · Phase 1

Study of the Safety & PK of INX-08189 in Chronically-infected HCV, Treatment-naïve Subjects

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
70
Enrollment target

NCT01250366: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT01250366 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 70 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01250366, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
70 participants
Enrollment target

Study Summary

The purpose of this study is to determine the Safety and Pharmacokinetics of Multiple Ascending Oral Doses of INX-08189 in Chronically-infected Genotype 1 HCV, Treatment-naïve Subjects.

Interventions

  • DRUG INX-08189

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2010-10
Est. Completion 2011-06
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT01250366 record still lists

NCT01250366 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% higher).

The record links to 0 conditions, and to 1 intervention - of which INX-08189 is the first listed.

NCT01250366 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01250366 about?

NCT01250366 is a clinical study titled "Study of the Safety & PK of INX-08189 in Chronically-infected HCV, Treatment-naïve Subjects". The purpose of this study is to determine the Safety and Pharmacokinetics of Multiple Ascending Oral Doses of INX-08189 in Chronically-infected Genotype 1 HCV, Treatment-naïve Subjects.

What is the current status of trial NCT01250366?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 70 participants. The study started on 2010-10. Estimated completion is 2011-06.

What interventions are being tested in trial NCT01250366?

The interventions under investigation include: INX-08189 (DRUG).

Who is sponsoring clinical trial NCT01250366?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01250366's enrollment target sits among peer trials

70 749th of 2000 higher than 1,227 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

  • NCT00969111 · 70 participants · NA

    Postoperative or Salvage Radiotherapy (RT) for Node Negative Prostate Cancer Following Radical Prostatectomy

  • NCT01712620 · 70 participants · Phase 2

    Spironolactone for Pulmonary Arterial Hypertension

  • NCT02143830 · 70 participants · Phase 2

    HSCT for Patients With Fanconi Anemia Using Risk-Adjusted Chemotherapy

  • NCT02601339 · 70 participants

    NIRS Monitoring in Premature Infants

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 NCT01250366, the US trial registry maintained by the National Library of Medicine. NCT01250366 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.