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NCT01708889 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetic Study of BMS-914143 in Participants With Normal Renal Function and Mild, Moderate, Severe and End-stage Renal Dysfunction

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

Completed
Registry status
Phase 1
Development phase
43
Enrollment target

NCT01708889: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT01708889 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 43 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01708889, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this study is to determine the effect of renal impairment on pharmacokinetics (PK) of BMS-914143.

Interventions

  • BIOLOGICAL BMS-914143 (Peginterferon Lambda-1a)

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2012-09
Est. Completion 2013-02
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT01708889 record still lists

NCT01708889 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 1 intervention - of which BMS-914143 (Peginterferon Lambda-1a) is the first listed.

NCT01708889 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01708889 about?

NCT01708889 is a clinical study titled "Pharmacokinetic Study of BMS-914143 in Participants With Normal Renal Function and Mild, Moderate, Severe and End-stage Renal Dysfunction". The purpose of this study is to determine the effect of renal impairment on pharmacokinetics (PK) of BMS-914143.

What is the current status of trial NCT01708889?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 2012-09. Estimated completion is 2013-02.

What interventions are being tested in trial NCT01708889?

The interventions under investigation include: BMS-914143 (Peginterferon Lambda-1a) (BIOLOGICAL).

Who is sponsoring clinical trial NCT01708889?

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 NCT01708889's enrollment target sits among peer trials

43 1100th of 2000 higher than 896 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

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Source: ClinicalTrials.gov NCT01708889, the US trial registry maintained by the National Library of Medicine. NCT01708889 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.