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NCT00887627 · ClinicalTrials.gov registry record · Phase 1

Study to Compare Conivaptan Pharmacokinetics in Subjects With Mild & Moderate Kidney Function Impairment to Subjects With Normal Kidney Function

A Phase 1 study, sponsored by Cumberland Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT00887627: Completed Phase 1 study, sponsored by Cumberland Pharmaceuticals.

NCT00887627 is a Phase 1 study that has completed, run by Cumberland Pharmaceuticals. The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00887627, a Phase 1 study, has completed, sponsored by Cumberland Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

A study to compare a conivaptan PK in subjects with mild or moderate kidney function impairment to subjects with normal kidney function after a 48-hour continuous infusion of conivaptan.

Interventions

  • DRUG conivaptan hydrochloride

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2009-04
Est. Completion 2010-07
Phase Phase 1
Cumberland Pharmaceuticals

43 total trials

What the finished NCT00887627 record still lists

NCT00887627 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

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

NCT00887627 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00887627 about?

NCT00887627 is a clinical study titled "Study to Compare Conivaptan Pharmacokinetics in Subjects With Mild & Moderate Kidney Function Impairment to Subjects With Normal Kidney Function". A study to compare a conivaptan PK in subjects with mild or moderate kidney function impairment to subjects with normal kidney function after a 48-hour continuous infusion of conivaptan.

What is the current status of trial NCT00887627?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2009-04. Estimated completion is 2010-07.

What interventions are being tested in trial NCT00887627?

The interventions under investigation include: conivaptan hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00887627?

This trial is sponsored by Cumberland Pharmaceuticals, which has 43 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00887627's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 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 NCT00887627, the US trial registry maintained by the National Library of Medicine. NCT00887627 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.