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NCT00543075 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetic Study of Genasense in Subjects With Normal Renal Function, Mildly Impaired Renal Function, and Moderately Impaired Renal Function

A Phase 1 study, sponsored by Genta Incorporated.

Completed
Registry status
Phase 1
Development phase
23
Enrollment target

NCT00543075 is a Phase 1 study that has completed, run by Genta Incorporated. The registered enrollment target is 23 participants.

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The verdict

NCT00543075, a Phase 1 study, has completed, sponsored by Genta Incorporated.

COMPLETED
Registry status
Phase 1
Development phase
23 participants
Enrollment target

Study Summary

To characterize the pharmacokinetics of G3139 in subjects with normal, mildly impaired, and moderately impaired renal function who receive Genasense 3 mg/kg/day by continuous intravenous infusion for 2 days (48 hours).

Interventions

  • DRUG Genasense (oblimersen, G3139)

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2006-05
Est. Completion 2009-09
Phase Phase 1

Sponsor

Genta Incorporated

12 total trials

What the Registry Record Tells You About NCT00543075

The ClinicalTrials.gov registry entry for NCT00543075 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Genta Incorporated, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Genasense (oblimersen, G3139) is the first listed.

NCT00543075 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00543075 about?

NCT00543075 is a clinical study titled "Pharmacokinetic Study of Genasense in Subjects With Normal Renal Function, Mildly Impaired Renal Function, and Moderately Impaired Renal Function". To characterize the pharmacokinetics of G3139 in subjects with normal, mildly impaired, and moderately impaired renal function who receive Genasense 3 mg/kg/day by continuous intravenous infusion for 2 days (48 hours).

What is the current status of trial NCT00543075?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2006-05. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00543075?

The interventions under investigation include: Genasense (oblimersen, G3139) (DRUG).

Who is sponsoring clinical trial NCT00543075?

This trial is sponsored by Genta Incorporated, which has 12 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.