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NCT00771953 · ClinicalTrials.gov registry record · Phase 2

0822GCC: Phase 2 Study of Efficacy and Safety of Apricoxib/Placebo With Docetaxel or Pemetrexed in Non-Small Cell Lung Cancer

A Phase 2 study, sponsored by University of Maryland, Baltimore.

Completed
Registry status
Phase 2
Development phase
109
Enrollment target

NCT00771953 is a Phase 2 study that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 109 participants.

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The verdict

NCT00771953, a Phase 2 study, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
Phase 2
Development phase
109 participants
Enrollment target

Study Summary

The primary objective is to determine the anti-tumor activity of the combination of apricoxib + either docetaxel (AP/DC) or pemetrexed (AP/PE) compared with placebo + either docetaxel (P/DC) or pemetrexed (P/PE) as measured by progression free survival in patients with Stage IIIb (pleural effusion)or Stage IV non-small cell lung cancer (NSCLC).

Interventions

  • DRUG Placebo
  • DRUG apricoxib
  • DRUG Docetaxel or Pemetrexed

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2008-11
Est. Completion 2014-12
Phase Phase 2

Sponsor

University of Maryland, Baltimore

560 total trials

What the Registry Record Tells You About NCT00771953

The ClinicalTrials.gov registry entry for NCT00771953 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 109 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT00771953 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00771953 about?

NCT00771953 is a clinical study titled "0822GCC: Phase 2 Study of Efficacy and Safety of Apricoxib/Placebo With Docetaxel or Pemetrexed in Non-Small Cell Lung Cancer". The primary objective is to determine the anti-tumor activity of the combination of apricoxib + either docetaxel (AP/DC) or pemetrexed (AP/PE) compared with placebo + either docetaxel (P/DC) or pemetrexed (P/PE) as measured by progression free survival in patients with Stage IIIb (pleural effusion)o...

What is the current status of trial NCT00771953?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 109 participants. The study started on 2008-11. Estimated completion is 2014-12.

What interventions are being tested in trial NCT00771953?

The interventions under investigation include: Placebo (DRUG), apricoxib (DRUG), Docetaxel or Pemetrexed (DRUG).

Who is sponsoring clinical trial NCT00771953?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

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

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.