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NCT00863746 · ClinicalTrials.gov registry record · Phase 3

A 3rd/4th Line Placebo-controlled Trial of Sorafenib in Patients With Predominantly Non Squamous Non-Small Cell Lung Cancer (NSCLC).

A Phase 3 study, sponsored by Bayer.

Completed
Registry status
Phase 3
Development phase
703
Enrollment target

NCT00863746: Completed Phase 3 study, sponsored by Bayer.

NCT00863746 is a Phase 3 study that has completed, run by Bayer. The registered enrollment target is 703 participants, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00863746, a Phase 3 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 3
Development phase
703 participants
Enrollment target

Study Summary

The purpose of the study is to see if sorafenib plus best supportive care (i.e. in addition to the non-cancer treatments patients would normally receive) is an effective treatment for lung cancer compared to best supportive care alone. The safety and tolerability of the two treatment groups will also be compared. The goal of the study is to test the ability of sorafenib to improve survival compared to best supportive care alone.

Primary Outcome

Overall survival (OS) was defined as the time from date of randomization to date of death due to any cause. Overall survival of subjects alive at the time of analysis will be censored at their last date of follow-up or database cut off date whichever came first.

Interventions

  • DRUG Placebo
  • DRUG Sorafenib (Nexavar, BAY43-9006)

Trial Details

FieldValue
Enrollment Target 703 participants
Start Date 2009-04
Est. Completion 2013-04
Phase Phase 3
Bayer

591 total trials

What the finished NCT00863746 record still lists

NCT00863746 is an interventional study that assigns participants to a tested intervention. The registered 703 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00863746 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00863746 about?

NCT00863746 is a clinical study titled "A 3rd/4th Line Placebo-controlled Trial of Sorafenib in Patients With Predominantly Non Squamous Non-Small Cell Lung Cancer (NSCLC).". The purpose of the study is to see if sorafenib plus best supportive care (i.e. in addition to the non-cancer treatments patients would normally receive) is an effective treatment for lung cancer compared to best supportive care alone. The safety and tolerability of the two treatment groups will als...

What is the current status of trial NCT00863746?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 703 participants. The study started on 2009-04. Estimated completion is 2013-04.

What interventions are being tested in trial NCT00863746?

The interventions under investigation include: Placebo (DRUG), Sorafenib (Nexavar, BAY43-9006) (DRUG).

Who is sponsoring clinical trial NCT00863746?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00863746's enrollment target sits among peer trials

703 506th of 2000 higher than 1,495 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00863746, the US trial registry maintained by the National Library of Medicine. NCT00863746 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.