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NCT00108953 · ClinicalTrials.gov registry record · Phase 2

A Research Study to Treat Patients With Advanced Hepatocellular Carcinoma

A Phase 2 study, sponsored by Bayer.

Completed
Registry status
Phase 2
Development phase
96
Enrollment target

NCT00108953: Completed Phase 2 study, sponsored by Bayer.

NCT00108953 is a Phase 2 study that has completed, run by Bayer. The registered enrollment target is 96 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00108953, a Phase 2 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 2
Development phase
96 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and efficacy of doxorubicin plus sorafenib versus doxorubicin plus placebo in patients with advanced hepatocellular carcinoma (HCC).

Primary Outcome

TTP was defined as the time from randomization to radiological disease progression by independent assessment.

Interventions

  • DRUG Sorafenib (Nexavar, BAY43-9006) plus Doxorubicin
  • DRUG Doxorubicin/Placebo

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2005-04
Est. Completion 2008-04
Phase Phase 2
Bayer

591 total trials

What the finished NCT00108953 record still lists

NCT00108953 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 2 interventions - of which Sorafenib (Nexavar, BAY43-9006) plus Doxorubicin is the first listed.

NCT00108953 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00108953 about?

NCT00108953 is a clinical study titled "A Research Study to Treat Patients With Advanced Hepatocellular Carcinoma". The purpose of this study is to evaluate the safety and efficacy of doxorubicin plus sorafenib versus doxorubicin plus placebo in patients with advanced hepatocellular carcinoma (HCC).

What is the current status of trial NCT00108953?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 96 participants. The study started on 2005-04. Estimated completion is 2008-04.

What interventions are being tested in trial NCT00108953?

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

Who is sponsoring clinical trial NCT00108953?

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

How this trial's enrollment target compares

Where NCT00108953's enrollment target sits among peer trials

96 747th of 2000 higher than 1,242 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00108953, the US trial registry maintained by the National Library of Medicine. NCT00108953 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.