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NCT01009593 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellular Carcinoma (HCC)

A Phase 3 study, sponsored by Abbott.

Terminated
Registry status
Phase 3
Development phase
1,035
Enrollment target

NCT01009593: Clinical Trial Phase 3 study, sponsored by Abbott.

NCT01009593 is a Phase 3 study that was terminated before completion, run by Abbott. The registered enrollment target is 1,035 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (34% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01009593, a Phase 3 study, was terminated before completion, sponsored by Abbott.

TERMINATED
Registry status
Phase 3
Development phase
1,035 participants
Enrollment target

Study Summary

The primary objective of this study is to assess the overall survival (OS) of oral linifanib given as monotherapy once daily (QD) compared to sorafenib given twice daily (BID) per standard of care in subjects with advanced or metastatic HCC.

Interventions

  • DRUG Sorafenib
  • DRUG ABT-869

Trial Details

FieldValue
Enrollment Target 1,035 participants
Start Date 2010-01
Est. Completion 2012-07
Phase Phase 3
Abbott

181 total trials

Why NCT01009593 stopped before completion

NCT01009593 is an interventional study that assigns participants to a tested intervention. Its 1,035 participants enrollment target places it among the larger protocols in the corpus, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (34% higher).

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

NCT01009593 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01009593 about?

NCT01009593 is a clinical study titled "Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellular Carcinoma (HCC)". The primary objective of this study is to assess the overall survival (OS) of oral linifanib given as monotherapy once daily (QD) compared to sorafenib given twice daily (BID) per standard of care in subjects with advanced or metastatic HCC.

What is the current status of trial NCT01009593?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 1,035 participants. The study started on 2010-01. Estimated completion is 2012-07.

What interventions are being tested in trial NCT01009593?

The interventions under investigation include: Sorafenib (DRUG), ABT-869 (DRUG).

Who is sponsoring clinical trial NCT01009593?

This trial is sponsored by Abbott, which has 181 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01009593's enrollment target sits among peer trials

1,035 287th of 2000 higher than 1,713 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 NCT01009593, the US trial registry maintained by the National Library of Medicine. NCT01009593 (large enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.