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NCT00699374 · ClinicalTrials.gov registry record · Phase 3

Study Of Sunitinib Malate Versus Sorafenib In Patients With Inoperable Liver Cancer

A Phase 3 study, sponsored by Pfizer.

Terminated
Registry status
Phase 3
Development phase
1,075
Enrollment target

NCT00699374: Clinical Trial Phase 3 study, sponsored by Pfizer.

NCT00699374 is a Phase 3 study that was terminated before completion, run by Pfizer. The registered enrollment target is 1,075 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (39% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00699374, a Phase 3 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 3
Development phase
1,075 participants
Enrollment target

Study Summary

The study will evaluate the efficacy and safety of sunitinib (Arm A), given at 37.5 mg orally once daily, compared to sorafenib (Arm B), given orally at 400 mg twice daily, in patients with inoperable liver cancer. A total number of 1200 patients will be enrolled, 600 on Arm A and 600 on Arm B. Study treatment may be adjusted based on patient tolerance. and will be given until disease progression, occurrence of unacceptable toxicity, or other withdrawal criteria are met. After discontinuation of study treatment, patients will be followed up in order to collect information on further antineoplastic therapy and survival.

Primary Outcome

Overall survival is the duration from randomization to death. For participants who are alive, overall survival was censored at the last contact.

Interventions

  • DRUG sorafenib
  • DRUG sunitinib malate

Trial Details

FieldValue
Enrollment Target 1,075 participants
Start Date 2008-07
Est. Completion 2011-12
Phase Phase 3
Pfizer

1,845 total trials

Why NCT00699374 stopped before completion

NCT00699374 is an interventional study that assigns participants to a tested intervention. Its 1,075 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 (39% higher).

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

NCT00699374 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00699374 about?

NCT00699374 is a clinical study titled "Study Of Sunitinib Malate Versus Sorafenib In Patients With Inoperable Liver Cancer". The study will evaluate the efficacy and safety of sunitinib (Arm A), given at 37.5 mg orally once daily, compared to sorafenib (Arm B), given orally at 400 mg twice daily, in patients with inoperable liver cancer. A total number of 1200 patients will be enrolled, 600 on Arm A and 600 on Arm B. Stud...

What is the current status of trial NCT00699374?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 1,075 participants. The study started on 2008-07. Estimated completion is 2011-12.

What interventions are being tested in trial NCT00699374?

The interventions under investigation include: sorafenib (DRUG), sunitinib malate (DRUG).

Who is sponsoring clinical trial NCT00699374?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00699374's enrollment target sits among peer trials

1,075 271st of 2000 higher than 1,730 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 NCT00699374, the US trial registry maintained by the National Library of Medicine. NCT00699374 (large enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.