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NCT01004978 · ClinicalTrials.gov registry record · Phase 3

Chemoembolization With or Without Sorafenib Tosylate in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery

A Phase 3 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 3
Development phase
235
Enrollment target

NCT01004978: Completed Phase 3 study, sponsored by National Cancer Institute (NCI).

NCT01004978 is a Phase 3 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 235 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01004978, a Phase 3 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 3
Development phase
235 participants
Enrollment target

Study Summary

This randomized phase III trial studies chemoembolization and sorafenib tosylate to see how well they work compared with chemoembolization alone in treating patients with liver cancer that cannot be removed by surgery. Drugs used in chemotherapy, such as doxorubicin hydrochloride, mitomycin, and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Chemoembolization kills tumor cells by carrying drugs directly into blood vessels near the tumor and then blocking the blood flow to allow a higher concentration of the drug to reach the tumor for a longer period of time. Kinase inhibitors, such as sorafenib tosylate may stop the growth of tumor cells by blocking the action of an abnormal protein that signals cancer cells to multiply. It is not yet known whether giving chemoembolization together with sorafenib tosylate is more effective than chemoembolization alone in treating patients with liver cancer.

Primary Outcome

PFS is defined to be the time from randomization to progression or death without evidence of progression. For cases without documentation of progression, follow-up will be censored at the date of last disease assessment without progression, unless death occurs within 4 months following the date last known progression-free, in which case the death will be counted as an event. Progression is assessed per Solid Tumor Response Criteria (RECIST) and defined as at least a 20% increase in the sum of t

Interventions

  • PROCEDURE Computed Tomography
  • DRUG Cisplatin
  • OTHER Laboratory Biomarker Analysis
  • DRUG Doxorubicin Hydrochloride
  • DRUG Doxorubicin-Eluting Beads

Trial Details

FieldValue
Enrollment Target 235 participants
Start Date 2009-10-28
Est. Completion 2022-12-21
Phase Phase 3
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT01004978 record still lists

NCT01004978 is an interventional study that assigns participants to a tested intervention. The registered 235 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 5 interventions - of which Computed Tomography is the first listed.

NCT01004978 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01004978 about?

NCT01004978 is a clinical study titled "Chemoembolization With or Without Sorafenib Tosylate in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery". This randomized phase III trial studies chemoembolization and sorafenib tosylate to see how well they work compared with chemoembolization alone in treating patients with liver cancer that cannot be removed by surgery. Drugs used in chemotherapy, such as doxorubicin hydrochloride, mitomycin, and cis...

What is the current status of trial NCT01004978?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 235 participants. The study started on 2009-10-28. Estimated completion is 2022-12-21.

What interventions are being tested in trial NCT01004978?

The interventions under investigation include: Computed Tomography (PROCEDURE), Cisplatin (DRUG), Laboratory Biomarker Analysis (OTHER), Doxorubicin Hydrochloride (DRUG), Doxorubicin-Eluting Beads (DRUG).

Who is sponsoring clinical trial NCT01004978?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01004978's enrollment target sits among peer trials

235 1296th of 2000 higher than 704 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 NCT01004978, the US trial registry maintained by the National Library of Medicine. NCT01004978 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.