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NCT01306630 · ClinicalTrials.gov registry record · Phase 1

A Trial of Tivozanib (AV-951) in Combination With Capecitabine (Xeloda®) in Subjects With Advanced Solid Tumors

A Phase 1 study, sponsored by AVEO Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT01306630 is a Phase 1 study that has completed, run by AVEO Pharmaceuticals. The registered enrollment target is 24 participants.

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The verdict

NCT01306630, a Phase 1 study, has completed, sponsored by AVEO Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

This is an open-label, multi-center, dose-finding study of tivozanib administered in combination with capecitabine. During the dose-escalation portion, sequential cohorts of subjects with advanced solid tumors will be enrolled in order to establish the maximum tolerated dose (MTD). If the MTD is not reached, the recommended Phase 2 dose (RP2D) will be determined. In the expansion cohort, subjects with locally advanced or metastatic breast or colon cancer will be enrolled at MTD (or RP2D) to further evaluate safety and activity of this combination in these tumor types.

Interventions

  • DRUG tivozanib (AV-951) and capecitabine (Xeloda®)

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2010-11
Est. Completion 2014-01
Phase Phase 1

Sponsor

AVEO Pharmaceuticals

27 total trials

What the Registry Record Tells You About NCT01306630

The ClinicalTrials.gov registry entry for NCT01306630 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AVEO Pharmaceuticals, which has 27 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which tivozanib (AV-951) and capecitabine (Xeloda®) is the first listed.

NCT01306630 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01306630 about?

NCT01306630 is a clinical study titled "A Trial of Tivozanib (AV-951) in Combination With Capecitabine (Xeloda®) in Subjects With Advanced Solid Tumors". This is an open-label, multi-center, dose-finding study of tivozanib administered in combination with capecitabine. During the dose-escalation portion, sequential cohorts of subjects with advanced solid tumors will be enrolled in order to establish the maximum tolerated dose (MTD). If the MTD is not...

What is the current status of trial NCT01306630?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2010-11. Estimated completion is 2014-01.

What interventions are being tested in trial NCT01306630?

The interventions under investigation include: tivozanib (AV-951) and capecitabine (Xeloda®) (DRUG).

Who is sponsoring clinical trial NCT01306630?

This trial is sponsored by AVEO Pharmaceuticals, which has 27 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.