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NCT01254526 · ClinicalTrials.gov registry record · Phase 1

Study of the Safety and Pharmacology of GDC-0980 in Combination With Paclitaxel With or Without Bevacizumab in Patients With Locally Recurrent or Metastatic Breast Cancer

A Phase 1 study of Breast Cancer, sponsored by Genentech.

Completed
Registry status
Phase 1
Development phase
52
Enrollment target
3
Study locations

NCT01254526 is a Phase 1 study of Breast Cancer that has completed, run by Genentech. The registered enrollment target is 52 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT01254526, a Phase 1 study of Breast Cancer, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 1
Development phase
52 participants
Enrollment target
3
Study locations

Study Summary

This is an open-label, multicenter, Phase Ib dose-escalation study to assess the safety, tolerability, and pharmacokinetics of GDC-0980 administered with taxane-based chemotherapy regimens utilized in patients with locally recurrent or metastatic breast cancer.

Conditions Studied

Interventions

  • DRUG bevacizumab
  • DRUG paclitaxel
  • DRUG GDC-0980

Study Locations (3)

Massachusetts

  • - Boston

Tennessee

  • - Nashville

Other

  • - Leuven

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2010-12
Est. Completion 2013-04
Phase Phase 1

Sponsor

Genentech

332 total trials

What the Registry Record Tells You About NCT01254526

The ClinicalTrials.gov registry entry for NCT01254526 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The listed sponsor is Genentech, which has 332 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 3 interventions - of which bevacizumab is the first listed.

NCT01254526 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Massachusetts, Tennessee, Other.

Frequently Asked Questions

What is clinical trial NCT01254526 about?

NCT01254526 is a clinical study titled "Study of the Safety and Pharmacology of GDC-0980 in Combination With Paclitaxel With or Without Bevacizumab in Patients With Locally Recurrent or Metastatic Breast Cancer". This is an open-label, multicenter, Phase Ib dose-escalation study to assess the safety, tolerability, and pharmacokinetics of GDC-0980 administered with taxane-based chemotherapy regimens utilized in patients with locally recurrent or metastatic breast cancer.

What is the current status of trial NCT01254526?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 52 participants. The study started on 2010-12. Estimated completion is 2013-04.

What conditions does trial NCT01254526 study?

This clinical trial studies the following conditions: Breast Cancer.

What interventions are being tested in trial NCT01254526?

The interventions under investigation include: bevacizumab (DRUG), paclitaxel (DRUG), GDC-0980 (DRUG).

Who is sponsoring clinical trial NCT01254526?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01254526 being conducted?

This trial has 3 study locations across Massachusetts, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.