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OpenTrials
Completed

NCT Number: NCT01418222

FOLFOX/Bevacizumab With Onartuzumab (MetMAb) Versus Placebo as First-Line Treatment in Patients With Metastatic Colorectal Cancer

This randomized, double-blind, placebo-controlled study will evaluate the efficacy and safety of FOLFOX/bevacizumab with onartuzumab (MetMAb) versus placebo as first-line treatment in patients with metastatic colorectal cancer.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Almac Clinical Technologies, San Francisco, California, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients, >/= 18 years of age
  • Histologically or cytologically confirmed adenocarcinoma of the colon or rectum in patients with metastatic (Stage IV) disease
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • Measurable disease by RECIST criteria
  • Adequate organ system function, as defined by protocol

Exclusion criteria

  • Prior systemic or radiation therapy for metastatic colorectal cancer
  • Adjuvant chemotherapy (and/or chemoradiation) for colorectal cancer within 12 months prior to date of diagnosis of metastatic disease
  • Previously untreated brain metastases
  • History of hypersensitivity to active or inactive excipients of any component of treatment, or known dipyrimidine dehydrogenase deficiency
  • Evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation)
  • History of hematemesis or hemoptysis </= 1 months prior to study enrollment
  • Significant cardiovascular disease or disorder
  • History of abdominal fistula or gastrointestinal perforation </= 6 months prior to Day 1
  • Positive for hepatitis B, hepatitis C or HIV infection
  • Other active cancers or history of treatment for invasive cancer within the last 5 years, except for non-melanoma skin cancer

Treatment and study plan

5-FU

Drug

Intravenous repeating dose

FOLFOX regimen

Drug

Intravenous repeating dose

Placebo

Drug

Intravenous repeating dose

bevacizumab [Avastin]

Drug

Intravenous repeating dose

Leucovorin

Drug

Intravenous repeating dose

Onartuzumab [MetMAb]

Drug

Intravenous repeating dose

Primary outcomes

  1. Progression-free survival: time from randomization to tumor progression or death, tumor assessments according to RECIST criteria

    Time frame: up to 4 years

Secondary outcomes

  1. Response rate (complete response + partial response)

    Time frame: up to 4 years

  2. Time to treatment failure: from randomization to treatment discontinuation for any reason including disease progression, treatment toxicity, and death

    Time frame: up to 4 years

  3. Overall survival

    Time frame: up to 4 years

  4. Safety: Incidence of adverse events

    Time frame: up to 4 years

Sponsors and collaborators

Lead sponsor

Genentech, Inc.

Industry

Collaborators

  • SCRI Development Innovations, LLC

Registry information

Official study title

Randomized, Double-Blind, Phase II Study of FOLFOX/Bevacizumab With Onartuzumab (MetMAb) Versus Placebo as First-Line Treatment for Patients With Metastatic Colorectal Cancer

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Aug 17, 2011
Registry last updated
May 30, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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