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Demonstrate Efficacy and Safety of Metastatic Breast Cancer (Compare)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01084876
Recruitment Status : Unknown
Verified February 2015 by Celltrion.
Recruitment status was:  Active, not recruiting
First Posted : March 11, 2010
Last Update Posted : February 12, 2015
Information provided by (Responsible Party):

Brief Summary:
The purpose of the study is to to demonstrate equivalence

Condition or disease Intervention/treatment Phase
Metastatic Breast Cancer Drug: CT-P6 Drug: Herceptin Drug: Paclitaxel Phase 3

Detailed Description:
Patients will receive study drug every 3 weeks.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 383 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Official Title: Double-blind, Randomised, Parallel Group, Phase III Study
Study Start Date : June 2010
Actual Primary Completion Date : December 2011
Estimated Study Completion Date : December 2017

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Active Comparator: CT-P6 & Paclitaxel
CT-P6 + Paclitaxel
Drug: CT-P6
Administered every 3 weeks

Drug: Paclitaxel
Administered every 3weeks

Active Comparator: Herceptin & Paclitaxel
Trastuzumab + Paclitaxel
Drug: Herceptin
Administered every 3 weeks
Other Name: Trastuzumab

Drug: Paclitaxel
Administered every 3weeks

Primary Outcome Measures :
  1. To Compare Efficacy [ Time Frame: months ]

Secondary Outcome Measures :
  1. efficacy and safety [ Time Frame: months ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Are females
  • Have a Her 2 over-expression
  • Have ECOG 0 or 1

Exclusion Criteria:

  • Current clinical or radiographic evidence CNS metastases
  • Current Known infection
  • Pregnant or nursing mother

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01084876

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Investigational Site
Baia-mare, Romania
Sponsors and Collaborators
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Principal Investigator: Investigational Site Samsung Medical Center
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Responsible Party: Celltrion Identifier: NCT01084876    
Other Study ID Numbers: CT-P6/3.1
First Posted: March 11, 2010    Key Record Dates
Last Update Posted: February 12, 2015
Last Verified: February 2015
Keywords provided by Celltrion:
metastatic breast cancer
Additional relevant MeSH terms:
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Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases
Antineoplastic Agents, Phytogenic
Antineoplastic Agents
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents, Immunological