Phase II Study of Neoadjuvant Chemotherapy With Doxorubicin Followed by Docetaxel-Cisplatin in Locally Advanced Breast Cancer

Overview[ - collapse ][ - ]

Purpose Phase II study of neoadjuvant chemotherapy with Doxorubicin followed by Docetaxel-Cisplatin in locally advanced breast cancer
ConditionBreast Cancer
InterventionDrug: Doxorubicin, Docetaxel, Cisplatin
PhaseN/A
SponsorKing Faisal Specialist Hospital & Research Center
Responsible PartyKing Faisal Specialist Hospital & Research Center
ClinicalTrials.gov IdentifierNCT00538525
First ReceivedOctober 1, 2007
Last UpdatedMay 26, 2012
Last verifiedMay 2012

Tracking Information[ + expand ][ + ]

First Received DateOctober 1, 2007
Last Updated DateMay 26, 2012
Start DateSeptember 2007
Estimated Primary Completion DateApril 2008
Current Primary Outcome MeasuresEffectiveness [Time Frame: overall] [Designated as safety issue: No]
Current Secondary Outcome MeasuresNot Provided

Descriptive Information[ + expand ][ + ]

Brief TitlePhase II Study of Neoadjuvant Chemotherapy With Doxorubicin Followed by Docetaxel-Cisplatin in Locally Advanced Breast Cancer
Official TitleNot Provided
Brief Summary
Phase II study of neoadjuvant chemotherapy with Doxorubicin followed by Docetaxel-Cisplatin
in locally advanced breast cancer
Detailed DescriptionNot Provided
Study TypeInterventional
Study PhaseN/A
Study DesignIntervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
ConditionBreast Cancer
InterventionDrug: Doxorubicin, Docetaxel, Cisplatin
Doxorubicin, Docetaxel, Cisplatin
Other Names:
Doxorubicin, Docetaxel, Cisplatin
Study Arm (s)Active Comparator: Arm 1
Doxorubicin, Docetaxel, Cisplatin

Recruitment Information[ + expand ][ + ]

Recruitment StatusCompleted
Estimated Enrollment10
Estimated Completion DateApril 2008
Estimated Primary Completion DateApril 2008
Eligibility Criteria
Inclusion Criteria:

- Patients with locally advanced breast cancer

Exclusion Criteria:

- Patients with metastatic breast cancer
GenderBoth
AgesN/A
Accepts Healthy VolunteersNo
ContactsNot Provided
Location CountriesNot Provided

Administrative Information[ + expand ][ + ]

NCT Number NCT00538525
Other Study ID NumbersRAC#2011-022
Has Data Monitoring CommitteeNot Provided
Information Provided ByKing Faisal Specialist Hospital & Research Center
Study SponsorKing Faisal Specialist Hospital & Research Center
CollaboratorsNot Provided
Investigators Principal Investigator: Adnan Ezzat, MD KFSH&RC, Riyadh, Saudi Arabia
Verification DateMay 2012