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Randomized phase III trial of cisplatin plus paclitaxel with and without NCI-supplied bevacizumab (NSC #704865, IND #7921) versus the non-platinum doublet, topotecan plus paclitaxel, with and without NCI-supplied bevacizumab, in stage IVB, recurrent or persistent carcinoma of the cervix
eagle-i ID
http://hawaii.eagle-i.net/i/00000130-dd8d-f6d7-9953-50a980000000
Resource Type
Properties
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ClinicalTrials.gov url
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http://www.clinicaltrials.gov/ct2/show/NCT00803062?term=GOG-0240&rank=1
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Intervention
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Cisplatin
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Intervention
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Paclitaxel
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Intervention
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Topotecan hydrochloride
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Intervention
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Bevacizumab
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Additional Topic(s)
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Antineoplastic combined chemotherapy protocols
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Resource Description
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Purpose: It is not yet known whether paclitaxel is more effective when given together with cisplatin or topotecan with or without bevacizumab in treating patients with cervical cancer.
This randomized phase III trial is studying the side effects of paclitaxel when given together with cisplatin or topotecan with or without bevacizumab and to compare how well they work in treating patients with stage IVB, recurrent, or persistent cervical cancer.
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Contact
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Berenberg, Jeffrey
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PI
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Berenberg, Jeffrey
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Topic
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cervix carcinoma
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Study Population
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Females age 18 and older with measurable disease, no primary brain tumor, brain metastases, or spinal cord metastases, no previous bevacizumab, at least 6 weeks since chemotherapy with radiation therapy, at least 3 weeks since radiation therapy, and more than 4 weeks since surgery or open biopsy.
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Website(s)
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http://www.cancer.gov/clinicaltrials/search/view?cdrid=628746&version=healthprofessional
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Funded by
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Gynecologic Oncology Group
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Phase
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Phase 3 clinical trial
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Performed by
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Clinical Protocol & Data Management Shared Resource
