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Study Title: Weekly IV of Hymcamtin in Combination with Carboplatin as Second Line Therapy in Potentially Platinum-Sensitive Reaplased Ovarian Cancer
Category: Cancer, General
Currently accepting participants?
Not at this time.
Principal Investigator: Thomas Malpass
Study Coordinator: Kathy Rabena
Phone: (206) 223-6892 Ext.36892
Email: Katherine.Rabena@vmmc.org
What is the Weekly IV of Hymcamtin in Combination with Carboplatin as Second Line Therapy in Potentially Platinum-Sensitive Reaplased Ovarian Cancer study?
An Open Label, Single-Arm, Phase II Study of IV Weekly (Days 1 and 8 eery 21 Days)Hymcantin in Combination with Carboplatin(Day 1 every 21 dys) as Second-Line Therapy in Subjects with Potemtially Platinum-Sensitive Relapsed Ovarian Cancer
Who can participate?
Eligibility:
~Patients with recurrent epithelial ovarin, fallopian tube, or primary peritoneal cancer.
~Has received one prior platinum-based chemotherapeutic regimen (containing either carboplatin or cisplatin) for the treatment of primary disease.
~Patient's disease is considered potentially platinum-sensitive.
~Must have atleast one measurable lesion as determined by diagnostic studies including CT or MRI or physical exam.
Ineligibility:
~Pregnant or lactating
~Received morn that 1 prior chemotherapy regimen or a histery of consolidation cytotoxic chemotherapy
~Has brain metasteses
~Received prior treatment with Hymcantin
What do I have to do as a study participant?
Study Summary:
An Open Label, Single-Arm, Phase II Study of IV Weekly (Days 1 and 8 eery 21 Days)Hymcantin in Combination with Carboplatin(Day 1 every 21 dys) as Second-Line Therapy in Subjects with Potemtially Platinum-Sensitive Relapsed Ovarian Cancer
Detailed Study Description:
(No information)
Study Design: Interventional
Phase of Study: Phase II
Study Type: Interventional
Condition or Study Focus: Ovarian Cancer
Intervention Type: Chemotherapy
Intervention Name: Hymcantin
Gender: Female
Age group: Interventional
Sponsor: GlaxoSmithKline
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