Fallopian Tube Cancer Clinical Trial
Official title:
A Phase I Study of the Safety and Biological Activity of Intraperitoneal IMNN-001 (IL-12 Plasmid Formulated With PEG-PEI-Cholesterol Lipopolymer) Administered In Combination With Standard Neoadjuvant Chemotherapy in Patients Newly Diagnosed With Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer
This dose escalation study will determine a maximum tolerated dose and/or optimal biological dose of GEN-1 for carboplatin/paclitaxel combination in newly diagnosed ovarian cancer.
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Status | Clinical Trial | Phase | |
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Active, not recruiting |
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Study of IMNN-001 (Also Known as GEN-1) With NACT for Treatment of Ovarian Cancer (OVATION 2)
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Phase 1/Phase 2 | |
Completed |
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Active, not recruiting |
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Phase 2 | |
Completed |
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N/A | |
Completed |
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Active, not recruiting |
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Dual mTorc Inhibition in advanCed/Recurrent Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer (of Clear Cell, Endometrioid and High Grade Serous Type, and Carcinosarcoma)
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Phase 2 | |
Not yet recruiting |
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Phase 2 | |
Completed |
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Phase 2 | |
Completed |
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Phase 1/Phase 2 | |
Completed |
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Phase 2 | |
Completed |
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Neoadjuvant Chemotherapy IV Carboplatin With Weekly Paclitaxel \Bevacizumab for Primary Ovarian
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Phase 1 | |
Completed |
NCT01031381 -
Study of RAD001 and Bevacizumab in Recurrent Ovarian, Peritoneal, and Fallopian Tube Cancer
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Phase 2 | |
Completed |
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Phase 1 | |
Completed |
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N/A | |
Suspended |
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Phase 1 | |
Completed |
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Phase 2 | |
Completed |
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Phase 1 | |
Recruiting |
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Phase 2 | |
Completed |
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Phase 2 | |
Terminated |
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Phase 2 |