View source for Ovarian Cancer Trials

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|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''S.No.'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Drug Name'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Biological Name'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Developer'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Current Development Phase'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Additional Information'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Start Date'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Completion Date'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Source'''</font>
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|align = "center" bgcolor = "#DBE5F1"|11
|align = "center" bgcolor = "#DBE5F1"|<nowiki>-</nowiki>
|bgcolor = "#DBE5F1"|DPX-0907
|bgcolor = "#DBE5F1"|ImmunoVaccine Technologies, Inc.
|align = "center" bgcolor = "#DBE5F1"|I
|bgcolor = "#DBE5F1"|To determine the safety and immunogenicity profile of two (2) different doses of the vaccine DPX-0907 to treat breast, ovarian and prostate cancer.
|bgcolor = "#DBE5F1"|2010
|bgcolor = "#DBE5F1"|2011
|bgcolor = "#DBE5F1"|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show?term=cancer+vaccine&rank=55 Source]</u></font>
|-
|align = "center"|12
|align = "center"|<nowiki>-</nowiki>
|ALVAC-hB7.1,  recombinant interferon gamma
|M.D. Anderson Cancer Center, National Cancer Institute (NCI)
|align = "center"|I
|Phase I trial to study the effectiveness of a tumor cell vaccine and interferon gamma in patients with refractory epithelial ovarian cancer.
|1997
|Ongoing
|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show/NCT00004032?term=cancer+vaccine&rank=37 Source]</u></font>
|-
|align = "center" bgcolor = "#DBE5F1"|13
|align = "center" bgcolor = "#DBE5F1"|<nowiki>-</nowiki>
|bgcolor = "#DBE5F1"|PSMA/PRAME
|bgcolor = "#DBE5F1"|MannKind Corporation
|align = "center" bgcolor = "#DBE5F1"|I
|bgcolor = "#DBE5F1"|The present clinical trial is a dose comparison of a multi-component active immunotherapy designed to stimulate an immune reaction to specific tumor associated antigens which are highly expressed on a large number of solid cancers.
|bgcolor = "#DBE5F1"|2007
|bgcolor = "#DBE5F1"|2009
|bgcolor = "#DBE5F1"|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show/NCT00423254?term=MKC1106-PP&rank=1 Source]</u></font>
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|align = "center"|14
|align = "center"|<nowiki>-</nowiki>
|PSMA/PRAME
|MannKind Corporation
|align = "center"|I
|Completed<br>The present clinical trial is a dose comparison of a multi-component active immunotherapy designed to stimulate an immune reaction to specific tumor associated antigens which are highly expressed on a large number of solid cancers.
|2007
|2009
|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show/NCT00423254?term=MKC1106-PP&rank=1 Source]</u></font>
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|align = "center" bgcolor = "#DBE5F1"|15
|align = "center" bgcolor = "#DBE5F1"|<nowiki>-</nowiki>
|bgcolor = "#DBE5F1"|Abagovomab
|bgcolor = "#DBE5F1"|Menarini Group
|align = "center" bgcolor = "#DBE5F1"|II/III
|bgcolor = "#DBE5F1"|The purpose of this study is to evaluate the benefit of vaccination with Abagovomab, an experimental immunotherapy in ovarian cancer patients. The benefit will be evaluated in terms of time the remission status is kept as well as prolongation of life expectancy.
|bgcolor = "#DBE5F1"|2006
|bgcolor = "#DBE5F1"|2015
|bgcolor = "#DBE5F1"|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show/NCT00418574?term=Abagovomab&rank=1 Source]</u></font>
|-
|align = "center"|16
|align = "center"|<nowiki>-</nowiki>
|Interleukin-2
|National Cancer Institute (NCI)
|align = "center"|II
|Phase II trial to study the effectiveness of a vaccine made with the patients<nowiki>’</nowiki> white blood cells mixed with tumor proteins in treating patients who have advanced cancer.
|align = "center"|<nowiki>-</nowiki>
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|align = "center" bgcolor = "#DBE5F1"|17
|align = "center" bgcolor = "#DBE5F1"|<nowiki>-</nowiki>
|bgcolor = "#DBE5F1"|DCVax-Ovarian
|bgcolor = "#DBE5F1"|Northwest Biotherapeutics
|align = "center" bgcolor = "#DBE5F1"|I
|align = "center" bgcolor = "#DBE5F1"|<nowiki>-</nowiki>
|align = "center" bgcolor = "#DBE5F1"|<nowiki>-</nowiki>
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|align = "center"|18
|align = "center"|<nowiki>-</nowiki>
|MUC1 Dendritic Cell Vaccine (Cvac)
|Prima BioMed Ltd
|align = "center"|II
|The purpose of this study is to determine the safety and efficacy of an investigational vaccine in ovarian cancer patients in remission and to determine its ability to prevent cancer from returning.
|2010
|2013
|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show?term=cancer+vaccine&rank=47 Source]</u></font>
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|align = "center" bgcolor = "#DBE5F1"|19
|bgcolor = "#DBE5F1"|carboplatin, paclitaxel
|bgcolor = "#DBE5F1"|MAGE-A1, Her-2/neu, FBP peptides ovarian cancer vaccine; tetanus toxoid helper peptide
|bgcolor = "#DBE5F1"|University of Virginia; NCI
|align = "center" bgcolor = "#DBE5F1"|II
|bgcolor = "#DBE5F1"|This phase II trial is studying how well giving vaccine therapy together with paclitaxel and carboplatin works in treating patients who are undergoing surgery for stage III or stage IV ovarian cancer, primary peritoneal cancer, or fallopian tube cancer.
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