{"id":829,"date":"2021-02-12T09:16:32","date_gmt":"2021-02-12T08:16:32","guid":{"rendered":"https:\/\/ago-ovar.de\/profile\/open-trials\/"},"modified":"2026-04-08T14:34:26","modified_gmt":"2026-04-08T12:34:26","slug":"open-trials","status":"publish","type":"page","link":"https:\/\/ago-ovar.de\/en\/profile\/open-trials\/","title":{"rendered":"Open Trials"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; specialty=&#8221;on&#8221; _builder_version=&#8221;4.16&#8243; background_color=&#8221;#e0edf9&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;3_4&#8243; specialty_columns=&#8221;3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_row_inner _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;||13px|||&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; text_text_color=&#8221;#000000&#8243; header_font=&#8221;|700||on|||||&#8221; header_text_color=&#8221;#11487E&#8221; header_2_text_color=&#8221;#11487E&#8221; custom_margin=&#8221;||8px|||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h1>Open Trials<\/h1>\n<p>[\/et_pb_text][et_pb_text _builder_version=&#8221;4.16&#8243; text_text_color=&#8221;#000000&#8243; header_font=&#8221;|700||on|||||&#8221; header_text_color=&#8221;#11487E&#8221; header_2_text_color=&#8221;#11487E&#8221; header_2_font_size=&#8221;24px&#8221; custom_margin=&#8221;||8px|||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Ovary<\/h2>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;5%|6%|5%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.19.5&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_3_font=&#8221;|700|||||||&#8221; header_3_text_color=&#8221;#7ca9d6&#8243; header_3_font_size=&#8221;20px&#8221; background_enable_color=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>AGO-OVAR 27 \/ WoO<\/h3>\n<p>Window-of-opportunity proof-of-concept, non-randomized, open-label, phase II trial of Olaparib given alone (cohort A) or in combination with Durvalumab (cohort B) prior to primary debulking surgery in histologically proven high-grade epithelial ovarian cancer (EOC)<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][et_pb_button button_url=&#8221;https:\/\/ago-ovar.de\/wp-content\/uploads\/2023\/05\/AGO-OVAR-27_WoO_Synopsis_V07F_2023-02-27.pdf&#8221; url_new_window=&#8221;on&#8221; button_text=&#8221;DOWNLOAD AGO-OVAR 27 SYNOPSIS&#8221; _builder_version=&#8221;4.20.2&#8243; custom_button=&#8221;on&#8221; button_text_size=&#8221;18px&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_button][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;5%|6%|5%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.18.0&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_3_font=&#8221;|700|||||||&#8221; header_3_text_color=&#8221;#7ca9d6&#8243; header_3_font_size=&#8221;20px&#8221; background_enable_color=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>AGO-OVAR 28<\/h3>\n<p>Niraparib vs Niraparib in combination with Bevacizumab in patients with carboplatinum-taxane based chemotherapy in advanced ovarian cancer (A multicentre randomised phase III trial)<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][et_pb_button button_url=&#8221;https:\/\/ago-ovar.de\/wp-content\/uploads\/2025\/07\/AGO-OVAR-28_Synopse_DE_V04F_2025-05-22_clean.pdf&#8221; url_new_window=&#8221;on&#8221; button_text=&#8221;DOWNLOAD AGO-OVAR 28 German synopsis&#8221; _builder_version=&#8221;4.27.4&#8243; custom_button=&#8221;on&#8221; button_text_size=&#8221;18px&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_button][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;5%|6%|5%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.27.4&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_3_font=&#8221;|700|||||||&#8221; header_3_text_color=&#8221;#7ca9d6&#8243; header_3_font_size=&#8221;20px&#8221; background_enable_color=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>AGO-OVAR 2.44 \/ GLORIOSA<\/h3>\n<p>Randomized, multicenter, open-label, Phase 3 study of mirvetuximab soravtansine in combination with bevacizumab versus bevacizumab alone as maintenance therapy for patients with FR\u03b1-high recurrent platinum-sensitive epithelial ovarian, fallopian tube, or primary peritoneal cancers who have not progressed after second-line platinum-based chemotherapy plus bevacizumab (GLORIOSA)<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][et_pb_button button_url=&#8221;https:\/\/ago-ovar.de\/wp-content\/uploads\/2025\/03\/AGO-OVAR-2.44-GLORIOSA_Synopse-deutsch.pdf&#8221; 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background_enable_color=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>AGO-OVAR 2.46 \/ RAMP 301<\/h3>\n<p>A Study of Avutometinib (VS-6766) + Defactinib (VS-6063) in Recurrent Low-Grade Serous Ovarian Cancer (RAMP 301)<\/p>\n<p><a href=\"https:\/\/clinicaltrials.gov\/study\/NCT06072781\">https:\/\/clinicaltrials.gov\/study\/NCT06072781<\/a><\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.27.4&#8243; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;5%|6%|5%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.27.4&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_3_font=&#8221;|700|||||||&#8221; header_3_text_color=&#8221;#7ca9d6&#8243; header_3_font_size=&#8221;20px&#8221; background_enable_color=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>AGO-OVAR 2.48 \/ RAINFOL-OV2<\/h3>\n<p>A Phase 3 Randomized, Open-label Study of Rinatabart Sesutecan (Rina-S) versus Treatment of Investigator\u2019s Choice in Patients with Platinum Resistant Ovarian Cancer<\/p>\n<p><a href=\"https:\/\/clinicaltrials.gov\/study\/NCT06619236\" target=\"_blank\" rel=\"noopener\">https:\/\/clinicaltrials.gov\/study\/NCT06619236<\/a><\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;52px|||||&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.20.2&#8243; text_text_color=&#8221;#000000&#8243; header_font=&#8221;|700||on|||||&#8221; header_text_color=&#8221;#11487E&#8221; header_2_text_color=&#8221;#11487E&#8221; header_2_font_size=&#8221;24px&#8221; custom_margin=&#8221;||8px|||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Endometrium \/ Vulva \/ Cervix<\/h2>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;4.8%|6%|4.8%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.27.4&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_3_font=&#8221;|700|||||||&#8221; 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_builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.20.2&#8243; text_text_color=&#8221;#000000&#8243; header_font=&#8221;|700||on|||||&#8221; header_text_color=&#8221;#11487E&#8221; header_2_text_color=&#8221;#11487E&#8221; header_2_font_size=&#8221;24px&#8221; custom_margin=&#8221;||8px|||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Surgical and translational issues<\/h2>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.16&#8243; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;5%|6%|5%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.27.0&#8243; 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background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;||32px|||&#8221; custom_padding=&#8221;5%|6%|5%|6%|true|true&#8221; animation_style=&#8221;slide&#8221; animation_direction=&#8221;bottom&#8221; animation_starting_opacity=&#8221;12%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.27.6&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_3_font=&#8221;|700|||||||&#8221; header_3_text_color=&#8221;#7ca9d6&#8243; header_3_font_size=&#8221;20px&#8221; background_enable_color=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>TUBA-WISP-II<\/h3>\n<p>TUBectomy with delayed oophorectomy as Alternative for risk-reducing salpingo-oophorectomy in high-risk Women to assess the Safety of Prevention: TUBA-WISP II<\/p>\n<p>[\/et_pb_text][et_pb_button button_url=&#8221;https:\/\/ago-ovar.de\/wp-content\/uploads\/2026\/04\/TUBA-WISP-II_Synopse_V01F_2025-03-11.pdf&#8221; 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