{"id":452,"date":"2026-01-16T12:46:57","date_gmt":"2026-01-16T11:46:57","guid":{"rendered":"https:\/\/ced-studienzentrum.berlin\/2026\/01\/16\/crohns-disease-sar441566-study-study-partner\/"},"modified":"2026-02-03T11:03:07","modified_gmt":"2026-02-03T10:03:07","slug":"crohns-disease-sar441566-study-study-partner","status":"publish","type":"post","link":"https:\/\/ced-studienzentrum.berlin\/en\/crohns-disease-sar441566-study-study-partner\/","title":{"rendered":"Crohn&#8217;s Disease: SAR441566 Study \u2013 Study Partner"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; admin_label=&#8221;Listings&#8221; module_id=&#8221;target group&#8221; _builder_version=&#8221;4.27.5&#8243; _module_preset=&#8221;default&#8221; background_color=&#8221;#FFFFFF&#8221; background_enable_image=&#8221;off&#8221; background_size=&#8221;custom&#8221; background_image_width=&#8221;90%&#8221; background_position=&#8221;bottom_right&#8221; custom_padding=&#8221;||0px|||&#8221; top_divider_height=&#8221;51px&#8221; locked=&#8221;off&#8221; collapsed=&#8221;on&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_row use_custom_gutter=&#8221;on&#8221; gutter_width=&#8221;3&#8243; _builder_version=&#8221;4.27.5&#8243; _module_preset=&#8221;default&#8221; width=&#8221;100%&#8221; custom_margin=&#8221;||30px||false|false&#8221; custom_padding=&#8221;||0px||false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.18.0&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_post_title meta=&#8221;off&#8221; featured_image=&#8221;off&#8221; _builder_version=&#8221;4.27.5&#8243; _module_preset=&#8221;default&#8221; title_text_color=&#8221;#10344C&#8221; title_font_size=&#8221;45px&#8221; custom_margin=&#8221;||15px|||&#8221; global_colors_info=&#8221;{}&#8221; theme_builder_area=&#8221;post_content&#8221;][\/et_pb_post_title][et_pb_text _builder_version=&#8221;4.27.5&#8243; _module_preset=&#8221;1f09816e-184e-4ce5-a4cf-b39c52c423ca&#8221; text_font=&#8221;&#8211;et_global_body_font||||||||&#8221; text_text_color=&#8221;#10344C&#8221; text_font_size=&#8221;20px&#8221; text_line_height=&#8221;1.8em&#8221; ul_line_height=&#8221;1.8em&#8221; custom_margin=&#8221;||||false|false&#8221; text_font_size_tablet=&#8221;15px&#8221; text_font_size_phone=&#8221;14px&#8221; text_font_size_last_edited=&#8221;on|phone&#8221; header_font_size_tablet=&#8221;55px&#8221; header_font_size_last_edited=&#8221;off|desktop&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>A study to investigate the efficacy and safety of SAR441566 in patients with Crohn&#8217;s disease (SPECIFI-CD)<\/h3>\n<p><strong>ClinicalTrials.gov ID:<\/strong> NCT06637631<br \/><strong>Sponsor:<\/strong> Sanofi (Information provided by Sanofi (responsible party))<\/p>\n<h3>Study overview<\/h3>\n<p><strong>Official title: <\/strong>A multinational, multicenter, randomized, double-blind, placebo-controlled, Phase 2 dose-ranging study to evaluate the efficacy and safety of SAR441566 in adults with moderate to severe Crohn&#8217;s disease.<\/p>\n<h3>Brief summary<\/h3>\n<p>This is a Phase 2 study that is multinational, multicenter, randomized, double-blind, placebo-controlled, and dose-ranging to investigate the efficacy and safety of SAR441566 in adults with moderate to severe Crohn&#8217;s disease (CD).<\/p>\n<p>The primary objective of this study is to evaluate the efficacy of different dosages of SAR441566 compared to placebo in participants with moderate to severe Crohn&#8217;s disease.<\/p>\n<p>The estimated total duration of the study is up to 59 weeks. This includes: <\/p>\n<ul>\n<li>a screening phase of 4 weeks (plus up to 7 calendar days if required),<\/li>\n<li>followed by the main study treatment phase lasting 52 weeks,<\/li>\n<li>as well as a 2-week follow-up phase after the end of treatment.<\/li>\n<\/ul>\n<p>The main study phase includes a double-blind treatment phase with 12 weeks of induction, followed by 40 weeks of maintenance therapy.<\/p>\n<p>In addition, eligible participants will be offered an open-label treatment phase of up to 40 weeks. The combined duration of the double-blind maintenance phase and the open-label treatment phase must not exceed 40 weeks in total, depending on when the participants switch. <\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A study to investigate the efficacy and safety of SAR441566 in patients with Crohn&#8217;s disease (SPECIFI-CD) ClinicalTrials.gov ID: NCT06637631Sponsor: Sanofi (Information provided by Sanofi (responsible party)) Study overview Official title: A multinational, multicenter, randomized, double-blind, placebo-controlled, Phase 2 dose-ranging study to evaluate the efficacy and safety of SAR441566 in adults with moderate to severe Crohn&#8217;s [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"categories":[40,36],"tags":[],"class_list":["post-452","post","type-post","status-publish","format-standard","hentry","category-active-searching","category-for-study-partners"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.9 - 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