{"id":18812,"date":"2022-03-04T08:21:49","date_gmt":"2022-03-04T16:21:49","guid":{"rendered":"https:\/\/marketdepth.com\/?p=18812"},"modified":"2022-03-04T08:21:51","modified_gmt":"2022-03-04T16:21:51","slug":"statera-biopharma-submits-pilot-study-to-u-s-fda","status":"publish","type":"post","link":"https:\/\/marketdepth.com\/statera-biopharma-submits-pilot-study-to-u-s-fda\/","title":{"rendered":"Statera Biopharma Submits Pilot Study to U.S. FDA"},"content":{"rendered":"\n

Statera Biopharma, Inc. (Nasdaq: STAB)<\/strong> recently announced <\/a>that it submitted a pilot study protocol for STAT-205 treatment of post-acute COVID-19 to the U.S. Food and Drug Administration (FDA).<\/p>\n\n\n\n

Pilot Program<\/h5>\n\n\n\n

The Phase 1 pilot study is set to evaluate the Safety and Efficacy of STAT-205 in approximately 84 patients with Post-acute Sequalae of SARS-CoV-2 infection (PASC). Additionally, STAT-205 for acute COVID is currently being evaluated in Phase 1 clinical trial in adult patients with mild COVID-19 who are at high risk of disease progression.<\/p>\n\n\n\n

\u201cSubmitting this study protocol to the FDA is a critical milestone in the development of our COVID-19 program. As the world continues to struggle with the COVID-19 pandemic, post-acute COVID syndrome remains a widespread, often debilitating condition that is not well understood. With STAT-205 Statera looks to potentially offer a promising treatment approach to those patients facing the long-lasting burden of the illness.\u201d<\/p>Michael K. Handley, President and Chief Executive Officer, Statera Biopharma<\/cite><\/blockquote>\n\n\n\n

Persistent fatigue following COVID-19 is one of the most common symptoms, and no standard of care for PASC exists. <\/p>\n","protected":false},"excerpt":{"rendered":"Statera Biopharma, Inc. (Nasdaq: STAB) recently announced that it submitted a pilot study protocol for STAT-205 treatment of post-acute COVID-19 to the U.S. Food and Drug Administration (FDA). Pilot Program The Phase 1 pilot study is set to evaluate the Safety and Efficacy of STAT-205 in approximately 84 patients with Post-acute Sequalae of SARS-CoV-2 infection… View Article<\/a>","protected":false},"author":3,"featured_media":18372,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"pmpro_default_level":0,"footnotes":""},"categories":[9,31,17,8,11,16],"tags":[],"acf":[],"yoast_head":"\nStatera Biopharma Submits Pilot Study to U.S. FDA - MarketDepth<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/marketdepth.com\/statera-biopharma-submits-pilot-study-to-u-s-fda\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Statera Biopharma Submits Pilot Study to U.S. FDA - MarketDepth\" \/>\n<meta property=\"og:description\" content=\"Statera Biopharma, Inc. (Nasdaq: STAB) recently announced that it submitted a pilot study protocol for STAT-205 treatment of post-acute COVID-19 to the U.S. Food and Drug Administration (FDA). Pilot Program The Phase 1 pilot study is set to evaluate the Safety and Efficacy of STAT-205 in approximately 84 patients with Post-acute Sequalae of SARS-CoV-2 infection... 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