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SAB Biotherapeutics Inc (SABSW) is a clinical-stage biopharmaceutical leader advancing targeted human antibody therapies through its proprietary DiversitAb platform. This page provides investors and researchers with essential updates on clinical developments, financial disclosures, and strategic partnerships.
Access real-time announcements about therapeutic candidates like SAB-142 for type 1 diabetes, manufacturing innovations using transchromosomic cattle, and collaborative research milestones. Our curated news collection ensures you never miss critical updates on regulatory progress or pipeline expansions.
Key content includes earnings reports, trial result announcements, partnership disclosures, and analysis of competitive positioning in immunotherapy markets. All materials are sourced from verified channels to maintain factual accuracy and compliance standards.
Bookmark this page for streamlined access to SAB Biotherapeutics' latest advancements in developing fully human antibodies for autoimmune disorders and infectious diseases. Check regularly for authoritative updates directly impacting the company's trajectory in biopharmaceutical innovation.
SAB Biotherapeutics announced positive top-line results from the Phase 3 NIH ACTIV-2 clinical trial evaluating SAB-185, a human IgG1 antibody therapeutic candidate, in non-hospitalized COVID-19 patients at high risk of severe outcomes. The trial found that 66% of participants receiving SAB-185 achieved full symptom resolution for at least four consecutive days by Day 28, compared to 50% for the REGEN-COV® group (p=0.010). Furthermore, the median time to symptom resolution was significantly shorter for SAB-185, with a reduction of 7 days for 4-day resolution and 6 days for 2-day resolution. However, the primary endpoint regarding hospitalizations and deaths was inconclusive due to the low number of clinical events following the emergence of the Omicron variant. The trial was halted based on recommendations from the Data and Safety Monitoring Board.
SAB Biotherapeutics announced that its investigational therapeutic, SAB-176, has received both Breakthrough Therapy and Fast Track designations from the FDA for treating high-risk patients and post-exposure prophylaxis of Type A and B influenza. This dual designation could significantly expedite its development and regulatory process. SAB-176, a fully-human multi-epitope binding antibody, shows promise against antiviral-resistant strains of influenza. The company is poised to initiate a Phase 2b trial after receiving FDA guidance, highlighting its clear regulatory pathway for further development. The therapy aims to offer broad protection against evolving influenza strains, potentially addressing significant health concerns globally.
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