Emendo Biotherapeutics, Inc.

/ Press release May 31, 2024 SÖDERTÄLJE, SWEDEN, 31 May 2024 – Anocca AB, a leading T cell receptor-engineered T cell (TCR-T) cellular therapeutics company, announces the appointment of Christiane Hanke-Harloff to its Board of Directors. With a distinguished career spanning the biotechnology, pharmaceutical, and CDMO sectors, Christiane Hanke-Harloff brings a wealth of expertise and strategic insights. Christiane is currently a Board member of InnoCore Pharmaceuticals BV and Ascenion GmbH, former Board member of Recipharm AB and also serves as an advisor for lifescience sector investors and biotech firms. Previously held executive roles at Gilead Sciences, Gedeon Richter and other biotech companies, where she was responsible for organisational strategy and the expansion of international business units. She earned her PhD in molecular biology from the Max Planck Institute of Biochemistry in Martinsried, Germany. "We’re pleased to welcome Christiane Hanke-Harloff to Anocca's board. Her extensive experience and deep understanding of the industry and CDMO landscape will be invaluable as we navigate our clinical development and manufacturing expansion," said Hans Stråberg, Anocca’s Chairman of the Board. "Christiane's appointment comes at a pivotal time for Anocca," noted Reagan Jarvis, Co-founder and CEO of Anocca. "Her industry experience will play a valuable supportive role as we progress our TCR-T cell therapies into clinical development for hard-to-treat cancers.” Christiane Hanke-Harloff stated, "Anocca's innovative approach and comprehensive capabilities spanning research to manufacturing position it as a leader in TCR-T cell therapy. I am excited to collaborate with the team as we advance these groundbreaking therapies into clinical development." Anocca has been making significant developments in advancing precision TCR-T cell therapies aimed at transforming patient outcomes in hard-to-treat solid tumor indications. With recent achievements including the licensing agreement for use of EmendoBio’s novel gene editing technology, and by securing GMP license for the largest cell-therapy manufacturing facility in the Nordics, the company is accelerating its journey from discovery to clinical development. Anocca is a fully integrated biopharmaceutical company developing libraries of T cell receptor-engineered T cell (TCR-T) therapies to redefine the treatment of solid tumours and other difficult to treat diseases, including infectious and autommune diseases. Its proprietary technologies have been designed to vastly expand TCR-T cell therapy development, allowing the systematic generation of treatments for the broadest patient populations that equip the immune system against the most difficult to treat solid tumours. Anocca operates an advanced research and development infrastructure, underpinned by a custom software ecosystem and in-house clinical manufacturing and process development facilities. Its unique discovery platform uses programmable human cells to recreate and manipulate T cell immunity. Follow Anocca on LinkedIn and visit our new website Anocca AB Jacob Michlewicz, CFO media@anocca.com Scius Communications (for Anocca AB) Katja Stout Tel: +44 7789 435 990 katja@sciuscommunications.com Daniel Gooch Tel: +44 7747 875 479 daniel@sciuscommunications.com

Fast Track Designation underscores the high unmet medical need for treatment and prevention of acute respiratory distress syndrome (ARDS) TORONTO--(BUSINESS WIRE)-- Vasomune Therapeutics, Inc., has announced today that the US Food and Drug Administration (FDA) granted Fast Track designation for AV-001 for the prevention or treatment of moderate-to-severe ARDS in patients hospitalized with viral and/or bacterial respiratory infections. AV-001 is a first-in-class fully synthetic PEGylated peptide targeting the Tie2 receptor which plays a critical role in vascular stability, barrier integrity and endothelial quiescence, particularly within the pulmonary space. Fast track designation represents a significant regulatory milestone and has been granted based on the potential for AV-001 to address an unmet medical need in ARDS, a global disease characterized by extremely high mortality rates, reaching up to 46% in patients with severe cases. Data from the Phase 1 study established safety, a pharmacokinetic pro to once-daily dosing and Tie2 activation demonstrating strong on-target activity. With the co-development support of AnGes Inc., AV-001 is currently in a Phase 2a clinical trial for prevention and treatment of ARDS in pneumonia and is actively recruiting. “Vasomune is focused on the persisting unmet needs of people grappling with ARDS and other diseases driven by vascular endothelial instability,” said Dr. Brian Jahns, President and Chief Operating Officer. “Vasomune is indebted to the United States Department of Defense Congressionally Directed Medical Research Programs award #PR191212 for support to advance AV-001 to the clinic and award #PR203503 for support to research AV-001 in Phase 2a. Vasomune is also grateful to the National Research Council of Canada Industrial Research Assistance Program for providing research and development funding which supported the Phase 1 study.” Ei Yamada, President & CEO of AnGes, said that “The FDA’s support of expedited development marks another important milestone in our endeavor to change the treatment paradigm with AV-001. We look forward to future success with the Phase 2a study, AV001-004.” About AV-001 Originally discovered and designed at Sunnybrook Research Institute at Sunnybrook Hospital in Toronto, AV-001 is being developed by Vasomune Therapeutics, Inc. under a co-development agreement with AnGes, Inc. [TYO: 4563]. AV-001 is a novel investigational medicine that targets the Tie2 receptor, a transmembrane protein most highly expressed on the surface of endothelial cells in the vasculature. AV-001 activates the nonredundant Tie2-Angiopoietin signaling axis, and through stimulation of multiple downstream pathways normalizes the vasculature by enhancing endothelial cell stability, restoring normal barrier defense, and blocking vascular leak. Vascular dysfunction contributes to the underlying disease pathophysiology in patients with bacterial and viral acute respiratory distress syndrome, sepsis, hemorrhagic shock, acute kidney injury, stroke, and vascular dementia. Importantly, in multiple pre-clinical studies AV-001 tightened endothelial cell-cell junctions and promoted endothelial cell survival, which reduced pulmonary edema, and improved lung function compared to untreated controls translating into significantly improved survival. About Vasomune Therapeutics, Inc. Vasomune Therapeutics, Inc. is a private clinical-stage biopharmaceutical company developing the next generation of medicines to harness the body’s ability to defend against illness. Founded in 2014, Vasomune has focused on vascular normalization strategies, and has progressed the lead candidate AV-001 from bench to bedside. Vascular dysfunction is associated with the pathology of several disease states, including bacterial and viral acute respiratory distress syndrome, sepsis, hemorrhagic shock, acute kidney injury, stroke, and vascular dementia. Vasomune’s corporate headquarters and laboratories are located in Toronto, Canada with US offices in Raleigh, NC. For more information about the company please visit . About AnGes, Inc. AnGes, Inc., a biopharmaceutical company founded in December 1999, focuses on the development of gene-based medicines. In March 2019, AnGes obtained conditional and time-limited approval for its lead product, Collategene® (Hepatocyte Growth Factor; HGF—plasmid gene therapy), for the treatment of lower limb ischemic ulcers. In September 2019, AnGes commenced commercialization in Japan of Collategene®, the world’s first marketed drug using plasmid DNA. AnGes is currently working on the development of a Tie2 tyrosine kinase receptor agonist (AV-001) for COVID-19, viral and bacterial-associated pneumonia and an NF-κB decoy oligonucleotide for chronic discogenic lumbar back pain. Furthermore, AnGes acquired EmendoBio in December 2020 to expand its capabilities in genome-editing technologies. For more information, visit .

Late-Breaking scientific poster at the American Thoracic Society Clinical and Scientific sessions will present Vasomune’s Phase 1 safety, and pharmacokinetic and pharmacodynamic data for AV-001 TORONTO--(BUSINESS WIRE)-- Vasomune Therapeutics Inc., a clinical-stage biopharmaceutical company focused on the development of AV-001 for the treatment of diseases associated with vascular dysfunction, today announced that the Company will present a Late-Breaking scientific poster at the upcoming 2024 American Thoracic Society (ATS) International Conference taking place May 17-22, 2024, at the Manchester Grand Hyatt, San Diego, CA. Vasomune’s lead drug candidate AV-001, codeveloped with AnGes Inc, is a first-in-class fully synthetic PEGylated peptide targeting the Tie2 receptor. Activation of the Tie2 receptor plays a critical role in promoting vascular stability, barrier integrity and endothelial quiescence. Activation of the Tie2 receptor by AV-001 has demonstrated therapeutic potential for the treatment of pneumonia and acute respiratory distress syndrome resulting from infection by SARS-CoV-2 or other viral or bacterial pathogens. AV-001 is currently being researched in NCT05123755, a Phase 2a study for patients hospitalized with pneumonia. “Peer-reviewed presentation of our Phase 1 development data is an important landmark in our development efforts for AV-001” said Dr. Brian E. Jahns, President and Chief Operating Officer. “Vasomune is grateful to the National Research Council Canada for grant #IRAP-965762 which supported the Phase 1 study. Vasomune is also indebted to the United States Department of Defense Congressionally Directed Medical Research Programs award #PR191212 for support to advance AV-001 into the clinic.” Ei Yamada, President & CEO of AnGes, said that “Our Phase 1 trial, NCT04737486, demonstrates that the safety, pharmacokinetics, and pharmacodynamics of AV-001 support further development. We look forward to future success with AV-001.” Clinical and Scientific Sessions Date: May 21, 2024 Presentation Time: 11:30 AM – 1:15 PM PT Session (C40): ARDS and Acute Respiratory Failure: Mechanism, Risk and Outcomes Poster: 14798 - A Randomized, Double‑Blind, Placebo‑Controlled Phase 1 Single and Multiple‑Dose Pharmacokinetic First‑In‑Human Study of AV‑001 in Healthy Subjects for the Treatment of Acute Respiratory Distress Syndrome A copy of the presentation materials can be accessed by visiting after the conclusion of the ATS Conference. About AV-001 Originally discovered and designed at Sunnybrook Research Institute at Sunnybrook Hospital in Toronto, AV-001 is being developed by Vasomune Therapeutics, Inc. under a co-development agreement with AnGes, Inc. [TYO: 4563]. AV-001 is a novel investigational medicine that targets the Tie2 receptor, a transmembrane protein most highly expressed on the surface of endothelial cells in the vasculature. AV-001 activates the nonredundant Tie2-Angiopoietin signaling axis, and through stimulation of multiple downstream pathways normalizes the vasculature by enhancing endothelial cell stability, restoring normal barrier defense, and blocking vascular leak. Vascular dysfunction contributes to the underlying disease pathophysiology in patients with bacterial and viral acute respiratory distress syndrome, sepsis, hemorrhagic shock, acute kidney injury, stroke, and vascular dementia. Importantly, in multiple pre-clinical studies AV-001 tightened endothelial cell-cell junctions and promoted endothelial cell survival, which reduced pulmonary edema, and improved lung function compared to untreated controls translating into significantly improved survival. About Vasomune Therapeutics, Inc. Vasomune Therapeutics, Inc. is a private clinical-stage biopharmaceutical company developing the next generation of medicines to harness the body’s ability to defend against illness. Founded in 2014, Vasomune has focused on vascular normalization strategies, and has progressed the lead candidate AV-001 from bench to bedside. Vascular dysfunction is associated with the pathology of several disease states, including bacterial and viral acute respiratory distress syndrome, sepsis, hemorrhagic shock, acute kidney injury, stroke, and vascular dementia. Vasomune’s corporate headquarters and laboratories are in Toronto, Canada with US offices in Raleigh, NC. For more information about the company please visit . About AnGes, Inc. AnGes, Inc., a biopharmaceutical company founded in December 1999, focuses on the development of gene-based medicines. In March 2019, AnGes obtained conditional and time-limited approval for its lead product, Collategene® (Hepatocyte Growth Factor; HGF—plasmid gene therapy), for the treatment of lower limb ischemic ulcers. In September 2019, AnGes commenced commercialization in Japan of Collategene®, the world’s first marketed drug using plasmid DNA. AnGes is currently working on the development of a Tie2 tyrosine kinase receptor agonist (AV-001) for COVID-19, viral and bacterial-associated pneumonia and an NF-κB decoy oligonucleotide for chronic discogenic lumbar back pain. Furthermore, AnGes acquired EmendoBio in December 2020 to expand its capabilities in genome-editing technologies. For more information, visit .