Core Insights - AIM ImmunoTech Inc. is focusing on advancing clinical trials of Ampligen® for pancreatic cancer treatment, aiming for drug approval [2][4] - The company reported a bolstered cash position, with funding expected to last approximately 12 months following a public equity offering that raised $8.0 million [10] - Positive mid-year data from the Phase 2 clinical study of Ampligen® in combination with AstraZeneca's Imfinzi® shows no significant toxicity and superior progression-free survival (PFS) and overall survival (OS) [2][10] Financial Highlights - AIM ImmunoTech closed a public equity offering, raising $8.0 million in gross proceeds [10] - The company has regained its listing status on the NYSE American [10] Clinical Development - The ongoing Phase 2 study (DURIPANC) evaluates Ampligen® combined with Imfinzi® for metastatic pancreatic cancer patients with stable disease post-FOLFIRINOX [10] - The company has received U.S. and EU Orphan Drug designations for pancreatic cancer [10] Intellectual Property - AIM ImmunoTech has been granted U.S. patents covering methods of manufacturing therapeutic dsRNA, including Ampligen, and for its combination with PD-L1 drugs for cancer treatment [10] Company Overview - AIM ImmunoTech Inc. is an immuno-pharma company focused on developing therapeutics for various cancers, immune disorders, and viral diseases, with Ampligen® as its lead product [7]

Core Insights - AIM ImmunoTech Inc. reported positive mid-year data from the Phase 2 DURIPANC study, indicating promising signs of no significant toxicity and superior progression-free survival (PFS) and overall survival (OS) in metastatic pancreatic cancer patients treated with Ampligen® and durvalumab [1][3][5] Company Overview - AIM ImmunoTech is focused on developing therapeutics for various cancers, immune disorders, and viral diseases, with Ampligen® being its lead investigational drug [9] Study Details - The DURIPANC study is a collaboration with AstraZeneca and Erasmus Medical Center, aiming to evaluate the combination therapy of Ampligen and durvalumab in patients with stable disease post-FOLFIRINOX [1][4] - The study is expected to enroll up to 25 subjects, with 14 subjects enrolled as of the mid-year report [1] Preliminary Findings - The combination therapy has shown a well-tolerated safety profile, with approximately 21% of patients experiencing PFS greater than 6 months and 64% of eligible patients having OS greater than 6 months [5] - The study aims to assess clinical benefit rates, OS, PFS, and initiate immune-monitoring using tissue biopsies and immune profiling [1][2] Future Directions - Further analysis of immune-monitoring data is anticipated to provide insights into the biological activity and durability of response, as well as identify predictive biomarkers for patient selection [2][3] - The company has developed an intellectual property plan, including a U.S. patent for Ampligen as an oncology treatment, extending protection to August 9, 2039 [8]