AIM ImmunoTech Announces First Dose Level is Generally Well-Tolerated in Phase 1b/2 Study of Ampligen and Imfinzi as a Combination Therapy for Late-Stage Pancreatic Cancer
AIM ImmunoTech Inc. (AIM)
Company Research
Source: GlobeNewswire
OCALA, Fla., April 29, 2024 (GLOBE NEWSWIRE) -- AIM ImmunoTech Inc. (NYSE American: AIM) (“AIM” or the “Company”) today announced that it has taken an essential step forward in testing the combination of AIM’s Ampligen® (rintatolimod) and AstraZeneca’s anti-PD-L1 immune checkpoint inhibitor Imfinzi® (durvalumab) in the treatment of late-stage pancreatic cancer (the “DURIPANC” study). See: ClinicalTrials.gov NCT05927142. Investigators at Erasmus Medical Center ("Erasmus MC") in the Netherlands have completed the safety evaluation of patients enrolled in the first dose level of the dose escalation design in the Phase 1b/2 study. The combination of Ampligen and Imfinzi was found to be generally well-tolerated with no severe adverse events (“SAE”) or dose-limiting toxicities (“DLT”). Based on these positive results, escalation to the next dose will occur according to protocol design and AIM expects the next cohort of patients to begin dosing very soon. Subjects will be in trea
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News
- AIM ImmunoTech Reports First Quarter 2024 Financial Results and Provides Corporate Update [Yahoo! Finance]Yahoo! Finance
- AIM ImmunoTech Reports First Quarter 2024 Financial Results and Provides Corporate UpdateGlobeNewswire
- AIM ImmunoTech to Discuss First Quarter 2024 Financial Results on May 16, 2024, and Host Conference Call and WebcastGlobeNewswire
- AIM ImmunoTech Completes cGMP Manufacturing of Clinical Vials of Ampligen® [Yahoo! Finance]Yahoo! Finance
- AIM ImmunoTech Completes cGMP Manufacturing of Clinical Vials of Ampligen®GlobeNewswire
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Sec Filings
- 5/15/24 - Form 10-Q
- 5/7/24 - Form 4
- 5/7/24 - Form 4
- AIM's page on the SEC website