Akeso, Inc. ((HK:9926)) announced an update on their ongoing clinical study.
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Akeso, Inc. (HK:9926) has announced a new clinical study titled ‘An Exploratory Study to Evaluate Safety and Efficacy of the Neoantigen Personalized mRNA Vaccine AK154 Monotherapy or in Combination With AK104 or AK112, and the Sequential mFOLFIRINOX Regimen as Adjuvant Therapy in Surgically Resectable Pancreatic Ductal Adenocarcinoma.’ The study aims to assess the safety and efficacy of personalized mRNA vaccines in treating pancreatic ductal adenocarcinoma (PDAC), a significant advancement in cancer treatment.
The study is testing several interventions, including the biological agents AK154, Cadonilimab, and Ivonescimab, alongside the drug regimen mFOLFIRINOX. AK154 is a neoantigen personalized mRNA vaccine, Cadonilimab is a PD-1/CTLA-4 bispecific antibody, and Ivonescimab is a PD-1/VEGF bi-specific antibody. The mFOLFIRINOX regimen consists of Fluorouracil, leucovorin, Irinotecan, and Oxaliplatin.
This interventional study is designed as a Phase 1 trial with a sequential intervention model and no masking, focusing primarily on treatment. The study is not yet recruiting participants, indicating it is in the early stages of implementation.
The study was first submitted on March 30, 2025, with the same date marking its last update. These dates are crucial as they indicate the study’s timeline and readiness to progress to participant recruitment.
The market implications of this study are significant for Akeso, Inc., as successful outcomes could enhance their stock performance and investor confidence. The study’s focus on innovative mRNA vaccine therapies positions Akeso at the forefront of cancer treatment advancements, potentially impacting the competitive landscape in the biotechnology sector.
The study is ongoing, with further details available on the ClinicalTrials portal.
