Sunday, June 22, 2025 9:37:39 PM
Meirluc, Agree. I did an AI search and here's what I found as clinical data support poly-ICLC's safety and potential efficacy in GBM, other than the UCLA phase 2 trial:
Phase II trials demonstrated improved survival when combined with radiotherapy and temozolomide in newly diagnosed GBM, with median overall survival of 18.3 months vs. 14.6 months in controls. 2010
https://pmc.ncbi.nlm.nih.gov/articles/PMC3018929/
Pediatric trials reported stable disease in low-grade glioma patients and manageable toxicity (e.g., transient fever, mild injection-site reactions). 2015
https://pmc.ncbi.nlm.nih.gov/articles/PMC4356196/
Preclinical and clinical evidence suggests synergy with vaccines and immune checkpoint inhibitors by enhancing dendritic cell maturation and T-cell activation. 2021
https://pmc.ncbi.nlm.nih.gov/articles/PMC8229304/
In the United States, oncologists may prescribe FDA-approved drugs for off-label uses under their medical discretion, provided the decision is evidence-based and prioritizes patient safety.
Phase II trials demonstrated improved survival when combined with radiotherapy and temozolomide in newly diagnosed GBM, with median overall survival of 18.3 months vs. 14.6 months in controls. 2010
https://pmc.ncbi.nlm.nih.gov/articles/PMC3018929/
Pediatric trials reported stable disease in low-grade glioma patients and manageable toxicity (e.g., transient fever, mild injection-site reactions). 2015
https://pmc.ncbi.nlm.nih.gov/articles/PMC4356196/
Preclinical and clinical evidence suggests synergy with vaccines and immune checkpoint inhibitors by enhancing dendritic cell maturation and T-cell activation. 2021
https://pmc.ncbi.nlm.nih.gov/articles/PMC8229304/
In the United States, oncologists may prescribe FDA-approved drugs for off-label uses under their medical discretion, provided the decision is evidence-based and prioritizes patient safety.
Sharing thoughts and opinions. To participate in group due diligence. Motto: Do not be a gullible FUDdable investor.
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