We have successfully dosed the first of three patients in Cohort 8, the last cohort of the dose-ranging study in uMGMT #Glioblastoma Multiforme patients. The second patient has been enrolled and the treatment is planned. • Thus far, the preliminary data indicate no dose-limiting toxicities related to Temferon have been detected in any of 22 treated patients. • Temferon-derived differentiated cells were evident within the peripheral blood 14 days after infusion and were still detectable at more than 24 months. • As of December 2023, preliminary data in uMGMT patients, the most aggressive form of GBM, show a 2-year Overall Survival (OS) of 25%; the historically reported data observed in uMGMT and methilated patients undergoing current standard of care is approximately 14% to 18%, respectively. Dr. Luigi Naldini, stated, “Several techniques, including RNA single-cell analysis, suggest that Temferon can reprogram the Tumor Microenvironment in patients similarly to what we had demonstrated in preclinical models and activate the immune cell infiltration towards mounting immune responses against the tumor.” Genenta Science (Nasdaq $GNTA)
Incredibly Important Research...
Congratulations on your major accomplishment! You've earned it.
Genenta is truly a guiding light for the Italian research and tech transfer! Congrats! Well deserved!
Awesome news!
Very interesting approach to tame the TME! Hope the good works pays out to patients
Congrats Pierluigi Paracchi !!
Account Manager @ Worldwide Clinical Trials | Clinical Trial Development
8moCongratulations to everyone at Genenta!