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Presented for research literature review only Choi JW et al
Therefore, therapeutic approaches may need to be more nuanced, perhaps targeting specific drivers of pathological senescence, modulating the harmful components of the SASP (senomorphics), or selectively targeting only the chronically persistent senescent cells
A clinical study report will be submitted to the US FDA and results will be available on www.clinicaltrials.gov within 12 months of completion of the study
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