Updated LuMIERE Phase 1 data demonstrated a manageable safety profile with some preliminary evidence of anti-tumor activity
Eleven patients treated to date with 177Lu-FAP-2286 up to 7.4 GBq/dose
No serious adverse events, treatment discontinuations, or deaths related to 177Lu-FAP-2286 observed
Confirmed partial response (PR) in one patient who completed the maximum six administrations of 177Lu-FAP-2286 in the 3.7 GBq dose cohort
Patient continues without disease progression or subsequent anti-cancer therapy more than twelve months after first dose
Stable disease (SD) in one heavily pretreated patient who completed four administrations of 177Lu-FAP-2286 in the 5.55 GBq dose cohort
Recruitment of the 7.4 GBq dose cohort is ongoing
FAP-2286 has shown high tumor uptake and good prolonged retention across a range of solid tumors
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