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news
newsA few days ago, the American biotechnology company Fate announced the results of phase I clinical dose climbing of its induced pluripotent stem cell (iPSC) modified NK cell therapy FT516 and CAR-NK therapy FT596
.
Eight of 11 lymphoma patients responded with different doses of FT516, and six of them were CR
Drug source analysis
Drug source analysisThis result is quite good, roughly the same as the allogeneic CAR-T.
One of the main reasons for Fate's decline is its 9 billion market value
.
Previously, Fate only announced the data of 4 clinical patients, but because activated NK and CAR-NK are new treatments, investors have been full of strings and gave the most optimistic valuation
Unlike CAR-T, which relies on T cells, Fate's technology uses NK cells from the natural immune system
.
Fate's NK cells do not come from patients or healthy donors, but through iPSC differentiation technology
Only two of the four so-called highly malignant patients who are resistant to CAR-T have responded, which makes investors worry that CAR-NK does not have much advantage over allogeneic CAR-T in terms of efficacy
.
Although FT516 is not a CAR-NK, it has a similar structure.
Although CAR-T has a higher response rate in certain hematological tumors, durability and safety are issues that need to be resolved
.
Cell therapies similarly designed using other immune cells such as CAR-NK and CAR-M (macrophages) have recently begun to enter the clinic