Patients (n=3) in this third dose level received a total dose of 240 X 106 CHM 1101 (CLTX CAR T)
cells through dual routes of intratumoral and intraventricular administration.
Once the final evaluable patient of this third dose cohort successfully completes the 28 DLT
period, the study will be able to advance to recruitment of patients at the fourth and final
planned dose level of 440 X 106 CHM 1101 (CLTX CAR T) cells through dual routes of
administration (intratumoral and intracranial intraventricular).
It is a lengthy process but the Team is moving forward as fast as possible. Safety is no problem it seems, focus is now on early signs of efficacy.
What an opportunity to grab shares sub 8c from those who can't or aren't able to wait a bit longer.
Well done Team CHM.
GLTA
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