Pasithea Therapeutics Announces Completion of Enrollment and Initial Dosing of Cohort 2 following Positive Safety Review Committee (SRC) Recommendation for PAS-004 in Ongoing Phase 1 Clinical Trial

June 13, 2024

https://www.globenewswire.com/news-release/2024/06/13/2898133/0/en/Pasithea-Therapeutics-Announces-Completion-of-Enrollment-and-Initial-Dosing-of-Cohort-2-following-Positive-Safety-Review-Committee-SRC-Recommendation-for-PAS-004-in-Ongoing-Phase-1.html

MIAMI, June 13, 2024 (GLOBE NEWSWIRE) — Pasithea Therapeutics Corp. (NASDAQ:KTTA) (“Pasithea” or the “Company”), a clinical-stage biotechnology company developing PAS-004, a next-generation macrocyclic MEK inhibitor, for the treatment of neurofibromatosis type 1 (NF1) and other indications, announced today that an independent Safety Review Committee (SRC) has completed its safety review of data from the first dose cohort (2mg) treated in the ongoing Phase 1 clinical trial (NCT06299839) of PAS-004 in patients with MAPK pathway driven advanced solid tumors with a documented RAS, NF1 or RAF mutation or patients who have failed BRAF/MEK inhibition.

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