Pasithea Therapeutics Announces FDA Acceptance of IND Application to Evaluate PAS-004 in Advanced Cancer Patients

January 2, 2024

https://www.globenewswire.com/news-release/2024/01/02/2802677/0/en/Pasithea-Therapeutics-Announces-FDA-Acceptance-of-IND-Application-to-Evaluate-PAS-004-in-Advanced-Cancer-Patients.html

— PAS-004 is the first macrocyclic MEK inhibitor to enter human clinical trials —

— Phase 1 dose escalation study in patients with MAPK pathway driven advanced solid tumors to begin in Q1 2024 –

Read more at globenewswire.com

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