Pasithea Therapeutics Corporation announced updates on its clinical development programs for PAS-004, a next-generation oral macrocyclic MEK inhibitor. The company has completed enrollment of 12 patients in the first four dose cohorts of its Phase 1/1b clinical trial (NCT06961565) in adult patients with neurofibromatosis type 1 associated plexiform neurofibromas (NF1-PN). Pasithea plans to present safety, tolerability, pharmacokinetic, and efficacy data, including six-month outcomes for both plexiform and cutaneous neurofibromas, in the second half of 2026. Additionally, in its ongoing Phase 1 clinical trial in advanced cancer patients (NCT06299839), Pasithea expects to present longer-term follow-up data from Cohorts 4 through 8 in the second quarter of 2026. Results from these studies have not yet been presented and will be released in the future according to the company’s outlined timelines.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Pasithea Therapeutics Corporation published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9624463) on January 13, 2026, and is solely responsible for the information contained therein.
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