Pasithea Therapeutics Announces Initiation of Phase 1/1B Study of PAS-004 in Adult NF1 Patients and Activation of First Clinical Trial Site

-- First patient expected to be dosed during Q2 2025 --
-- Trial will evaluate safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy in both plexiform neurofibromas and cutaneous neurofibromas --
-- Starting dose of 4mg tablet QD (once daily) --
-- First trial site in Australia. Four additional sites planned for Australia, South Korea, and U.S. –
-- Australian R&D Tax Incentive refund of up to 48.5% of eligible study-related costs expected --

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