🇺🇸 FDA
Pipeline program

A Phase 1 Open-label Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of PAS-004, a MEK (1/2) Inhibitor, 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

Phase 1 other active

Quick answer

A Phase 1 Open-label Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of PAS-004, a MEK (1/2) Inhibitor, 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 for Solid Tumors is a Phase 1 program (other) at Pasithea Therapeutics with 1 ClinicalTrials.gov record(s).

Program details

Company
Pasithea Therapeutics
Indication
Solid Tumors
Phase
Phase 1
Modality
other
Status
active

Clinical trials