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PAS-004 in Patients With Advanced Solid Tumors

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NCT06299839

Sponsored by Pasithea Therapeutics Corp. (industry) · KTTA — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
48estimated
Sites
7
Countries
Bulgaria, Romania, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-02-29actualWhen the study began enrolling
Primary completionFeb 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionFeb 2027estimatedThe whole study's end, after follow-up
First posted2024-03-08actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-12-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • RAS Mutation
  • NF1 Mutation
  • RAF Mutation
  • Advanced Solid Tumors

Interventions

  • Drug: PAS-004 Capsules
  • Drug: PAS-004 Tablets

Primary outcomes

what the primary-completion date above is the date OF
Evaluation of dose limiting toxicities (DLTs)
measured Day 1 through Day 35 (Cycle 1)
Evaluation of adverse events (AEs)
measured Screening through Day 1 through Day 35 (Cycle 1), and 30 days after discontinuation of study drug
Evaluation of AEs leading to discontinuation of investigational product (IP), PAS-004.
measured Screening through Day 1 through Day 35 (Cycle 1), and 30 days after discontinuation of study drug
Evaluation of hematology laboratory parameters
measured Screening through Day 1 through Day 35 (Cycle 1), and 30 days after discontinuation of study drug
Evaluation of clinical chemistry laboratory parameters
measured Screening through Day 1 through Day 35 (Cycle 1), and 30 days after discontinuation of study drug

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