$KTTA

Pasithea Therapeutics Corp.

Insider trades

No enriched coverage for $KTTA in the last 7 days.

No SEC Form 4 filings for $KTTA in the last 30 days.

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Pasithea's PAS-004 Receives FDA Orphan Drug Designation In Treating AL. Sclerosis

Pasithea Therapeutics (KTTA) said the U.S. FDA granted Orphan Drug Designation to PAS-004 for amyotrophic lateral sclerosis (ALS). The company said PAS-004 is a macrocyclic MEK inhibitor and is in Phase 1 trials in advanced cancer and Phase 1/1b trials in NF1-associated plexiform neurofibromas. Orphan status can bring tax credits, fee exemptions, and up to seven years’ exclusivity after approval.

KTTA SEC Filings - Pasithea Therapeutics Corp 10-K, 10-Q, 8-K Forms

This page provides a comprehensive resource for investors and traders to access Pasithea Therapeutics (KTTA) SEC filings, including annual, quarterly, and material event reports, alongside insider trading forms. Each filing is accompanied by an AI-generated summary, sentiment and impact scores, and end-of-day stock performance data. The platform aims to simplify access to critical regulatory disclosures with analytical insights and historical market reactions.

KTTA sentiment & insider activity

Recent KTTA coverage spans financial news, insider activity and regulation.

What's driving KTTA

  • A 10% owner’s indirect open-market purchase is a modest, sentiment-relevant signal but not a fundamental catalyst by itself.

    SEC EDGAR · Jun 22, 2026

  • Orphan designation improves regulatory and commercial optionality for PAS-004 in ALS, potentially strengthening investor expectations for future trial/approval pathways.

    rttnews.com · Jun 2, 2026

  • Pasithea Therapeutics (KTTA) has released its SEC filings, including annual, quarterly, and material event reports. The filings indicate ongoing clinical development and financial stability, with a somewhat bullish sentiment from recent market reactions.

    Stock Titan · Apr 1, 2026

  • The $60 million public offering by Pasithea Therapeutics (KTTA) is likely to cause short-term stock dilution but may provide capital for growth initiatives. The market reaction appears neutral, with limited immediate impact on stock price.

    GlobeNewswire · Nov 28, 2025

  • Recent positive updates on KTTA's lead drug candidate and a new grant have led to a sharp rise in stock price, indicating bullish sentiment. The news suggests potential short-term upward movement, but underlying fundamentals and market conditions should be considered for sustained gains.

    Benzinga · Nov 26, 2025

alphai scores every news story that mentions KTTA with an AI model for sentiment and relevance, and aggregates insider trades from Pasithea Therapeutics Corp.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $KTTA

Score
$KTTAMedAI 9/10

Pasithea's PAS-004 Receives FDA Orphan Drug Designation In Treating AL. Sclerosis

Pasithea Therapeutics (KTTA) said the U.S. FDA granted Orphan Drug Designation to PAS-004 for amyotrophic lateral sclerosis (ALS). The company said PAS-004 is a macrocyclic MEK inhibitor and is in Phase 1 trials in advanced cancer and Phase 1/1b trials in NF1-associated plexiform neurofibromas. Orphan status can bring tax credits, fee exemptions, and up to seven years’ exclusivity after approval.

$KTTALow

KTTA SEC Filings - Pasithea Therapeutics Corp 10-K, 10-Q, 8-K Forms

This page provides a comprehensive resource for investors and traders to access Pasithea Therapeutics (KTTA) SEC filings, including annual, quarterly, and material event reports, alongside insider trading forms. Each filing is accompanied by an AI-generated summary, sentiment and impact scores, and end-of-day stock performance data. The platform aims to simplify access to critical regulatory disclosures with analytical insights and historical market reactions.

$KTTAHigh

Pasithea Therapeutics Announces Positive Phase 1 Data Including Partial Response, Demonstrating Monotherapy Clinical Activity and Favorable Safety Profile for PAS-004 in Advanced Cancer Study - Pasithea Therapeutics (NASDAQ:KTTA), Pasithea Therapeutics (NASDAQ:KTTAW)

-- Evidence of Monotherapy Activity: Partial response observed in a MEK-rechallenge 3rd-line melanoma patient with BRAF V600E mutation who remains on trial for more than 11 months -- -- A second MEK-rechallenge 3rd-line melanoma patient with BRAF V600E mutation has achieved stable disease and ...

$KTTAMed

Pasithea Therapeutics Announces Enrollment of Cohort 2 following Positive Safety Review Committee (SRC) Recommendation for its Ongoing Phase 1/1b Clinical Trial of PAS-004 in Adult NF1 Patients - Pasithea Therapeutics (NASDAQ:KTTA), Pasithea Therapeutics (NASDAQ:KTTAW)

-- Recommendation that trial escalate to next dose level of 8mg tablet -- -- Initial interim clinical data from first two cohorts expected in Q1 2026 -- MIAMI, Sept. 08, 2025 ( GLOBE NEWSWIRE ) -- Pasithea Therapeutics Corp.

$KTTAMed

Pasithea Therapeutics Updates Time of Presentation at the H.C. Wainwright 27th Annual Global Investment Conference - Pasithea Therapeutics (NASDAQ:KTTA), Pasithea Therapeutics (NASDAQ:KTTAW)

MIAMI, Aug. 29, 2025 ( GLOBE NEWSWIRE ) -- Pasithea Therapeutics Corp. KTTA ( "Pasithea" or the "Company" ) , a clinical-stage biotechnology company developing PAS-004, a next-generation macrocyclic MEK inhibitor, today announced change of date and time of management's live presentation at the ...

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