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Grafa

Clearmind Medicine hits primary safety endpoint in Phase I/IIa alcohol use disorder trial

Clearmind Medicine (NASDAQ:CMND), a clinical-stage pharmaceutical company focused on developing novel psychedelic-derived therapies, announced today that its lead candidate, CMND-100, has successfully met the primary safety and tolerability endpoints in its Phase I/IIa clinical trial.

Read more: Clearmind Medicine hits primary safety endpoint in Phase I/IIa alcohol use disorder trial
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Genprex preclinical data shows Reqorsa overcoming resistance in lung cancer

Genprex (NASDAQ:GNPX), a clinical-stage gene therapy company, announced today that its collaborators presented compelling preclinical data for its lead drug candidate, Reqorsa® (quaratusugene ozeplasmid), at the American Association for Cancer Research (AACR) Annual Meeting 2026.

Read more: Genprex preclinical data shows Reqorsa overcoming resistance in lung cancer
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Industrials

Stanley Black & Decker affirms 2026 outlook following Section 232 tariff updates

Stanley Black & Decker (NYSE:SWK) announced today that recent adjustments to the Section 232 tariff regime—the federal trade policy governing aluminum and steel imports—are not expected to have a material impact on the company’s full-year 2026 financial guidance.

Read more: Stanley Black & Decker affirms 2026 outlook following Section 232 tariff updates
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Nanobiotix Nanoprimer enhances LNP-DNA delivery, reduces liver toxicity in preclinical trials

Nanobiotix (NASDAQ:NBTX), a late-clinical stage biotechnology company, announced the presentation of new preclinical data today at the 2026 Annual Meeting of the American Association for Cancer Research (AACR).

Read more: Nanobiotix Nanoprimer enhances LNP-DNA delivery, reduces liver toxicity in preclinical trials
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Medicus Pharma seeks FDA orphan drug status for novel microneedle skin cancer therapy

Medicus Pharma (NASDAQ:MDCX), a clinical-stage biopharmaceutical company, announced today that it has submitted an application for Orphan Drug Designation (ODD) to the U.S. Food and Drug Administration (FDA) for its flagship candidate, SkinJect (D-MNA).

Read more: Medicus Pharma seeks FDA orphan drug status for novel microneedle skin cancer therapy