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Quantum Biopharma Announces Completion of Dosing in 180-Day Repeated Dose Oral Toxicity and Toxicokinetic Studies for Lucid-21-302 (Lucid-MS)

Quantum Biopharma Ltd. - Class B Subordinate Voting Shares (QNTM) 
Company Research Source: GlobeNewswire
TORONTO, Dec. 23, 2025 (GLOBE NEWSWIRE) -- Quantum BioPharma Ltd. (NASDAQ: QNTM) (CSE: QNTM) (FRA: 0K91) (Upstream: QNTM) (“Quantum BioPharma” or the “Company”), a biopharmaceutical company dedicated to building a portfolio of innovative assets and biotech solutions for the treatment of challenging neurodegenerative and metabolic disorders and alcohol misuse disorders with drug candidates in different stages of development, today announces that oral dosing of Lucid-21-302 (Lucid-MS) is complete in both the 180-day toxicity and toxicokinetic studies. These studies will support the Investigational New Drug (IND) application with the US FDA, including the design of a Phase 2 trial of Lucid-MS in people with multiple sclerosis (MS). “We are very pleased that dosing is now complete in both 180-day chronic toxicity studies. These studies allow us to advance the Lucid-MS drug development program as they are critical components to the IND application with the FDA”, said Dr. Andrzej Chrusci Show less Read more
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