Quantum BioPharma Announces Completion of Dosing in 90-Day Repeated Dose Oral Toxicity and Toxicokinetic Studies for Lucid-MS for Multiple Sclerosis
Quantum BioPharma (NASDAQ: QNTM) has completed the dosing phase of 90-day oral toxicity and toxicokinetic studies for its Multiple Sclerosis drug candidate Lucid-21-302 (Lucid-MS). These studies are crucial for supporting an upcoming Investigational New Drug (IND) application with the US FDA, which the company aims to submit by the end of 2025. The completion of these toxicity studies marks a significant step toward initiating a Phase 2 trial for Lucid-MS, which is being developed as a first-in-class treatment for Multiple Sclerosis patients.
Quantum BioPharma (NASDAQ: QNTM) ha completato la fase di somministrazione degli studi di tossicitĂ orale e tossicocinetica della durata di 90 giorni per il suo candidato farmaco per la Sclerosi Multipla, Lucid-21-302 (Lucid-MS). Questi studi sono fondamentali per supportare la prossima domanda di Nuovo Farmaco Sperimentale (IND) presso la FDA statunitense, che l'azienda prevede di presentare entro la fine del 2025. Il completamento di questi studi di tossicitĂ rappresenta un passo importante verso l'avvio di una fase 2 per Lucid-MS, sviluppato come trattamento innovativo per i pazienti con Sclerosi Multipla.
Quantum BioPharma (NASDAQ: QNTM) ha completado la fase de dosificaciĂłn de los estudios de toxicidad oral y toxicocinĂ©tica de 90 dĂas para su candidato a medicamento para Esclerosis MĂșltiple, Lucid-21-302 (Lucid-MS). Estos estudios son esenciales para respaldar una prĂłxima solicitud de Nuevo FĂĄrmaco en InvestigaciĂłn (IND) ante la FDA de EE. UU., que la compañĂa planea presentar antes de finales de 2025. La finalizaciĂłn de estos estudios de toxicidad representa un paso importante para iniciar un ensayo de Fase 2 para Lucid-MS, desarrollado como un tratamiento novedoso para pacientes con Esclerosis MĂșltiple.
Quantum BioPharma (NASDAQ: QNTM)ë� ë€ë°ì� êČœíìŠ� ìčëŁ í볎 ìœëŹŒì� Lucid-21-302 (Lucid-MS)ì� ëí� 90ì� êČœê”Ź ë ì± ë°� ë ì±ëíí� ì°ê”Źì� íŹìŹ ëšêłë„� ìëŁíì”ëë€. ì� ì°ê”Źë€ì ëŻžê” FDAì� ì ì¶í� ìì ì� ìììíì ìœ(IND) ì ìČì� ì§ìíë� ë� ë§€ì° ì€ìíë©°, íìŹë� 2025ë � ë§êčì§ ì ì¶íë êČì ëȘ©íëĄ� íêł ìì”ëë€. ì� ë ì± ì°ê”Źì� ìëŁë� ë€ë°ì� êČœíìŠ� íìë€ì ìí ì”ìŽì� íì ì � ìčëŁëČìŒëĄ� ê°ë° ì€ìž Lucid-MSì� 2ì� ìí ê°ìë„� í„í ì€ìí� ì§ì ì ëë�.
Quantum BioPharma (NASDAQ : QNTM) a achevé la phase d'administration des études de toxicité orale et toxicocinétique de 90 jours pour son candidat médicament contre la sclérose en plaques, Lucid-21-302 (Lucid-MS). Ces études sont essentielles pour appuyer une prochaine demande d'Investigational New Drug (IND) auprÚs de la FDA américaine, que la société prévoit de soumettre d'ici la fin de 2025. L'achÚvement de ces études de toxicité marque une étape importante vers le lancement d'un essai de phase 2 pour Lucid-MS, développé comme un traitement innovant pour les patients atteints de sclérose en plaques.
Quantum BioPharma (NASDAQ: QNTM) hat die Dosierungsphase der 90-tĂ€gigen oralen ToxizitĂ€ts- und Toxikokinetikstudien fĂŒr seinen Multiple-Sklerose-Wirkstoffkandidaten Lucid-21-302 (Lucid-MS) abgeschlossen. Diese Studien sind entscheidend zur UnterstĂŒtzung eines bevorstehenden Antrags auf ein Investigational New Drug (IND) bei der US-amerikanischen FDA, den das Unternehmen bis Ende 2025 einreichen möchte. Der Abschluss dieser ToxizitĂ€tsstudien stellt einen bedeutenden Schritt in Richtung Einleitung einer Phase-2-Studie fĂŒr Lucid-MS dar, das als neuartiges Erstbehandlungsmedikament fĂŒr Multiple-Sklerose-Patienten entwickelt wird.
- Successful completion of 90-day toxicity studies, advancing the drug development program
- Plans to submit IND application by end of 2025, showing clear regulatory pathway
- Advancing towards Phase 2 trials, indicating promising development progress
- Potential first-in-class treatment for Multiple Sclerosis, suggesting competitive advantage
- Still in pre-clinical stage, requiring significant development time before potential commercialization
- No efficacy data or trial results shared in the announcement
- IND approval not guaranteed, presenting regulatory risk
TORONTO, May 12, 2025 (GLOBE NEWSWIRE) -- Quantum BioPharma Ltd. (NASDAQ: QNTM) (CSE: QNTM) (FRA: 0K91) (â�Quantum BioPharmaâ� or the â�Companyâ�), a biopharmaceutical company dedicated to building a portfolio of innovative assets and biotech solutions, today announced that dosing of drug has completed in 90-day oral toxicity and toxicokinetic studies for Lucid-21-302 (Lucid-MS) for Multiple Sclerosis (âMSâ�). These studies were commissioned to provide data to support an IND application with the US FDA.
âWe are very pleased to have completed dosing in these toxicity studies as this advances the Lucid-21-302 drug development program,â� said Dr. Andrzej Chruscinski, Vice-President, Scientific and Clinical Affairs at Quantum Biopharma. âReports from these studies will support an IND application, which we hope to submit before the end of the year.â�
Zeeshan Saeed, CEO of Quantum BioPharma added, âWe are excited about potential of Lucid-21-302 as a new first-in-class treatment for Multiple Sclerosis. By completing these toxicity studies, we are now closer to initiating a Phase 2 trial of Lucid-21-302 in people with MS.â�
About Quantum BioPharma Ltd.
Quantum BioPharma (NASDAQ: QNTM) is 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. Through its wholly owned subsidiary, Lucid Psycheceuticals Inc. (â�Lucidâ�), Quantum BioPharma is focused on the research and development of its lead compound, Lucid-MS. Lucid-MS is a patented new chemical entity shown to prevent and reverse myelin degradation, the underlying mechanism of multiple sclerosis, in preclinical models. Quantum BioPharma invented unbuzzdâ� and spun out its OTC version to a company, Celly Nutrition Corp. (â�Celly Nutritionâ�), led by industry veterans. Quantum BioPharma retains ownership of
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Forward-Looking Information
This press release contains certain âforward-looking statementsâ� within the meaning of applicable Canadian securities law. Any statements that express or involve discussions with respect to predictions, expectations, beliefs, plans, projections, objectives, assumptions or future events or performance (often, but not always, identified by words or phrases such as âbelievesâ�, âanticipatesâ�, âexpectsâ�, âis expectedâ�, âscheduledâ�, âestimatesâ�, âpendingâ�, âintendsâ�, âplansâ�, âforecastsâ�, âtargetsâ�, or âhopesâ�, or variations of such words and phrases or statements that certain actions, events or results âmayâ�, âcouldâ�, âwouldâ�, âwillâ�, âshouldâ� âmightâ�, âwill be takenâ�, or âoccurâ� and similar expressions) are not statements of historical fact and may be forward-looking statements. The forward-looking information and forward-looking statements contained herein include, but are not limited to, statements regarding: the Companyâs focus on the research and development of Lucid-MS to prevent and reverse myelin degradation; the Companyâs Lucid-21-302 clinical development program in multiple sclerosis advancing towards human phase-2 efficacy trials; Lucid-21-302 having an initial indication in multiple sclerosis; the Companyâs intention to retain
Forward-looking information in this news release are based on certain assumptions and expected future events, namely: the Companyâs assessment of market conditions, its ability to gain market share, and its potential competitive edge are accurate; the Company will have the ability to carry out its plans with respect to its new innovation and offerings, including its ability to conduct research and development of Lucid-MS; the Companyâs Lucid-21-302 clinical development program in multiple sclerosis will advance towards human phase-2 efficacy trials; Lucid-21-302 having an initial indication in multiple sclerosis; the Company will retain
These statements involve known and unknown risks, uncertainties and other factors, which may cause actual results, performance or achievements to differ materially from those expressed or implied by such statements, including but not limited to: the Companyâs inability to retain
The reader is urged to refer to additional information relating to Quantum BioPharma, including its annual information form, can be located on the SEDAR+ website at www.sedarplus.ca and on the EDGAR section of the United States Securities and Exchange Commissionâs website at for a more complete discussion of such risk factors and their potential effects.
Contacts:
Quantum BioPharma Ltd.
Zeeshan Saeed, Founder, CEO and Executive Co-Chairman of the Board
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Telephone: (833) 571-1811
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