WO2025022354 - TREATMENT OF LOW-GRADE INTERMEDIATE-RISK NON-MUSCLE INVASIVE BLADDER CANCER WITH A THERMALLY GELLING PHARMACEUTICAL COMPOSITION CONTAINING MITOMYCIN

National phase entry:
Publication Number WO/2025/022354
Publication Date 30.01.2025
International Application No. PCT/IB2024/057229
International Filing Date 25.07.2024
Title **
[English] TREATMENT OF LOW-GRADE INTERMEDIATE-RISK NON-MUSCLE INVASIVE BLADDER CANCER WITH A THERMALLY GELLING PHARMACEUTICAL COMPOSITION CONTAINING MITOMYCIN
[French] TRAITEMENT DU CANCER DE LA VESSIE INVASIF NON MUSCULAIRE À RISQUE INTERMÉDIAIRE DE FAIBLE QUALITÉ AVEC UNE COMPOSITION PHARMACEUTIQUE THERMOGÉLIFIANTE CONTENANT DE LA MITOMYCINE
Applicants **
UROGEN PHARMA LTD.
Inventors
RAJU, Sunil
Priority Data
63/515,352   25.07.2023   US
63/640,252   30.04.2024   US
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting2297
EPO Filing, Examination, Granting9294
Japan Filing, Examination, Granting2062
South Korea Filing, Examination, Granting1916
USA Filing, Examination, Granting4740
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Total: 20,309

The term for entry into the National Phase has expired. This quotation is for informational purposes only

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Abstract[English] A method of reducing risk of bladder tumor recurrence, progression or death, or a method of increasing probability of disease-free survival at 15 months post-treatment, or a method of increasing probability of maintaining an achieved complete response for at least 15 months post-treatment comprises administering to a patient in need thereof a thermally gelling pharmaceutical composition once weekly for six weeks, the patient having low-grade intermediate-risk non-muscle invasive bladder cancer, and the thermally gelling pharmaceutical composition comprising a reverse thermal gelation agent, a polymer, and mitomycin. The risk is reduced or the probability is increased in comparison to the risk or probability expected if the patient were instead to receive TURBT monotherapy as treatment.[French] Un procédé de réduction du risque de récidive, de progression ou de mort de tumeur de la vessie, ou un procédé d'augmentation de la probabilité de survie sans maladie à 15 mois après traitement, ou un procédé d'augmentation de la probabilité de maintien d'une réponse complète atteinte pendant au moins 15 mois après traitement comprend l'administration à un patient qui en a besoin d'une composition pharmaceutique thermogélifiante une fois hebdomadaire pendant six semaines, le patient ayant un cancer de la vessie invasif non musculaire à risque intermédiaire de faible qualité, et la composition pharmaceutique thermogélifiante comprenant un agent de gélification thermique inverse, un polymère et de la mitomycine. Le risque est réduit ou la probabilité est augmentée par rapport au risque ou à la probabilité attendu si le patient devait plutôt recevoir une monothérapie TURBT en tant que traitement.