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21 result(s) found, displaying 1 to 10
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for TEVIMBRA tislelizumab 100 mg/10 mL concentrated injection vial.
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Australian Public Assessment Report (AusPAR)BRUKINSA (zanubritinib) was approved to treat adult patients with chronic lymphocytic leukaemia or small lymphocytic lymphoma, including patients with deletion 17p and/or TP53 mutation.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for TEVIMBRA tislelizumab 100 mg/10 mL concentrated injection vial.
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Australian Public Assessment Report (AusPAR)Tevimbra (tislelizumab) has been approved for the treatment of oesophageal squamous cell carcinoma and non-small cell lung cancer.
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Prescription medicine decision summaryTevimbra (tislelizumab) has been approved for the treatment of patients with various types of oesophageal squamous cell carcinoma and non-small cell lung cancer.
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Jul-2024Prescription medicine evaluationActive ingredient: tislelizumab.
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Apr-2024Prescription medicine evaluationActive ingredient: tislelizumab.
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Oct-2023Prescription medicine evaluationActive ingredient: tislelizumab.