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11 result(s) found, displaying 1 to 10
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Australian Public Assessment Report (AusPAR)Amvuttra (vutrisiran) has been approved for the treatment of hereditary transthyretin-mediated amyloidosis in adult patients with polyneuropathy.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for OXLUMO lumasiran (as sodium) 94.5 mg/0.5 mL injection vial.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for AMVUTTRA, vutrisiran (as sodium) 25 mg / 0.5 mL solution for injection pre-filled syringe.
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Prescription medicine decision summaryAmvuttra (vutrisiran) was approved for the treatment of hereditary transthyretin-mediated amyloidosis in adult patients with stage 1 or stage 2 polyneuropathy.
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Australian Public Assessment Report (AusPAR)Givlaari (givosiran sodium) has been approved for the treatment of acute hepatic porphyria.
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Prescription medicine registrationActive ingredients: lumasiran sodium.
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Prescription medicine registrationActive ingredients: vutrisiran sodium.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for GIVLAARI givosiran 189 mg/1mL solution for injection vial.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for ONPATTRO patisiran 10 mg/5 mL concentrated injection for infusion vial.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for KIMMTRAK tebentafusp 0.1 mg/0.5 mL concentrated solution for infusion vial.