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Australian Public Assessment Reports (AusPAR)

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An AusPAR provides information about the evaluation of a prescription medicine and the considerations that led the TGA to approve or not approve an application.

For more information see Australian Public Assessment Reports for prescription medicines (AusPARs).

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1062 result(s) found, displaying 1 to 25
  • Vaxchora (vibrio cholerae) vaccine has been approved for active immunisation against disease caused by Vibrio cholerae serogroup O1 in adults and children aged 2 years and older travelling to cholera-affected countries.
  • Vyalev (foslevodopa and foscarbidopa) has been approved to treat idiopathic Parkinson’s disease with severe motor fluctuations despite optimised alternative pharmacological treatment.
  • Jubbonti, a biosimilar to Prolia, and Wyost, a biosimilar to Xgeva (both denosumab), have been approved to improve bone density and to reduce bone fracture risk as a consequence of disease or medications that weaken bones.
  • Ebglyss (lebrikizumab) has been approved to treat severe atopic dermatitis in adult and adolescent patients.
  • Nubeqa has been approved to treat metastatic hormone-sensitive prostate cancer in combination with docetaxel.
  • Mounjaro (tirzepatide) has been approved, as an adjunct to a reduced-calorie diet and increased physical activity, for chronic weight management.
  • Kyprolis (carfilzomib) has been approved to treat relapsed or refractory multiple myeloma.
  • COMIRNATY Original/Omicron BA.4-5 Vaccine has been provisionally approved for immunisation against coronavirus disease 2019 (COVID-19) caused by SARSCoV-2 in individuals 6 months of age or older.
  • Amvuttra (vutrisiran) has been approved for the treatment of hereditary transthyretin-mediated amyloidosis in adult patients with polyneuropathy.
  • Velsipity (Etrasimod) has been approved for the treatment of adults with moderately to severely active ulcerative colitis who have not benefited from prior therapies
  • Opdivo (nivolumab), in combination with platinum-doublet chemotherapy, has been approved for the neoadjuvant treatment of patients with resectable non-small cell lung cancer.
  • Lokelma (sodium zirconium cyclosilicate hydrate) has been approved for the treatment of hyperkalaemia in adult patients.
  • Polivy (Polatuzumab vedotin) has been approved for the treatment of adult patients with previously untreated diffuse large B-cell lymphoma.
  • Enhertu (trastuzumab deruxtecan) has been approved to treat adult patients with unresectable or metastatic HER2-low breast cancer.
  • Onakta (tirbanibulin) was approved for the topical field treatment of actinic keratosis of the face or scalp in adults.
  • Wegovy has been approved for weight management in obese adolescents ages 12 years and above (as an adjunct to a reduced-calorie diet and increased physical activity).
  • Wegovy (semaglutide)has been approved as an adjunct to a reduced-energy diet and increased physical activity for chronic weight management (including weight loss and weight maintenance) in adults.
  • Xeljanz (tofacitinib) has been approved for the treatment of ankylosing spondylitis and for active polyarticular course juvenile idiopathic arthritis.
  • Rinvoq (upadacitinib) has been approved for the treatment of adults with active non-radiographic axial spondyloarthritis.
  • Nelarabine-Reach has been approved to treat patients with relapsing /refractory T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma.
  • Xenpozyme (olipudase alfa) has been approved as an enzyme replacement therapy for the treatment of noncentral nervous system manifestations of acid sphingomyelinase deficiency in paediatric and adult patients with Niemann-Pick disease (types A/B or B).
  • Winlevi (clascoterone) cream has been approved to treat acne vulgaris in patients 12 years of age or older.
  • Sohonos (palovarotene) has been approved to treat heterotopic ossification in individuals with fibrodysplasia ossificans progressiva.
  • Sidapvia (dapagliflozin+sitagliptin), a new drug combination, has been approved to treat type 2 diabetes mellitus in adults, as an adjunct to diet and exercise to improve glycaemic control.
  • Radicava (edaravone) was approved to treat adults with a diagnosis of amyotrophic lateral sclerosis who are independent in activities of daily living with normal respiratory function and where treatment is initiated within two years of disease onset.

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