Health Canada approves Iqirvo as a first-in-class dual-peroxisome proliferator-activated receptor treatment for primary biliary cholangitis

28 April 2025 - Iqirvo (elafibranor) is the first new medicine approved in nearly a decade for the treatment of ...

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Telix provides regulatory update on TLX101-CDx

28 April 2028 - Telix Pharmaceuticals today announces that it has received a complete response letter from the US FDA ...

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Lynozyfic (linvoseltamab) approved in the European Union for the treatment of relapsed/refractory multiple myeloma

28 April 2025 - Regeneron Pharmaceuticals today announced that the European Commission has granted conditional marketing approval of Lynozyfic (linvoseltamab) to ...

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Vertex receives CHMP positive opinion for Alyftrek, a new once-daily CFTR modulator for the treatment of cystic fibrosis

28 April 2025 - In head-to-head clinical trials, deutivacaftor/tezacaftor/vanzacaftor was non-inferior on ppFEV1 and superior compared to Kaftrio (ivacaftor/tezacaftor/elexacaftor) at ...

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Jazz Pharmaceuticals receives CHMP positive opinion for zanidatamab for the treatment of advanced HER2 positive biliary tract cancer

25 April 2025 - Jazz Pharmaceuticals today announced that the CHMP of the EMA has adopted a positive opinion recommending the ...

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New treatment against Duchenne muscular dystrophy

25 April 2025 - Duvyzat can be used in a wide patient population from the age of six. ...

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First treatment against severe thyroid eye disease

25 April 2025 - Tepezza significantly improves symptoms for patients with moderate to severe thyroid eye disease ...

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AbbVie submits biologics license application to US FDA for trenibotulinumtoxinE (TrenibotE) for the treatment of glabellar lines

24 April 2025 - Submission is supported by data from over 2,100 patients treated with TrenibotE throughout the clinical program. ...

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Tremfya (guselkumab) receives European Commission approval for adults with moderately to severely active ulcerative colitis, strengthening Johnson & Johnson’s leadership in inflammatory bowel disease

25 April 2025 - Johnson & Johnson today announced that the European Commission has approved a Marketing Authorisation for Tremfya (guselkumab) ...

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CHMP recommends approval of Oczyesa for treatment of acromegaly in the EU

25 April 2025 - Camurus today announced that the EMA's CHMP has adopted a positive opinion for market authorisation of Oczyesa, ...

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FDA approves penpulimab-kcqx for non-keratinizing nasopharyngeal carcinoma

23 April 2025 - Today, the FDA approved penpulimab-kcqx (Akeso Biopharma) with cisplatin or carboplatin and gemcitabine for the first-line ...

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Latest update on US FDA BLA for Novavax's COVID-19 vaccine

23 April 2025 - We believe that our biologics license application is approvable based on conversations with the US FDA, ...

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Sarclisa approved in Canada for patients with newly diagnosed multiple myeloma

22 April 2025 - This is the third indication for Sarclisa in Canada for the treatment of multiple myeloma. ...

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Health Canada approves Keytruda plus pemetrexed and platinum chemotherapy as first-line treatment for adult patients with unresectable advanced or metastatic malignant pleural mesothelioma

22 April 2025 - Approval is based on the results from the Phase 3 CCTG IND.227/KEYNOTE-483 trial. ...

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FDA grants breakthrough therapy designation for BrainChild Bio’s B7-H3 CAR T-cell therapy for incurable paediatric brain tumours

22 April 2025 - Breakthrough therapy designation is based on the encouraging survival data from the Phase 1 BrainChild-03 trial in ...

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