Telix Pharmaceuticals announced that the FDA has designated Telix’s monoclonal antibody TLX66 (90Y-besilesomab) an orphan drug for use in conditioning treatment of bone marrow prior to hematopoietic stem cell transplant.
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By Bioblast Editor | Mar 29, 2022
Telix Pharmaceuticals announced that the FDA has designated Telix’s monoclonal antibody TLX66 (90Y-besilesomab) an orphan drug for use in conditioning treatment of bone marrow prior to hematopoietic stem cell transplant.
By Bioblast Editor | Mar 29, 2022
Formycon and Athos KG announced that they have agreed to enter into a long-term strategic partnership regarding biosimilars. As part of this agreement, Formycon will acquire 100% of the rights in FYB202 (biosimilar ustekinumab candidate) and a 50% stake in FYB201 (biosimil...
By Bioblast Editor | Mar 29, 2022
Lannett announced that it has commenced dosing in its pivotal trial of biosimilar insulin glargine.
By Naomi Pearce | Mar 29, 2022
19 Mar 22 | US | Amgen and Pfizer settled their pegfilgrastim (Neulasta®) dispute Amgen Inc v Hospira Inc (D. Del., No. 20-201) which has been on foot since February 2020. No furth...
By Bioblast Editor | Mar 28, 2022
Medical Xpress reports on an Institute of Cancer Research, London, study showing that levels of the protein PD-L1 detected in head and neck tumours can be used to personalise medicine. Depending on PD-L1 levels, patients should receive personalised medicine of either chemo...
By Bioblast Editor | Mar 28, 2022
Aurobindo announced that it will acquire certain business assets from Veritaz (the supplier of branded generic formulations and other health care products) for Rs 171 crore on a debt free basis. The acquisition will support Aurobindo’s plans to manufacture biosimilars and ...
By Bioblast Editor | Mar 25, 2022
The Office of the Assistant Secretary for Preparedness and Response has announced that it will pause the distribution of sotrovimab in certain US states in which the BA.2 variant has become the dominant COVID-19 strain. This announcement follows FDA advice which indicates ...
By Bioblast Editor | Mar 25, 2022
Australia’s TGA approved Celltrion’s Yuflyma® (biosimilar to AbbVie’s Humira® (adalimumab) for the treatment of rheumatoid arthritis, juvenile idiopathic arthritis, enthesitis-related arthritis, psoriatic arthritis, ankylosing spondylitis. Crohn’s disease, ulcer...
By Naomi Pearce | Mar 25, 2022
Commissioner of Patents v Ono Pharmaceutical Co. Ltd & Anr [2022] FCAFC 39
Date:
Court:
Judges:
18 March 2022
Full Federa...
By Naomi Pearce | Mar 25, 2022
Merck Sharp & Dohme & Anor v Sandoz Pty Ltd [2022] FCAFC 40
Date:
Court:
Judges:
18 March 2022
Full Federal Court of ...
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