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Aug 6, 2024
As reported in April this year, Celltrion presented the 78-week results of its Phase 3 study of CT-P41, biosimilar to Amgen’s Prolia® (denosumab), at the World Congress on Osteoporosis held in London from 11-14 April 2024. On 6 August 2024, Celltrion announced that...
Aug 6, 2024
On 6 August 2024, Health New Zealand announced that it will now allow a small group of cancer patients to receive free early access to MSD’s Keytruda® (pembrolizumab) despite deciding earlier this week that it would not do so. Pharmac is due to provide Keytruda®...
Aug 6, 2024
On 6 August 2024, Amgen announced its financial results for Q2/2024, reporting total revenues increased 20% to US$8.4 billion compared with Q2/2023. Twelve of its products delivered at least double-digit sales growth in the quarter, including Prolia® (denosumab),...
Aug 6, 2024
On 6 August 2024, MSD announced that it has expanded its existing global development and commercialisation agreement with Daiichi Sankyo to include MK-6070, a T-cell engager targeting delta-like ligand 3 (DLL3). Under the deal, the companies will jointly develop and...
Aug 5, 2024
On 5 August 2024, Lupin announced the successful completion of a global Phase III clinical study of LUBT010, its biosimilar to Genentech’s Lucentis® (ranibizumab). The study showed that LUBT010 has comparable efficacy, safety and immunogenicity to Lucentis® in...
Aug 2, 2024
On 2 August 2024, Australia’s Therapeutic Goods Administration announced that, according to Novo Nordisk, Wegovy® (semaglutide), specifically indicated for weight loss, will be available in Australia from early August 2024. While Wegovy® has been approved in Australia...
Aug 1, 2024
On 1 August 2024, Xbrane Biopharma announced that it will regain full rights to XcimzaneTM (BIIB801) biosimilar to UCB’s Cimzia® (certolizumab pegol) for rheumatoid arthritis and psoriasis. Xbrane and Biogen had entered into a commercialisation and licensing...
Aug 1, 2024
On 1 August 2024, Pharmacy Daily reported that Bristol Myers Squibb’s (BMS) Opdivo® (nivolumab) has had a new indication for resectable non-small cell lung cancer (NSCLC) listed on Australia’s Pharmaceutical Benefits Scheme (PBS). It now joins MSD’s Keytruda®...
Aug 1, 2024
On 1 August 2024, the PBS published its Summary of Changes, which included listing Pfizer’s Abrilada®, biosimilar to AbbVie’s Humira® (adalimumab), on the PBS in 20mg/0.4mL and 40mg/0.8mL dosage injections. This comes three years after Abrilada was first recommended...
Aug 1, 2024
On 1 August 2024, GSK announced that the FDA has approved Jemperli® (dostarlimab) in combination with carboplatin and paclitaxel followed by Jemperli® as a single agent for treating primary advanced or recurrent endometrial cancer. This expands the previous...
Aug 1, 2024
On 1 August 2024, Navlin Daily reported that Brazil’s National Commission for the Incorporation of Technologies into the Unified Health System (CONITEC) recommended against incorporating rituximab monotherapy in Brazil’s national health system for treating...
Jul 31, 2024
On 31 July 2024, Celltrion reported that Health Canada has approved its new drug licence application for Steqeyma (CT-P43), biosimilar to Janssen’s Stelara® (ustekinumab), for plaque psoriasis, psoriatic arthritis, and Crohn’s disease. The Health Canada approval...
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