On 27 June 2024, Korea Biomedical Review reported that Samsung Bioepis intends to launch its ustekinumab biosimilar Epyztek™ in Korea in July 2024. The product will be supplied at a 40% discount to J&J’s Stelara® (ustekinumab).
On 27 June 2024, Coherus BioSciences announced that it has agreed to divest its Yusimry™, biosimilar to AbbVie’s Humira (adalimumab), to Hong Kong King-Friend (HKF) for up-front all-cash consideration of USD $40M. On the same day, Meitheal Pharmaceuticals, wholly owned sub...
We are delighted that Pearce IP has been honoured as Australasian Lawyer’s 2024 Top Boutique Firm in the category of Intellectual Property. Australasian Lawyer has selected 47 firms...
At its June 2024 meeting, EMA’s Committee for Medicinal Products for Human Use (CHMP) issued a positive opinion for Celltrion’s Steqeyma (CT-P43), biosimilar to Janssen’s Stelara® (ustekinumab). The recommendation is for moderately to severely active Crohn’s disease, plaqu...
On 27 June 2024, Harbour Biomed announced that it has resubmitted its Biologics License Application (BLA) for batoclimab (HBM9161) to the China’s National Medical Products Administration (NMPA) for the treatment of generalized myasthenia gravis. The resubmission voluntarily...
Novo Nordisk announced that Wegovy® has been approved in China for long-term weight management, targeting patients with a BMI of 30kg/m² and at least one weight-related comorbidity.
The approval comes as the company plans a $4.1 billion expansion of its US manufac...
On 25 June 2024, Simcere Zaiming announced the approval of Enlituo® (cetuximab beta) in the PRC for use in combination with the FOLFIRI regimen as a first-line treatment for RAS/BRAF wild-type metastatic colorectal cancer (mCRC). The drug was developed in collaboration with...
In the life sciences field, using multiple claim types to protect inventions can be crucial to a comprehensive patenting strategy. For novel biologics and pharmaceuticals, claims t...
On 26 June 2024, AbbVie announced that its Epkinly® (epcoritamab) received FDA approval for the treatment of adults with relapsed or refractory follicular lymphoma. This approval makes Epkinly® the first and only subcutaneous bispecific antibody approved in the US to treat...
On 25 June 2024, Novo Nordisk announced its plan to significantly boost its investment in manufacturing in 2024, allocating USD $6.8 billion towards production. This is up from USD $3.9 billion the previous year.
The plan includes a USD $4.1 billion investment to ...
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