Amgen receives Australian approval for Mvasi® (biosimilar bevacizumab) for all indications as Avastin®.
Home / Search Results
Stay informed about important legal and industry news with our blogs and weekly BioBlast® updates.
By Bioblast Editor | Jun 30, 2020
Amgen receives Australian approval for Mvasi® (biosimilar bevacizumab) for all indications as Avastin®.
By Bioblast Editor | Jun 30, 2020
Samsung Bioepis announces it has commenced Ph III trials of SB15, proposed aflibercept biosimilar.
By Bioblast Editor | Jun 30, 2020
Genentech files a complaint against Samsung Bioepis in the District Court of Delaware under the BPCIA, alleging infringement of 14 patents related to SB8 (Samsung’s proposed bevacizumab biosimilar), and violation of the “patent dance” provisions.
By Bioblast Editor | Jun 29, 2020
In a letter to the Editor published by the Washington Post, Keith Webber (former acting director of the FDA’s Office of Biotechnology Products and Office of Generic Drugs) highlighted the potential consequences of the legal brief filed in the US Supreme Court by the T...
By Naomi Pearce | Jun 29, 2020
Significant biosimilar activities this week include
June 20 | The NZ Herald reported a new study by NZ scientists which indicates that transgenic goats are capable of producing milk with high levels of cetuximab.
22 Jun 20 | Ankylosing Spondylitis News reported ...
By Bioblast Editor | Jun 29, 2020
Celltrion announces EU’s CHMP recommended expanding the marketing authorisation for its subcut Remsima® (biosimilar infliximab) to include the following additional indications: IBD, ankylosing spondylitis, Crohn’s disease, ulcerative colitis, psoriatic arthritis...
By Bioblast Editor | Jun 29, 2020
Merck announces the FDA has approved Keytruda® (pembrolizumab) for first-line treatment of patients with unresectable or metastatic microsatellite instability-high or mismatch repair deficient colorectal cancer.
By Bioblast Editor | Jun 29, 2020
Fujifilm Kyowa Kirin Biologics announces manufacturing and marketing approval in Japan for FKB237 (adalimumab biosimilar). This product was developed in partnership with Mylan and has been marketed as Hulio® in 20 countries across Europe.
By Bioblast Editor | Jun 28, 2020
Outlook India reports Dr Reddy’s is expecting to launch 25 products in the US market in the current financial year and that Dr Reddy’s Ph III trials of a proposed rituximab biosimilar are progressing as planned.
By Bioblast Editor | Jun 26, 2020
Janssen announces it has discontinued its Ph III LOTUS study of Stelara® (ustekinumab) in Systematic Lupus Erythematosus due to lack of efficacy.
SUBSCRIBE TO PEARCE IP