Providing news & information about biosimilars—biologic medicines that are FDA-approved based on similarity to an existing biological. RT ≠ Endorsement.
Phase 3 clinical trials have started for the biosimilar drug treating plaque psoriasis, which also intends to treat treat autoimmune diseases such as psoriatic arthritis, Crohn's disease, and ulcerative colitis.
https://t.co/5jwPKxHdti
It is more crucial than ever that #misinformation on #biosimilars be addressed by the federal government, especially on issues of effectiveness and efficacy.
https://t.co/9nmDj3MD1I
The #biosimilars industry can learn valuable lessons and best practices from generic medicines. Hear in a new @AJMC_Journal podcast on how the U.S. generics industry could be instructive in understanding how biosimilar sales may develop over time.
https://t.co/dfkx1ytJQ4
From @FitchRatings: "Regulatory and legislative steps are underway to increase biosimilar uptake, given biosimilars are less expensive and highly similar alternatives to higher cost biologics."
https://t.co/aqjTvSWnKZ
A #NEW@ASCPTjournals study: Medicare would have saved $2.19 billion on adalimumab spending between 2016 and 2019 had #biosimilars become available in the years they were approved.
Read more study insights from the @BiosimCenter: https://t.co/qEyfLN1kVu
#ICYMI: President Biden outlined his administration's support for #biosimilars expansion in an Executive Order, directing @HHSGov to increase their support of biosimilars in the U.S. market.
https://t.co/5Idttaqpnz
Kevin Dunleavy of @FiercePharma profiles the expansive growth of #biosimilars and cost savings. He speaks to Bernstein analyst Ronny Gal, who adds biosimilars have been a "moderating force on drug prices."
https://t.co/ariouDft9y
@AJMC_Journal interviewed Dr. Ivo Abraham on #COVID's impact on #biosimilars.
He concluded: "We realize biosimilars, certainly the ones in the United States, are just as good as the reference products and we don't have to worry about safety."
https://t.co/zxDEQDUHqR
#ICYMI: @AccessibleMeds, along with 25+ patient and provider groups, extended support for the #BIOSIMAct in Congress.
This legislation would incentivize physicians to prescribe #biosimilars.
https://t.co/oJtwI70hr4
Authors of a recent @BioDrugsJournal op-ed argue there is a double standard for #biosimilars data and review, calling for "efficiency of development and review because such improvements in efficiency can allow more competition in the marketplace."
https://t.co/ul1i6D5Rd0
Soon, Europe, Canada, Israel and New Zealand will see a new commercialized #biosimilar on the market.
Teva and Bioeq are partnering for the commercialization of FYB201, a biosimilar to treat macular degeneration.
https://t.co/vzYlkYDjy8
#News from the UK: Updated regulatory guidance that reduces unnecessary clinical trials could put the UK ahead of Europe and facilitate a #biosimilars boom.
Read the full analysis on this change from the @PharmaReview: https://t.co/xPndZe8XEH
Oncology is expensive, but "biosimilars present an opportunity to reduce Medicare spending without impacting the quality of care provided to patients," writes Keely Macmillan in @AJMC_Journal.
https://t.co/QvlmjiR9VN
Jair Hilburn of @ForbesScience writes on the price-reducing potential of #biosimilars: "They are not only less expensive than brand name biologics themselves, they also apply competitive pressure to the brand name drugs."
https://t.co/p1ntzWzTuW
This new piece from @Sandoz_Global highlights last month's @Reuters event about unlocking the potential of #biosimilars, where I explained how increased adoption of biosimilars in the U.S. would provide massive savings for patients and taxpayers alike.
https://t.co/sTLmsA2wUk