1 / 2

Biosimilars Evidence Whitepaper

Biosimilars Evidence: The US Biosimilars market perspectives on the current state of the Biosimilars in the United States<br>

yashb
Download Presentation

Biosimilars Evidence Whitepaper

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Biosimilars Evidence: The US Biosimilars market perspectives on the current state of the Biosimilars in the United States telegra.ph/Biosimilars-Evidence-The-US-Biosimilars-market-perspectives-on-the-current-state-of-the-Biosimilars-in- the-United-States-08-10 consulting services August 10, 2021 Biosimilars Evidence Whitepaper The first Biosimilars were made available to patients in the United States six years ago in 2021. These life-saving treatments have altered how Americans give and receive care. Without Biosimilars, the cost of biologics was expected to rise by 56 percent on average, limiting patients' access to treat patients. To ensure continuous access to the US market, bipartisan policy measures are required. Once these barriers are removed, the Biosimilars market in the United States will be able to fully exploit Biosimilars' true cost-saving potential. Through this Biosimilars Evidence Whitepaper, DelveInsight is representing the current state of Biosimilars in the U.S market. The Biosimilars is expanding therapeutic options in the USA, which is allowing the patients to start treatment with biological medications sooner. But there are certain challenges faced by Biosimilars to enter the United States market. To overcome the challenges the U.S FDA is updating its policies to reduce the difficulties or barriers that Biosimilars Evidence Whitepaper experience when entering the 1/2

  2. market. In the USA, the approved Biosimilars are for nine reference products, these are filgrastim, pegfilgrastim, bevacizumab, trastuzumab, infliximab, epoetin alfa, rituximab, etanercept, and adalimumab. The launch of these Biosimilars makes treatment more accessible to patients. Biosimilars are expected to break existing market share records in cancer treatment areas. These therapies are gaining market share at a much faster and greater rate than previously released Biosimilars. Biosimilars producers and regulators in the United States are gaining expertise and confidence, and technological advancements, as well as this type of science-based flexibility that will help the Biosimilars industry to grow in the United States market. Original Source:- https://www.delveinsight.com/whitepaper- newsletter/Biosimilars-evidence-in-the-united-states-whitepaper #healthcare #digitalhealth #healthtech #medtech #clinicaltrials #medicaldevices #research #biotech #data #health #opportunities #pharmaceuticalindustry #diagnostics #cancer #medicine #work #Biosimilarsevidence 2/2

More Related