PharmaPoint Rheumatoid Arthritis - Drug Forecast and Market PharmaPoint Rheumatoid Arthritis - Drug Market
PharmaPoint Rheumatoid Arthritis - Drug Forecast and Market is
expected to grow to just over 8.5 million individuals by 2023:
Radiant Insights, Inc
Summary
Rheumatoid arthritis (RA) is a chronic autoimmune disease which causes inflammation and deformity of
the joints . It affects over seven million individuals in the 10MM covered in this report (US, France,
Germany, Italy, Spain, UK, Japan, Australia, China, and India) and the prevalence is expected to grow to
just over 8.5 million individuals by 2023. The anti-TNFs have been effective in treating the signs and
symptoms of RA and inhibiting progression to erosive bone disease. However, the landscape is quickly
changing with the introduction of biosimilars, novel biologics, and a class of oral therapies known as JAK
inhibitors, all of which will change the market dynamics between 2013 and 2023. With the anti-TNFs as
extremely effective therapies for RA, the market is extremely competitive for new entrants and will
undergo further pressure as biosimilars are approved and launch.
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Highlights
Key Questions Answered
- How large an impact will biosimilars have on the RA market? What do rheumatologists and key opinion
leaders across the 10MM think about the evolving RA treatment landscape?
- How is the uptake of JAK inhibitors expected to affect the global RA market?
- Which novel biologics are the most promising? How are product launches expected to affect the antiTNFs?
- According to KOLs, what are the most important unmet needs in RA? Will these needs be addressed by
pipeline agents? What needs will remain by the end of the forecast period in 2023?
- What governmental and industry developments are likely to affect sales of the top-selling RA drugs in
the markets researched? Which is the largest growth market globally?
Key Findings
- Biosimilars are expected to change the landscape for RA and create pricing pressure in the RA market.
However, questions from physicians and regulators regarding the appropriate use of biosimilars still
lingers.