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Age Related Macular Degeneration Market to Grow with an Impressive CAGR by 2023 | Analysis by Pfizer, Bayer, Roche
Age Related Macular Degeneration Market
Global Age Related Macular Degeneration (AMD) Market Overview:
The Global Age Related Macular Degeneration (AMD) Market research report is the investigation arranged by investigators, which contain a point by point examination of drivers, limitations, and openings alongside their effect on the Age Related Macular Degeneration (AMD) Market development (2019 - 2023).
According to the market research report, increasing reimbursement benefits for Age Related Macular Degeneration (AMD) drugs supplements the market growth. Furthermore, a surge in the prevalence of eyerelated disorders and a rise in the global geriatric population boost the Age Related Macular Degeneration (AMD) Market. However, increase in the use of offlabel drugs and availability of offlabel therapies impedes the growth of the market.
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The Global Age Related Macular Degeneration (AMD) Market is segmented on the basis of Type, End-User and Region. Age Related Macular Degeneration (AMD) market is cover distinctive segment market estimate, both volume and value, also cover diverse businesses customers' data, which is imperative for the makers.
Based on the Type, the Global Age Related Macular Degeneration (AMD) Market is sub-segmented into Wet AMD, Dry AMD and others. On the basis of End-User, the Global Age Related Macular Degeneration (AMD) Market is classified into Men, Woman and others.
In terms of the geographic analysis, The Age Related Macular Degeneration (AMD) Market in North America is expected to grow at the highest CAGR during the forecast period. Moreover, the presence of major players in the Age Related Macular Degeneration (AMD) Market ecosystem results in the increasing adoption of these systems in North America.
Latest Industry News:
Pfizer () – Pfizer Presents Interim Analysis Results From Phase 3 Beacon Crc Trial Of Braftovi (Encorafenib), Mektovi (Binimetinib) And Cetuximab For The Treatment Of Brafv600e-Mutant Metastatic Colorectal Cancer – Pfizer Inc., today announced detailed results from the interim analysis of the Phase 3 BEACON CRC trial evaluating the combination of BRAFTOVI (encorafenib), MEKTOVI® (binimetinib), and cetuximab (BRAFTOVI Triplet), in patients with advanced BRAFV600E-mutant metastatic colorectal cancer (mCRC), following one or two lines of therapy. The results show significant improvements in overall survival (OS) and objective response rates (ORR) for the BRAFTOVI Triplet and BRAFTOVI Doublet combination (BRAFTOVI and cetuximab), compared to cetuximab plus irinotecan-containing regimens (Control), and provide analysis of the efficacy and safety of the BRAFTOVI Triplet compared to the BRAFTOVI Doublet. These data will be presented today during a late-breaking oral session at the 2019 European Society for Medical Oncology (ESMO) Congress in Barcelona, Spain, and simultaneously published online in The New England Journal of Medicine (NEJM). Pfizer intends to submit the results of the BEACON CRC trial for marketing approval in the U.S. in the fourth quarter of 2019. The use of BRAFTOVI, MEKTOVI and cetuximab for the treatment of patients with BRAFV600E-mutant mCRC is investigational and not approved by the FDA.
As previously announced, the BRAFTOVI Triplet showed a median OS of 9.0 months for patients treated with the Triplet, compared to 5.4 months for Control ([HR 0.52, (95% CI 0.39-0.70), p
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