Unexpected Growth Seen in Blood Compatible Polymers Market Global Forecast to 2025 | Sanofi, AdvanSource Biomaterials, Baxter, ASM International, Biomaterial USA, Evonik, DowDuPont

The exclusive research report on the Global Blood Compatible Polymers Market 2020 examines the market in detail along with focusing on significant market dynamics for the key players operating in the market. Global Blood Compatible Polymers Industry research report offers granulated yet in-depth analysis of revenue share, market segments, revenue estimates and various regions across the globe.

Overview of Global Blood Compatible Polymers Market:

This report studies the Global Blood Compatible Polymers Market over the forecast period of 2020 to 2025. The Global Blood Compatible Polymers Market is expected to grow at an impressive Compound Annual Growth Rate (CAGR) from 2020 to 2025.

One of the most important key factor drives the growth of the Global Blood Compatible Polymers Market is biomedical and pharmaceutical end-use industries. The Blood Compatible Polymers have various advantages over the other biomedical devices. They have been used extensively used over the last two decades. However, blood compatible polymers need to be made at a particular composition of polymers. Several techniques are used to gain desired properties of polymers to make them blood compatible. These techniques need highly skilled workers and adequate laboratory facilities. Hence, lack of skilled workers and laboratory facilities are likely to restrain the Global Blood Compatible Polymers Market.

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The Global Blood Compatible Polymers Market is segmented on the basis of Type, Application and Region. Based on the Type, the Global Blood Compatible Polymers Market is sub-segmented into Polyvinylchloride, Polytetrafluoroethylene, Polyethersulfone, Polyethylene, Polyetheretherketone / Polysulfone / Poly Propalene and others. On the basis of Application, the Global Blood Compatible Polymers Market is classified into Biomedical & Blood Contacting Devices, Dental, Drug delivery and others.

In terms of the geographic analysis, The Blood Compatible Polymers Market in North America is expected to grow at the highest CAGR during the forecast period. Moreover, the presence of major players in the Blood Compatible Polymers Market ecosystem results in the increasing adoption of these systems in North America.

Global Blood Compatible Polymers Market Objectives:

1 To provide detailed information regarding key factors (drivers, restraints, opportunities, and industry-specific challenges) influencing the growth of the Blood Compatible Polymers Market

2 To analyze and forecast the size of the Blood Compatible Polymers Market, in terms of value and volume

3 To analyze opportunities in the Blood Compatible Polymers Market for stakeholders and provide a competitive landscape of the market

4 To define, segment, and estimate the Blood Compatible Polymers Market based on deposit type and end-use industry

5 To strategically profile key players and comprehensively analyze their market shares and core competencies

6 To strategically analyze micromarkets with respect to individual growth trends, prospects, and contribution to the total market

7 To forecast the size of market segments, in terms of value, with respect to main regions, namely, Asia Pacific, North America, Europe, the Middle East & Africa, and South America

8 To track and analyze competitive developments, such as new product developments, acquisitions, expansions, partnerships, and collaborations in the Blood Compatible Polymers Market

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Top Leading Key Manufacturers are: AdvanSource Biomaterials, Sanofi, Baxter International, ASM International, Biomaterial USA, Eastman Chemical Company, Evonik Industries AG, DowDuPont, Jiangsu Senolo Medical Technology, TOPAS Advanced Polymers GmbH and others. New product launches and continuous technological innovations are the key strategies adopted by the major players.

Worldwide Medical Industry News:

Sanofi (May 22, 2020) - Dupixent (dupilumab) eosinophilic esophagitis trial meets both co-primary endpoints - Sanofi and Regeneron Pharmaceuticals, Inc. today announced positive results from Part A of the pivotal Phase 3 trial evaluating Dupixent (dupilumab) in patients 12 years and older with eosinophilic esophagitis (EoE). The trial met both of its co-primary endpoints, as well as all key secondary endpoints. Dupixent is the first and only biologic to show positive and clinically-meaningful results in this population as part of a Phase 3 trial. An on-going Part B portion of the Phase 3 trial evaluates an additional Dupixent dosing regimen.

EoE is a chronic and progressive type 2 inflammatory disease that damages the esophagus and prevents it from working properly, leading to difficulties swallowing. If untreated, symptoms and inflammation can progress, causing functional damage and scarring of the esophagus. EoE can lead to esophageal food impaction, requiring immediate emergency room visits. Almost half of the patients in this trial had prior procedures such as dilation of their esophagus, and almost three-quarters had previously been treated with corticosteroids. In the U.S., there are approximately 160,000 patients with EoE who are currently treated, of which an estimated 50,000 have failed multiple treatments. There are currently no therapies approved by the U.S. Food and Drug Administration (FDA).

"Eosinophilic esophagitis can be debilitating, and there are no approved treatment options. It impacts patients' ability to eat, causes severe pain and often results in repeated emergency room visits and medical procedures," said George D. Yancopoulos, M.D., Ph.D., Co-Founder, President and Chief Scientific Officer of Regeneron. "These data are particularly impressive as Dupixent not only dramatically reduced eosinophils in the esophagus, but also improved all clinical, anatomic and histologic measures of the disease. In the past, EoE was thought to be a disease caused by eosinophils, but other biologics that decrease the eosinophils in the esophagus did not demonstrate consistent clinical or anatomical improvements. These Dupixent results demonstrate EoE is caused by multiple aspects of type 2 inflammation, driven by interleukin-4 and interleukin-13. EoE is the fourth atopic or type 2 inflammatory disease in which Dupixent has pivotal data demonstrating significant efficacy."'

"These data demonstrate Dupixent's potential to continue to address treatment gaps across the spectrum of type 2 inflammatory diseases as common as asthma and as rare as eosinophilic esophagitis," said John Reed, M.D, Ph.D, Global Head of Research and Development at Sanofi. "For the first time in a Phase 3 trial, patients reported an improvement in their ability to swallow food. For patients with eosinophilic esophagitis who are living with restricted diets and, in some cases, repeated hospital interventions, these findings are encouraging."

Part A of the trial enrolled 81 patients (42 with Dupixent, 39 with placebo) aged 12 years and older with EoE, as determined by histological and patient-reported measures. The co-primary endpoints assessed the change from baseline in the Dysphagia Symptom Questionnaire (DSQ), a patient-reported measure of difficulty swallowing, and the proportion of patients achieving peak esophageal intraepithelial eosinophil count of

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