New Report Explores Hottest Trends in Biosimilar Drug Market 2020-2025: Global Key Vendors - Amgen, Eli Lilly, Novartis, CP Guojian Pharma, Biotech Pharma

Global Biosimilar Drug Market Synopsis:

The exclusive research report on the Global Biosimilar Drug Market 2020-2025 examines the market in detail along with focusing on significant market dynamics for the key players operating in the market. Global Biosimilar Drug Industry research report offers granulated yet in-depth analysis of revenue share, market segments, revenue estimates and various regions across the globe.

Major key factors driving the growth of the Global Biosimilar Drug Market are rapid growth in incidences of chronic diseases globally, coupled with the cost-effectiveness of biosimilars. In addition, the development of biosimilars for new indications and the patent expiry of biologic drugs are expected to offer significant growth opportunities to the Biosimilar Drug Market players in the coming years.

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Significant points in table of contents: Market Definition, Market Overview, Business Introduction, Segmentation (Region Level), Segmentation (Type Level), Segmentation (Industry Level), Segmentation (Channel Level), Market Forecast Year, Segmentation Type, Segmentation Industry, Market Cost Analysis, and Conclusion. The Biosimilar Drug Market is segmented based on Product, source, application and Regions. On the basis of product, the market is sub-segmented.

Regionally, North America and Europe holds major share in Global Biosimilar Drug Market. Moreover, Asia-Pacific is expected to record higher growth rate in Biosimilar Drug market during the forecast year.

Top Major Key Players in the Global Biosimilar Drug Market:

1 Amgen

2 Eli Lilly

3 Novartis

4 CP Guojian Pharma

5 Biotech Pharma and More............

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Product Type Segmentation

1 Injection

2 Tablets

3 Other Types

Industry Segmentation

1 Ankylosing Spondylitis

2 Tumor

3 Rheumatoid Arthrtis

4 Cardiovascular

Top Medical Industry News:

Novartis (March 19, 2020) - Novartis receives approval from Japanese Ministry of Health, Labour and Welfare for Zolgensma the only gene therapy for patients with spinal muscular atrophy (SMA) - Novartis Pharma K.K. ("Novartis Pharma") today announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) approved Zolgensma (onasemnogene abeparvovec) for the treatment of spinal muscular atrophy (SMA) in patients under the age of two, including those who are pre-symptomatic at diagnosis. Patients must be negative for elevated anti-AAV9 antibodies. A rare, genetic neuromuscular disease caused by a lack of a functional SMN1 gene, SMA results in the rapid and irreversible loss of motor neurons, affecting muscle functions, including breathing, swallowing and basic movement. Approximately 60% of all SMA is Type 1. Zolgensma is a one-time gene therapy designed to address the genetic root cause of the disease by replacing the function of the missing or nonworking SMN1 gene. Zolgensma is administered during a single intravenous (IV) infusion, delivering a new working copy of the SMN gene into a patient's cells, halting disease progression. Approximately 15-20 SMA patients in Japan are expected to be eligible for treatment each year. Reimbursement with MHLW is expected by the end of 1H20 and, pending agreement, Zolgensma will be available at that time.

"SMA is the leading genetic cause of infant death and, if left untreated in its most common form, Type 1, leads to death or the need for permanent ventilation by the age of two in more than 90% of cases," said Kazunari Tsunaba, president and representative director, Novartis Pharma. "A one-time dose of Zolgensma has the potential to make a truly transformative impact on this life-threatening disease. This is an important day for the children and families in Japan impacted by SMA, both today and in the future."

The most commonly observed side effects after treatment were elevated liver enzymes and vomiting. Acute serious liver injury and elevated aminotransferases can occur. Patients with pre-existing liver impairment may be at higher risk. Prior to infusion, physicians should assess liver function of all patients by clinical examination and laboratory testing. And, they should administer systemic corticosteroid to all patients before and after treatment, and then continue to monitor liver function for at least 3 months after infusion.

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Major Points in Table of Contents:

Global Biosimilar Drug Market Report 2020

1 Biosimilar Drug Product Definition

2 Global Biosimilar Drug Market Manufacturer Share and Market Overview

2.1 Global Manufacturer Biosimilar Drug Shipments

2.2 Global Manufacturer Biosimilar Drug Business Revenue

2.3 Global Biosimilar Drug Market Overview

3 Manufacturer Biosimilar Drug Business Introduction

3.1 Amgen Biosimilar Drug Business Introduction

3.2 Eli Lilly Biosimilar Drug Business Introduction

3.3 Novartis Biosimilar Drug Business Introduction

3.4 CP Guojian Pharma Biosimilar Drug Business Introduction

3.5 Biotech Pharma Biosimilar Drug Business Introduction

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