Biological Autoimmune Therapeutics Market, 2018-2022: Regulatory Factors, United State/FDA, Europe/EMA, Clinical Trial Protocols & Endpoints & Alliances and Partnerships
DUBLIN, Nov. 20, 2018 /PRNewswire/ --
The "Biological Autoimmune Therapeutics" report has been added to ResearchAndMarkets.com's offering.
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This report describes key factors in the trend toward user acceptance and designed-in usability. The influence of biosimilars on as-supplied packaging strategies is yet to be determined, but the need for product differentiation in an increasingly crowded market segment will make product packaging a key competitive factor.
The administration of therapeutic immune modulators is becoming an increasingly important healthcare treatment option for a growing number of diseases and indications having broad implications for patient health and well-being. But to fully exploit the value of this class of therapeutics in both human and commercial terms, developers must successfully navigate the inherent limitations of drug storage and administration, moving away from infusion and toward injection as a route of administration.
Antibody drug products indicated for chronic conditions such as autoimmunity are often re-formulated, re-packaged and re-labeled into injectable form and re-introduced two to three years post-market launch to address the growing economic pressure and patient desire to avoid the need for out-patient infusion in favor of self-injection.
Biological Autoimmune Therapeutics - What You Will Learn
-- What are the approved biological drugs indicated for autoimmune
conditions, what is the as-supplied packaging, and who markets them?
-- What are the major factors driving the growth of biological drugs for
treating autoimmunity?
-- What is the size of the market biological autoimmune therapeutics drugs
today, who are the market share leaders, and what will it be in 2022?
-- How important are drug developer-device manufacturer relationships and
what are the key alliances in the industry?
-- What are the essential design factors, technologies and market
development issues for biological autoimmune drugs?
-- What are the significant economic, technology, and regulatory factors
affecting the market for immunotherapeutic drugs?
Key Topics Covered:
Executive Summary
Market Dynamics
-- Unmet Patient Needs
-- Drug Development
-- Patient Population Factors
The Autoimmune Patient
-- The Informed Patient
-- Product Design & Patient Enablement Factors
-- Ease of Use
-- Patient Adherence
-- Dosing Frequency
Product Landscape
-- Biosimilars
-- Regional Market Product Strategies
As-Supplied Packaging and Administration
-- Device Selection - Stability and Material Issues
-- Human Engineering/Ergonomics
-- Pre- and Post-Marketing Device Evolution
-- The Role of Prefilled Devices
-- Prefilled Syringes
-- Autoinjectors
-- Special Feature Autoinjectors
-- Pen Injectors
-- Emerging Devices
The Product Ecosystem
-- Supplier Relationships
-- Supplier Resources - Geographic Distribution
-- Drug Supply Chain Activity
Product Analysis, Financial Performance & Forecasts
Development-stage Therapeutics
Autoimmune Therapeutics - Market Segment Analysis
-- Ankylosing Spondylitis
-- Crohn's Disease
-- Adult Rheumatoid Arthritis
-- Juvenile Idiopathic Arthritis
-- Multiple Sclerosis
-- Psoriatic Arthritis
-- Ulcerative Colitis
Market Factors
-- Regulatory Factors
-- United State/FDA
-- Europe/EMA
-- Clinical Trial Protocols & Endpoints
-- Alliances and Partnerships
Company Profiles
For more information about this report visit https://www.researchandmarkets.com/research/32x9tr/biological?w=5
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