GGS-CIDP by Tejin Pharma: An Intravenous, Freeze-dried Sulfonated Human Normal Immunoglobulin - Global Drug Insight and Market Forecast 2021-2030 - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "GGS-CIDP - Drug Insight and Market Forecast - 2030" report has been added to ResearchAndMarkets.com's offering.

"GGS-CIDP - Drug Insight and Market Forecast - 2030" report outlays comprehensive insights of the product indicated for the treatment of its approved condition. A detailed picture of the GGS-CIDP in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2017-2030 is provided in this report along with a detailed description of the product.

The product details covers mechanism of action, dosage and administration, route of synthesis, and pharmacological studies, including product marketed details, regulatory milestones, and other development activities. Further, it also consists of market assessments inclusive of the market forecast, SWOT analysis, and detailed analyst views. It further highlights the market competitors, late-stage emerging therapies, and patent details in the global space.

Drug Summary

GGS-CIDP (Tejin Pharma) is an intravenous, freeze-dried sulfonated human normal immunoglobulin which reported to shows high efficacy in restoring the lost muscle strength by its immune regulatory action of inhibiting the inflammation of the peripheral nerves; the drug thus offers promise as a treatment that will restore lost muscle strength. The drug is approved and marketed for the treatment of Chronic Inflammatory Demyelinating Syndrome.

GGS-CIDP Analytical Perspective

In-depth GGS-CIDP Market Assessment

This report provides a detailed market assessment of GGS-CIDP in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan. This segment of the report provides historical and forecasted sales data from 2017 to 2030.

GGS-CIDP Clinical Assessment

The report provides the clinical trials information of GGS-CIDP covering trial interventions, trial conditions, trial status, start and completion dates.

Scope of the Report

• A comprehensive product overview including the product description, mechanism of action, dosage and administration, route of synthesis, pharmacological studies (pharmacodynamics and pharmacokinetics) and adverse reactions.
• Elaborated details on regulatory milestones and other development activities have been provided in this report.
• The report also highlights the drug marketed details across the United States, Europe and Japan.
• The report also covers the patents information with expiry timeline around GGS-CIDP.
• The report contains historical and forecasted sales for GGS-CIDP till 2030.
• Comprehensive coverage of the late-stage emerging therapies (Phase III) in the space with a brief snapshot of the details.
• The report also features the SWOT analysis with analyst insights and key findings of GGS-CIDP.

Key Questions Answered

• What is the prescribed dosage and strengths of GGS-CIDP are available in the market?
• What are the common adverse reactions or side effects of GGS-CIDP?
• What is the product type, route of administration and mechanism of action of GGS-CIDP?
• What are the chemical specifications of GGS-CIDP?
• How are the clinical trials diversified on the basis of the trial status?
• What is the history of GGS-CIDP, and what is its future?
• What are the marketed details of GGS-CIDP in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
• How many patents have been granted to GGS-CIDP and when these patents will get expire?
• What are the pros (benefits) and cons (disadvantages) of GGS-CIDP?
• In which countries GGS-CIDP got approval and when it gets launched?
• What are the clinical trials are currently ongoing for GGS-CIDP?
• How the safety and efficacy results determined the approval of GGS-CIDP?
• What are the key collaborations, mergers and acquisitions, licensing and other activities related to the GGS-CIDP development?
• What are the key designations that have been granted to GGS-CIDP?
• What is the historical and forecasted market scenario of GGS-CIDP?
• How is the market trend of GGS-CIDP is different in the Seven Major Markets (the United States, EU5 [Germany, France, Italy, Spain, and the United Kingdom], and Japan)?
• What are the other approved products available and how these are giving competition to GGS-CIDP?
• Which are the late-stage emerging therapies under development for the treatment of the indicated condition?

Key Topics Covered:

1. Product Overview

1.1. Indication

1.2. Mechanism of Action

1.3. Dosage and Administration

1.3.1 Dosage Forms and Strengths

1.4. Route of Synthesis

1.5. Pharmacology

1.5.1 Pharmacodynamics

1.5.2 Pharmacokinetics

1.6. Adverse Reactions

1.7. Product Snapshot

1.8. Development Milestones of GGS-CIDP

1.9. Marketed Details

1.9.1 United States

1.9.2 Europe

1.9.3 Japan

1.10. Patent Details

2. SWOT Analysis

2.1. Analyst Views

3. Regulatory Milestones

3.1. Approvals

3.2. Research and Development

3.3. Clinical Trials Information

3.4. Safety and Efficacy

3.5. Product Developmental Activities

4. Market Assessment

4.1. 7MM Market Analysis

4.2. United States

4.3. Europe

4.4. Japan

4.5. Key Findings

5. Market Competitors

6. Emerging Therapies

7. Appendix

For more information about this report visit https://www.researchandmarkets.com/r/c681od