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Mydriasert: An Ophthalmic Insert Containing 0.28mg Tropicamide and 5.4mg Phenylephrine Hydrochloride - Global Drug Insight and Market Forecast to 2030 - ResearchAndMarkets.com

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

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

Mydriasert is an ophthalmic insert containing 0.28mg tropicamide and 5.4mg phenylephrine hydrochloride. Mydriasert is indicated to obtain pre-operative mydriasis or for diagnostic purposes where monotherapy is known to be insufficient. It is an ophthalmic pellet inserted into the lower conjunctival fornix prior to surgery or diagnostic procedure. It is marketed by Thea Pharmaceuticals.

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
  • The report contains historical and forecasted sales for Mydriasert 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 Mydriasert.

Mydriasert Analytical Perspective

In-depth Mydriasert Market Assessment

This report provides a detailed market assessment of Mydriasert 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.

Mydriasert Clinical Assessment

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

Report Highlights

  • In the coming years, the market scenario for Mydriasert is set to change due to the extensive research in the treatment of the indicated condition and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
  • The companies and academics are working to assess challenges and seek opportunities that could influence Mydriasert dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
  • Other approved products for the disease are giving market competition to Mydriasert and launch of late-stage emerging therapies in the near future will significantly impact the market.
  • A detailed description of regulatory milestones, development activities, and some key findings provide the current market scenario of Mydriasert.
  • This in-depth analysis of the sales data of Mydriasert from 2017 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Mydriasert in the market.

Key Questions Answered

  • What is the prescribed dosage and strengths of Mydriasert are available in the market?
  • What are the common adverse reactions or side effects of Mydriasert?
  • What is the product type, route of administration and mechanism of action of Mydriasert?
  • What are the chemical specifications of Mydriasert?
  • How are the clinical trials diversified on the basis of the trial status?
  • What is the history of Mydriasert, and what is its future?
  • What are the marketed details of Mydriasert 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 Mydriasert and when these patents will get expire?
  • What are the pros (benefits) and cons (disadvantages) of Mydriasert?
  • In which countries Mydriasert got approval and when it gets launched?
  • What are the clinical trials are currently ongoing for Mydriasert?
  • How the safety and efficacy results determined the approval of Mydriasert?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Mydriasert development?
  • What are the key designations that have been granted to Mydriasert?
  • What is the historical and forecasted market scenario of Mydriasert?
  • How is the market trend of Mydriasert 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 Mydriasert?
  • 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 Mydriasert

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/lzrf9e

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Research and Markets


Release Versions

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

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