Fezolinetant (ESN364): Astellas’ Neurokinin 3 Receptor Antagonists Under Development for the Treatment of Vasomotor Symptoms – Global Emerging Insight and Market Forecast to 2030 – ResearchAndMarkets.com

March 9, 2021 Off By BusinessWire

DUBLIN–(BUSINESS WIRE)–The “Fezolinetant (ESN364) – Emerging Insight and Market Forecast – 2030” report has been added to ResearchAndMarkets.com’s offering.

“Fezolinetant (ESN364) – Emerging Insight and Market Forecast – 2030” the report provides comprehensive insights about an investigational product for Vasomotor symptoms in 7 Major Markets. A detailed picture of the Fezolinetant (ESN364) in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2020-2030 is provided in this report along with a detailed description of the product.

The product details cover mechanism of action, dosage and administration, route of synthesis, and Research and development activity including regulatory milestones, and other development activities. Further, it also consists of future market assessments inclusive of the market forecast, SWOT analysis, market competitors, and other emerging therapies.

Overview

Fezolinetant (ESN364) is a Neurokinin 3 receptor antagonists under development for the treatment of Vasomotor symptoms. It is being developed by Astellas. Fezolinetant (ESN364) is a proprietary, oral, small-molecule, discovered and developed by Ogeda for the purpose of the treatment of women’s health disorders. Fezolinetant is an antagonist of the GPCR known as the tachykinin NK3 receptor and acts on specific neurons that control body temperature to mimic the effects of estrogen, but in a non-hormonal manner, to directly and safely address the basis for HF in menopausal women.

Scope of the Report

  • A comprehensive product overview including the product description, mechanism of action, dosage and administration, Research and Development activity.
  • Elaborated details on regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the drug research and development activity details across the United States, Europe and Japan.
  • The report also covers the patents information with expiry timeline around Fezolinetant (ESN364).
  • The report contains forecasted sales for Fezolinetant (ESN364) till 2030.
  • Comprehensive coverage of the late-stage emerging therapies (Phase III) for Vasomotor symptoms.
  • The report also features the SWOT analysis with analyst insights and key findings of Fezolinetant (ESN364).

Fezolinetant (ESN364) Analytical Perspective

In-depth Fezolinetant (ESN364) Market Assessment

This report provides a detailed market assessment of Fezolinetant (ESN364) 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 forecasted sales data from 2020 to 2030.

Fezolinetant (ESN364) Clinical Assessment

The report provides the clinical trials information of Fezolinetant (ESN364) covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

  • In the coming years, the market scenario for Vasomotor symptoms is set to change due to the extensive research 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 Fezolinetant (ESN364) dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
  • Other emerging products for Vasomotor symptoms are giving market competition to Fezolinetant (ESN364) 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 development scenario of Fezolinetant (ESN364).
  • This in-depth analysis of the forecasted sales data of Fezolinetant (ESN364) from 2020 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Fezolinetant (ESN364).

Key Questions Answered

  • Which company is developing Fezolinetant (ESN364) along with the phase of the clinical study?
  • What is the technology utilized in the development of Fezolinetant (ESN364)?
  • What is the product type, route of administration and mechanism of action of Fezolinetant (ESN364)?
  • What is the clinical trial status of the study and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Fezolinetant (ESN364) development?
  • What are the key designations that have been granted to Fezolinetant (ESN364)?
  • What is the forecasted market scenario of Fezolinetant (ESN364)?
  • What is the history of Fezolinetant (ESN364) and what is its future?
  • What is the forecasted sales of Fezolinetant (ESN364) in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
  • What are the other emerging products available and how these are giving competition to Fezolinetant (ESN364)?
  • Which are the late-stage emerging therapies under development for the treatment of Vasomotor symptoms?

Key Topics Covered:

1. Drug Overview

1.1. Product Detail

1.2. Mechanism of Action

1.3. Dosage and Administration

1.4. Research and development activity

1.4.1. Clinical Development

1.4.2. Safety and Efficacy

1.5. Other Development Activities

2. Market Assessment

2.1. 7MM Market Analysis

2.2. The United States Market

2.3. Germany Market

2.4. France Market

2.5. Italy Market

2.6. Spain Market

2.7. United Kingdom Market

2.8. Japan Market

3. SWOT Analysis

4. Analyst Views

5. Market Competitors

6. Other Emerging Therapies

7. Appendix

For more information about this report visit https://www.researchandmarkets.com/r/q7m5ni

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

[email protected]

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

Fezolinetant (ESN364): Astellas’ Neurokinin 3 Receptor Antagonists Under Development for the Treatment of Vasomotor Symptoms – Global Emerging Insight and Market Forecast to 2030 – ResearchAndMarkets.com

March 9, 2021 Off By BusinessWire

DUBLIN–(BUSINESS WIRE)–The “Fezolinetant (ESN364) – Emerging Insight and Market Forecast – 2030” report has been added to ResearchAndMarkets.com’s offering.

“Fezolinetant (ESN364) – Emerging Insight and Market Forecast – 2030” the report provides comprehensive insights about an investigational product for Vasomotor symptoms in 7 Major Markets. A detailed picture of the Fezolinetant (ESN364) in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2020-2030 is provided in this report along with a detailed description of the product.

The product details cover mechanism of action, dosage and administration, route of synthesis, and Research and development activity including regulatory milestones, and other development activities. Further, it also consists of future market assessments inclusive of the market forecast, SWOT analysis, market competitors, and other emerging therapies.

Overview

Fezolinetant (ESN364) is a Neurokinin 3 receptor antagonists under development for the treatment of Vasomotor symptoms. It is being developed by Astellas. Fezolinetant (ESN364) is a proprietary, oral, small-molecule, discovered and developed by Ogeda for the purpose of the treatment of women’s health disorders. Fezolinetant is an antagonist of the GPCR known as the tachykinin NK3 receptor and acts on specific neurons that control body temperature to mimic the effects of estrogen, but in a non-hormonal manner, to directly and safely address the basis for HF in menopausal women.

Scope of the Report

  • A comprehensive product overview including the product description, mechanism of action, dosage and administration, Research and Development activity.
  • Elaborated details on regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the drug research and development activity details across the United States, Europe and Japan.
  • The report also covers the patents information with expiry timeline around Fezolinetant (ESN364).
  • The report contains forecasted sales for Fezolinetant (ESN364) till 2030.
  • Comprehensive coverage of the late-stage emerging therapies (Phase III) for Vasomotor symptoms.
  • The report also features the SWOT analysis with analyst insights and key findings of Fezolinetant (ESN364).

Fezolinetant (ESN364) Analytical Perspective

In-depth Fezolinetant (ESN364) Market Assessment

This report provides a detailed market assessment of Fezolinetant (ESN364) 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 forecasted sales data from 2020 to 2030.

Fezolinetant (ESN364) Clinical Assessment

The report provides the clinical trials information of Fezolinetant (ESN364) covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

  • In the coming years, the market scenario for Vasomotor symptoms is set to change due to the extensive research 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 Fezolinetant (ESN364) dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
  • Other emerging products for Vasomotor symptoms are giving market competition to Fezolinetant (ESN364) 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 development scenario of Fezolinetant (ESN364).
  • This in-depth analysis of the forecasted sales data of Fezolinetant (ESN364) from 2020 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Fezolinetant (ESN364).

Key Questions Answered

  • Which company is developing Fezolinetant (ESN364) along with the phase of the clinical study?
  • What is the technology utilized in the development of Fezolinetant (ESN364)?
  • What is the product type, route of administration and mechanism of action of Fezolinetant (ESN364)?
  • What is the clinical trial status of the study and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Fezolinetant (ESN364) development?
  • What are the key designations that have been granted to Fezolinetant (ESN364)?
  • What is the forecasted market scenario of Fezolinetant (ESN364)?
  • What is the history of Fezolinetant (ESN364) and what is its future?
  • What is the forecasted sales of Fezolinetant (ESN364) in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
  • What are the other emerging products available and how these are giving competition to Fezolinetant (ESN364)?
  • Which are the late-stage emerging therapies under development for the treatment of Vasomotor symptoms?

Key Topics Covered:

1. Drug Overview

1.1. Product Detail

1.2. Mechanism of Action

1.3. Dosage and Administration

1.4. Research and development activity

1.4.1. Clinical Development

1.4.2. Safety and Efficacy

1.5. Other Development Activities

2. Market Assessment

2.1. 7MM Market Analysis

2.2. The United States Market

2.3. Germany Market

2.4. France Market

2.5. Italy Market

2.6. Spain Market

2.7. United Kingdom Market

2.8. Japan Market

3. SWOT Analysis

4. Analyst Views

5. Market Competitors

6. Other Emerging Therapies

7. Appendix

For more information about this report visit https://www.researchandmarkets.com/r/q7m5ni

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

[email protected]

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

Fezolinetant (ESN364): Astellas’ Neurokinin 3 Receptor Antagonists Under Development for the Treatment of Vasomotor Symptoms – Global Emerging Insight and Market Forecast to 2030 – ResearchAndMarkets.com

March 9, 2021 Off By BusinessWire

DUBLIN–(BUSINESS WIRE)–The “Fezolinetant (ESN364) – Emerging Insight and Market Forecast – 2030” report has been added to ResearchAndMarkets.com’s offering.

“Fezolinetant (ESN364) – Emerging Insight and Market Forecast – 2030” the report provides comprehensive insights about an investigational product for Vasomotor symptoms in 7 Major Markets. A detailed picture of the Fezolinetant (ESN364) in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2020-2030 is provided in this report along with a detailed description of the product.

The product details cover mechanism of action, dosage and administration, route of synthesis, and Research and development activity including regulatory milestones, and other development activities. Further, it also consists of future market assessments inclusive of the market forecast, SWOT analysis, market competitors, and other emerging therapies.

Overview

Fezolinetant (ESN364) is a Neurokinin 3 receptor antagonists under development for the treatment of Vasomotor symptoms. It is being developed by Astellas. Fezolinetant (ESN364) is a proprietary, oral, small-molecule, discovered and developed by Ogeda for the purpose of the treatment of women’s health disorders. Fezolinetant is an antagonist of the GPCR known as the tachykinin NK3 receptor and acts on specific neurons that control body temperature to mimic the effects of estrogen, but in a non-hormonal manner, to directly and safely address the basis for HF in menopausal women.

Scope of the Report

  • A comprehensive product overview including the product description, mechanism of action, dosage and administration, Research and Development activity.
  • Elaborated details on regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the drug research and development activity details across the United States, Europe and Japan.
  • The report also covers the patents information with expiry timeline around Fezolinetant (ESN364).
  • The report contains forecasted sales for Fezolinetant (ESN364) till 2030.
  • Comprehensive coverage of the late-stage emerging therapies (Phase III) for Vasomotor symptoms.
  • The report also features the SWOT analysis with analyst insights and key findings of Fezolinetant (ESN364).

Fezolinetant (ESN364) Analytical Perspective

In-depth Fezolinetant (ESN364) Market Assessment

This report provides a detailed market assessment of Fezolinetant (ESN364) 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 forecasted sales data from 2020 to 2030.

Fezolinetant (ESN364) Clinical Assessment

The report provides the clinical trials information of Fezolinetant (ESN364) covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

  • In the coming years, the market scenario for Vasomotor symptoms is set to change due to the extensive research 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 Fezolinetant (ESN364) dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
  • Other emerging products for Vasomotor symptoms are giving market competition to Fezolinetant (ESN364) 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 development scenario of Fezolinetant (ESN364).
  • This in-depth analysis of the forecasted sales data of Fezolinetant (ESN364) from 2020 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Fezolinetant (ESN364).

Key Questions Answered

  • Which company is developing Fezolinetant (ESN364) along with the phase of the clinical study?
  • What is the technology utilized in the development of Fezolinetant (ESN364)?
  • What is the product type, route of administration and mechanism of action of Fezolinetant (ESN364)?
  • What is the clinical trial status of the study and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Fezolinetant (ESN364) development?
  • What are the key designations that have been granted to Fezolinetant (ESN364)?
  • What is the forecasted market scenario of Fezolinetant (ESN364)?
  • What is the history of Fezolinetant (ESN364) and what is its future?
  • What is the forecasted sales of Fezolinetant (ESN364) in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
  • What are the other emerging products available and how these are giving competition to Fezolinetant (ESN364)?
  • Which are the late-stage emerging therapies under development for the treatment of Vasomotor symptoms?

Key Topics Covered:

1. Drug Overview

1.1. Product Detail

1.2. Mechanism of Action

1.3. Dosage and Administration

1.4. Research and development activity

1.4.1. Clinical Development

1.4.2. Safety and Efficacy

1.5. Other Development Activities

2. Market Assessment

2.1. 7MM Market Analysis

2.2. The United States Market

2.3. Germany Market

2.4. France Market

2.5. Italy Market

2.6. Spain Market

2.7. United Kingdom Market

2.8. Japan Market

3. SWOT Analysis

4. Analyst Views

5. Market Competitors

6. Other Emerging Therapies

7. Appendix

For more information about this report visit https://www.researchandmarkets.com/r/q7m5ni

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

[email protected]

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