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Fabry Disease – Pipeline Review, H1 2019 – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Fabry
Disease – Pipeline Review, H1 2019”
drug pipelines has been
added to ResearchAndMarkets.com’s offering.

Fabry Disease – Pipeline Review, H1 2019 provides
comprehensive information on the therapeutics under development for
Fabry Disease (Genetic Disorders), complete with analysis by stage of
development, drug target, mechanism of action (MoA), route of
administration (RoA) and molecule type.

The guide covers the descriptive pharmacological action of the
therapeutics, its complete research and development history and latest
news and press releases.

The Fabry Disease (Genetic Disorders) pipeline guide also reviews key
players involved in therapeutic development for Fabry Disease and
features dormant and discontinued projects.

The guide covers therapeutics under Development by
Companies/Universities/Institutes, the molecules developed by Companies
in Pre-Registration, Phase III, Phase II, Phase I, IND/CTA Filed and
Preclinical stages are 1, 2, 3, 1, 1 and 9 respectively. Similarly, the
Universities portfolio in Unknown stages comprises 1 molecules,
respectively.

Fabry Disease (Genetic Disorders) pipeline guide helps in identifying
and tracking emerging players in the market and their portfolios,
enhances decision making capabilities and helps to create effective
counter strategies to gain competitive advantage.

Scope

Reasons to Buy

Companies Mentioned

Key Topics Covered

  1. Introduction
  2. Overview
  3. Therapeutics Development
  4. Therapeutics Assessment
  5. Companies Involved in Therapeutics Development
  6. Dormant Projects
  7. Discontinued Products
  8. Product Development Milestones

For more information about this drug pipelines report visit https://www.researchandmarkets.com/r/k0rxmk

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Related
Topics: Endocrine
and Metabolic Disorders Drugs

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