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Wilson Disease Drugs in Development by Stages, Target, MoA, RoA, Molecule Type and Key Players, 2022 Update

Publisher Global Markets Direct
Published Nov 30, 2022
Length 59 Pages
SKU # GMD17776515

Description

Wilson Disease Drugs in Development by Stages, Target, MoA, RoA, Molecule Type and Key Players, 2022 Update

Summary

Global Markets Direct's latest Pharmaceutical and Healthcare disease pipeline guide Wilson Disease - Drugs In Development, 2022, provides an overview of the Wilson Disease (Genetic Disorders) pipeline landscape.

Wilson disease is a rare autosomal recessive inherited disorder of copper metabolism that is characterized by excessive deposition of copper in the liver, brain, and other tissues. Symptoms include abdominal pain, jaundice, problems with speech, swallowing and muscle stiffness. Treatment includes chelators and Vitamin E supplements.

Report Highlights

Global Markets Direct's Pharmaceutical and Healthcare latest pipeline guide Wilson Disease - Drugs In Development, 2022, provides comprehensive information on the therapeutics under development for Wilson 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 Wilson Disease (Genetic Disorders) pipeline guide also reviews of key players involved in therapeutic development for Wilson Disease and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Phase III, Phase II, Preclinical and Discovery stages are 2, 1, 4 and 7 respectively.

Wilson 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. The guide is built using data and information sourced from Global Markets Direct’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.

Note:Certain content / sections in the pipeline guide may be removed or altered based on the availability and relevance of data.

Scope
  • The pipeline guide provides a snapshot of the global therapeutic landscape of Wilson Disease (Genetic Disorders).
  • The pipeline guide reviews pipeline therapeutics for Wilson Disease (Genetic Disorders) by companies and universities/research institutes based on information derived from company and industry-specific sources.
  • The pipeline guide covers pipeline products based on several stages of development ranging from pre-registration till discovery and undisclosed stages.
  • The pipeline guide features descriptive drug profiles for the pipeline products which comprise, product description, descriptive licensing and collaboration details, R&D brief, MoA & other developmental activities.
  • The pipeline guide reviews key companies involved in Wilson Disease (Genetic Disorders) therapeutics and enlists all their major and minor projects.
  • The pipeline guide evaluates Wilson Disease (Genetic Disorders) therapeutics based on mechanism of action (MoA), drug target, route of administration (RoA) and molecule type.
  • The pipeline guide encapsulates all the dormant and discontinued pipeline projects.
  • The pipeline guide reviews latest news related to pipeline therapeutics for Wilson Disease (Genetic Disorders)
Reasons to Buy
  • Procure strategically important competitor information, analysis, and insights to formulate effective R&D strategies.
  • Recognize emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
  • Find and recognize significant and varied types of therapeutics under development for Wilson Disease (Genetic Disorders).
  • Classify potential new clients or partners in the target demographic.
  • Develop tactical initiatives by understanding the focus areas of leading companies.
  • Plan mergers and acquisitions meritoriously by identifying key players and it’s most promising pipeline therapeutics.
  • Formulate corrective measures for pipeline projects by understanding Wilson Disease (Genetic Disorders) pipeline depth and focus of Indication therapeutics.
  • Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope.
  • Adjust the therapeutic portfolio by recognizing discontinued projects and understand from the know-how what drove them from pipeline.

Table of Contents

59 Pages
Introduction
Global Markets Direct Report Coverage
Wilson Disease – Overview
Wilson Disease – Therapeutics Development
Pipeline Overview
Pipeline by Companies
Products under Development by Companies
Wilson Disease – Therapeutics Assessment
Assessment by Target
Assessment by Mechanism of Action
Assessment by Route of Administration
Assessment by Molecule Type
Wilson Disease – Companies Involved in Therapeutics Development
Alexion Pharmaceuticals Inc
ARBORMED Pharmaceuticals Inc
Deep Genomics Inc
DepYmed Inc
Enveda Biosciences Inc
Generation Bio Co
Krisani Bio Sciences Pvt Ltd
LambdaGen Therapeutics
Logicbio Therapeutics Inc
MeiraGTx Holdings Plc
Shanghai Pharmaceuticals Holding Co Ltd
Ultragenyx Pharmaceutical Inc
Vivet Therapeutics SAS
Wilson Disease – Drug Profiles
DG-12P1 – Drug Profile
DPM-1001 – Drug Profile
Gene Therapy for Wilson’s Disease – Drug Profile
Gene Therapy to Activate ATP7B for Wilson Disease – Drug Profile
KBHD-001 – Drug Profile
methanobactin – Drug Profile
Small Molecules for Wilson Disease – Drug Profile
SRD-3308 – Drug Profile
tiomolibdate choline – Drug Profile
UX-701 – Drug Profile
VTX-801 – Drug Profile
Wilson Disease – Drug Profile
Wilson Disease – Dormant Projects
Wilson Disease – Product Development Milestones
Featured News & Press Releases
Jun 23, 2022: ALXN1840 shows rapid and sustained improvement in copper mobilization from tissues, potentially closing treatment gaps for Wilson Disease community
May 23, 2022: DepYmed receives FDA Orphan Drug Designation for Clinical Candidate DPM-1001 for the treatment of Wilson Disease
Aug 27, 2021: Alexion’s drug meets primary goal in Phase III Wilson disease trial
Jun 27, 2018: Progress toward improved Wilson's disease drug
Jun 01, 2018: Wilson Therapeutics to present data from WTX101 Phase 2 extension study at 4th Congress of the European Academy of Neurology
Apr 12, 2018: Promising preliminary long-term data for WTX101 in Wilson Disease presented at EASL Annual Meeting
Mar 28, 2018: Preliminary Long-Term Data For WTX101 In Wilson Disease Accepted As A Late-Breaker Presentation At EASL Annual Meeting
Feb 16, 2018: First patient enrolled in pivotal Phase 3 FOCuS trial evaluating WTX101 for the treatment of Wilson Disease
Dec 14, 2017: WTX101 Granted Fast Track Designation by the U.S. FDA for the Treatment of Wilson Disease
Oct 23, 2017: Wilson Therapeutics reaches agreement with the FDA and EMA to initiate pivotal Phase 3 FOCuS study with WTX101 in Wilson Disease
Oct 20, 2017: Promising Preliminary Long-term Data For WTX101 In Wilson Disease Highlighted at The Liver Meeting
Oct 06, 2017: Phase 2 Clinical Trial Data for WTX101 Published in The Lancet Gastroenterology & Hepatology
Oct 01, 2017: Promising Preliminary Long-term Data from WTX101 Phase 2 Extension Study to be Presented at AASLD Annual Meeting
Jun 08, 2017: Wilson Therapeutics presents Phase 2 data for WTX101 at MDS meeting
Apr 25, 2017: Wilson Therapeutics presents promising neurological Phase 2 data for WTX101 at AAN meeting
Appendix
Methodology
Coverage
Secondary Research
Primary Research
Expert Panel Validation
Contact Us
Disclaimer
List of Tables
Table 1: Number of Products under Development for Wilson Disease, 2022
Table 2: Number of Products under Development by Companies, 2022
Table 3: Products under Development by Companies, 2022
Table 4: Products under Development by Companies, 2022 (Contd..1)
Table 5: Number of Products by Stage and Target, 2022
Table 6: Number of Products by Stage and Mechanism of Action, 2022
Table 7: Number of Products by Stage and Route of Administration, 2022
Table 8: Number of Products by Stage and Molecule Type, 2022
Table 9: Wilson Disease – Pipeline by Alexion Pharmaceuticals Inc, 2022
Table 10: Wilson Disease – Pipeline by ARBORMED Pharmaceuticals Inc, 2022
Table 11: Wilson Disease – Pipeline by Deep Genomics Inc, 2022
Table 12: Wilson Disease – Pipeline by DepYmed Inc, 2022
Table 13: Wilson Disease – Pipeline by Enveda Biosciences Inc, 2022
Table 14: Wilson Disease – Pipeline by Generation Bio Co, 2022
Table 15: Wilson Disease – Pipeline by Krisani Bio Sciences Pvt Ltd, 2022
Table 16: Wilson Disease – Pipeline by LambdaGen Therapeutics, 2022
Table 17: Wilson Disease – Pipeline by Logicbio Therapeutics Inc, 2022
Table 18: Wilson Disease – Pipeline by MeiraGTx Holdings Plc, 2022
Table 19: Wilson Disease – Pipeline by Shanghai Pharmaceuticals Holding Co Ltd, 2022
Table 20: Wilson Disease – Pipeline by Ultragenyx Pharmaceutical Inc, 2022
Table 21: Wilson Disease – Pipeline by Vivet Therapeutics SAS, 2022
Table 22: Wilson Disease – Dormant Projects, 2022
List of Figures
Figure 1: Number of Products under Development for Wilson Disease, 2022
Figure 2: Number of Products under Development by Companies, 2022
Figure 3: Number of Products by Targets, 2022
Figure 4: Number of Products by Stage and Targets, 2022
Figure 5: Number of Products by Mechanism of Actions, 2022
Figure 6: Number of Products by Stage and Mechanism of Actions, 2022
Figure 7: Number of Products by Routes of Administration, 2022
Figure 8: Number of Products by Stage and Routes of Administration, 2022
Figure 9: Number of Products by Molecule Types, 2022
Figure 10: Number of Products by Stage and Molecule Types, 2022

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  • This license is for companies that have one location where they want the report to be accessible by all employees within that physical location.

  • This is the most flexible of the licensing options. Some publishers will allow you to get a license for a preset number of people (typically 5). These licenses are ideal for small work groups.

License options are at the discretion of each publisher. As such, not all licenses indicated above are available for every product. If you are uncertain of the best license for your needs or would like a license that is not proactively available, please contact us and we will be happy to assist.

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