Hypoparathyroidism - Pipeline Review, H1 2015

02:29 EDT 22 Jul 2015 | BioPortfolio Reports

Recently added to the BioPortfolio report store, Hypoparathyroidism - Pipeline Review, H1 2015 is a new report from Global Markets Direct published on 2015-06-16. This 43-page report is available in PDF from $2000.

Hypoparathyroidism - Pipeline Review, H1 2015


Global Markets Direct’s, ‘Hypoparathyroidism - Pipeline Review, H1 2015’, provides an overview of the Hypoparathyroidism’s therapeutic pipeline.

This report provides comprehensive information on the therapeutic development for Hypoparathyroidism, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Hypoparathyroidism and special features on late-stage and discontinued projects.

Global Markets Direct’s report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from Global Markets Direct’s proprietary databases, Company/University websites, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources, put together by Global Markets Direct’s team. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis.

The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products.

Note*: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease.


- The report provides a snapshot of the global therapeutic landscape of Hypoparathyroidism
- The report reviews key pipeline products under drug profile section which includes, product description, MoA and R&D brief, licensing and collaboration details & other developmental activities
- The report reviews key players involved in the therapeutics development for Hypoparathyroidism and enlists all their major and minor projects
- The report summarizes all the dormant and discontinued pipeline projects
- A review of the Hypoparathyroidism products under development by companies and universities/research institutes based on information derived from company and industry-specific sources
- Pipeline products coverage based on various stages of development ranging from pre-registration till discovery and undisclosed stages
- A detailed assessment of monotherapy and combination therapy pipeline projects
- Coverage of the Hypoparathyroidism pipeline on the basis of target, MoA, route of administration and molecule type
- Latest news and deals relating related to pipeline products

Reasons to buy

- Provides strategically significant competitor information, analysis, and insights to formulate effective R&D development strategies
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage
- Develop strategic initiatives by understanding the focus areas of leading companies
- Identify and understand important and…

Table of Contents
Table of Contents 2
List of Tables 4
List of Figures 4
Introduction 5
Global Markets Direct Report Coverage 5
Hypoparathyroidism Overview 6
Therapeutics Development 7
Pipeline Products for Hypoparathyroidism - Overview 7
Pipeline Products for Hypoparathyroidism - Comparative Analysis 8
Hypoparathyroidism - Therapeutics under Development by Companies 9
Hypoparathyroidism - Pipeline Products Glance 10
Late Stage Products 10
Clinical Stage Products 11
Early Stage Products 12
Hypoparathyroidism - Products under Development by Companies 13
Hypoparathyroidism - Companies Involved in Therapeutics Development 14
Chugai Pharmaceutical Co., Ltd. 14
Rhein-Minapharm Biogenetics SAE 15
Shire Plc 16
Hypoparathyroidism - Therapeutics Assessment 17
Assessment by Monotherapy Products 17
Assessment by Target 18
Assessment by Mechanism of Action 20
Assessment by Route of Administration 22
Assessment by Molecule Type 24
Drug Profiles 26
Eu-232 - Drug Profile 26
Product Description 26
Mechanism of Action 26
R&D Progress 26
parathyroid hormone (recombinant) - Drug Profile 27
Product Description 27
Mechanism of Action 27
R&D Progress 27
PCO-371 - Drug Profile 30
Product Description 30
Mechanism of Action 30
R&D Progress 30
Recombinant Protein to Agonize PTH-R for Hypoparathyroidism - Drug Profile 31
Product Description 31
Mechanism of Action 31
R&D Progress 31
teriparatide - Drug Profile 32
Product Description 32
Mechanism of Action 32
R&D Progress 32
Hypoparathyroidism - Recent Pipeline Updates 33
Hypoparathyroidism - Product Development Milestones 36
Hypoparathyroidism - Product Development Milestones 36
Featured News & Press Releases 36
Jan 23, 2015: FDA approves Natpara to control low blood calcium levels in patients with hypoparathyroidism 36
Dec 02, 2014: European Medicines Agency Validates Marketing Authorization Application for Natpar (parathyroid hormone (rDNA)) in Hypoparathyroidism 37
Oct 23, 2014: PDUFA Action Date For Natpara BLA Extended Three Months To January 24, 2015 37
Sep 12, 2014: FDA Advisory Committee Recommends Approval of Natpara for Long-Term Treatment of Hypoparathyroidism 38
Sep 12, 2014: FDA Advisory Committee to Review Natpara Biologics License Application 38
Sep 10, 2014: FDA Posts Briefing Materials for Advisory Committee Meeting Reviewing Natpara® for Hypoparathyroidism 38
Jul 24, 2014: PARADOX Findings Published in Endocrine Practice Describe High Burden of Illness in Patients with Hypoparathyroidism 39
Jun 10, 2014: NPS Pharma Reports Change in Tentative Date of FDA Advisory Committee Review of Natpara BLA to September 12 - PDUFA Date of October 24 Remains Unchanged 40
Jan 07, 2014: NPS Pharmaceuticals Announces FDA Acceptance of Biologics License Application for Natpara for the Treatment of Hypoparathyroidism 40
Jan 03, 2014: NPS Pharmaceuticals Receives Orphan Drug Designation for Natpara in Europe 41
Appendix 42
Methodology 42
Coverage 42
Secondary Research 42
Primary Research 42
Expert Panel Validation…

For more information open Hypoparathyroidism - Pipeline Review, H1 2015.


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