Malignant Glioma - Pipeline Insight, 2018 Market Report; Launched via MarketResearchReports.com

Malignant Glioma - Pipeline Insight, 2018 report offers comprehensive Insight of the pipeline (under development) therapeutics scenario and growth prospects across Malignant Glioma development. The report provides detailed coverage of the pipeline landscape for this mechanism of action, equipped with data from multiple sources with complete pipeline analysis by developmental stage, associated indications, route of administration and molecule type.

Pipeline Products covered across the following Developmental Stages:

• Clinical
• Non-clinical
• Inactive: Discontinued and/or Dormant

Descriptive coverage of pipeline development activities for Malignant Glioma

Pipeline therapeutics development coverage provides descriptive product profiles including (but not limited to) drug description, product development and R&D activities encompassing clinical and pre-clinical studies, designations, collaborations, licensing deals, grants, technologies and patent details.

Pipeline Therapeutics assessment of products for Malignant Glioma

The report assesses the active Malignant Glioma pipeline products by developmental stage, product type, molecule type, and administration route.

Methodology

Data used in the report are sourced primarily from internal databases, primary and secondary research and in-house analysis by Publisher’s team of industry experts.

Information and data from the secondary sources have been obtained from various printable and non-printable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.

Scope of the report

• The report provides a snapshot of the pipeline development for the Malignant Glioma
• The report covers pipeline activity across the complete product development cycle i.e. clinical, pre-clinical and discovery stages for the Malignant Glioma
• The report provides pipeline product profiles which includes product description, developmental activities, licensors & collaborators and chemical information
• Provides pipeline assessment by monotherapy and combination therapy products, stage of development, route of administration, and molecule type for Malignant Glioma
• The report also covers the dormant and discontinued pipeline projects related to the Malignant Glioma

Reasons to Buy

• Establish comprehensive understanding of the pipeline activity across this Malignant Glioma to formulate effective R&D strategies
• Gather information of the emerging competitors having potentially lucrative portfolio in this space and create effective counter strategies to gain competitive advantage
• Identify the relationship between the drugs and use it for target finding, drug repurposing, and precision medicine
• Plot corrective measures for pipeline projects by understanding the pipeline depth and focus of Malignant Glioma therapeutics
• Devise in licensing and out licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope
• Modify the therapeutic portfolio by identifying inactive projects and understanding the factors that might have halted their progress

Spanning over 50 pages “Malignant Glioma - Pipeline Insight, 2018” report covers Report Introduction, Malignant Glioma Overview, Pipeline Therapeutics, Comparative Analysis, Products in Clinical Stage, Products in Pre-Clinical and Discovery Stage, Therapeutic Assessment, Inactive Products, Appendix. This report Covered Companies - Advantagene, Amgen Inc., AstraZeneca Plc, BBB Therapeutics B.V., Eisai Co., Eli Lilly and Company, Genmab A/S, Lipopharma Therapeutics SL, MediGene AG, Nuo Therapeutics, Pfizer Inc., Stemline Therapeutics, Tiziana Life Sciences Plc, Vicus Therapeutics, ZIOPHARM Oncology, & list continues.

Please visit this link for more details: http://mrr.cm/Un7

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Overactive Bladder - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Overactive Bladder - Pipeline Review, H1 2018, provides an overview of the Overactive Bladder (Genito Urinary System And Sex Hormones) pipeline landscape.

Overactive bladder is a problem with bladder-storage function that causes a sudden urge to urinate. The urge may be difficult to stop, and overactive bladder may lead to the involuntary loss of urine (incontinence). Symptoms include feel a sudden urge to urinate that's difficult to control, experience urge incontinence and awaken two or more times in the night to urinate. Treatment includes change in life style and medications that relax the bladder can be effective for relieving symptoms of overactive bladder and reducing episodes of urge incontinence.

Report Highlights

Overactive Bladder - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Overactive Bladder (Genito Urinary System And Sex Hormones), 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 Overactive Bladder (Genito Urinary System And Sex Hormones) pipeline guide also reviews of key players involved in therapeutic development for Overactive Bladder 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, Preclinical and Unknown stages are 3, 5, 6, 6, 2, 10 and 3 respectively. Similarly, the Universities portfolio in Preclinical stages comprises 1 molecules, respectively.

Overactive Bladder (Genito Urinary System And Sex Hormones) 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Overactive Bladder (Genito Urinary System And Sex Hormones).
• The pipeline guide reviews pipeline therapeutics for Overactive Bladder (Genito Urinary System And Sex Hormones) 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 Overactive Bladder (Genito Urinary System And Sex Hormones) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Overactive Bladder (Genito Urinary System And Sex Hormones) 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 Overactive Bladder (Genito Urinary System And Sex Hormones)

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 Overactive Bladder (Genito Urinary System And Sex Hormones).
• 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 Overactive Bladder (Genito Urinary System And Sex Hormones) 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.

Spanning over 110 pages “Overactive Bladder - Pipeline Review, H1 2018” report covers Introduction, Report Coverage, Overactive Bladder - Overview, Overactive Bladder - Therapeutics Development, Overactive Bladder - Therapeutics Assessment, Overactive Bladder - Companies Involved in Therapeutics Development, Overactive Bladder - Drug Profiles, Overactive Bladder - Dormant Projects, Appendix. This report Covered Companies few are - Astellas Pharma Inc, Dompe Farmaceutici SpA, Dong-A ST Co Ltd, FemmePharma Global Healthcare Inc, Hanmi Pharmaceuticals Co Ltd, Hydra Biosciences Inc, Ion Channel Innovations LLC, Ipsen SA, Juniper Pharmaceuticals Inc, Kissei Pharmaceutical Co Ltd, Kyorin Pharmaceutical Co Ltd, Lipella Pharmaceuticals Inc.

Please visit this link for more details: http://mrr.cm/Uun

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Polycystic Kidney Disease - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Polycystic Kidney Disease - Pipeline Review, H1 2018, provides an overview of the Polycystic Kidney Disease (Genetic Disorders) pipeline landscape.

Polycystic kidney disease (PKD) is a disorder in which clusters of cysts develop primarily within kidneys. Polycystic kidney disease symptoms may include high blood pressure, back or side pain, headache, blood in urine, frequent urination and kidney failure. The predisposing factors include age and family history. Treatment includes antihypertensive drugs and diuretics.

Report Highlights

Polycystic Kidney Disease - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Polycystic Kidney 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 Polycystic Kidney Disease (Genetic Disorders) pipeline guide also reviews of key players involved in therapeutic development for Polycystic Kidney 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, Preclinical and Discovery stages are 1, 1, 3, 4, 10 and 5 respectively. Similarly, the Universities portfolio in Preclinical stages comprises 2 molecules, respectively.

Polycystic Kidney 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Polycystic Kidney Disease (Genetic Disorders).
• The pipeline guide reviews pipeline therapeutics for Polycystic Kidney 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 Polycystic Kidney Disease (Genetic Disorders) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Polycystic Kidney 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 Polycystic Kidney 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 Polycystic Kidney 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 Polycystic Kidney 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.

Spanning over 108 pages “Polycystic Kidney Disease - Pipeline Review, H1 2018” report covers Introduction, Report Coverage, Polycystic Kidney Disease - Overview, Polycystic Kidney Disease - Therapeutics Development, Polycystic Kidney Disease - Therapeutics Assessment, Polycystic Kidney Disease - Companies Involved in Therapeutics Development, Polycystic Kidney Disease - Drug Profiles, Polycystic Kidney Disease - Dormant Projects, Appendix. This report Covered Companies - Angion Biomedica Corp, Celgene Corp, Conatus Pharmaceuticals Inc, DiscoveryBiomed Inc, Endocyte Inc, Genzyme Corp, IC-MedTech Inc, Ipsen SA, Kadmon Corp LLC, ManRos Therapeutics, Metabolic Solutions Development Company LLC, Mironid Ltd, NovaTarg Therapeutics Inc, Otsuka Holdings Co Ltd, Q BioMed Inc, Reata Pharmaceuticals Inc, Regulus Therapeutics Inc.

Please visit this link for more details: http://mrr.cm/UuP

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Idiopathic Pulmonary Fibrosis - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Idiopathic Pulmonary Fibrosis - Pipeline Review, H1 2018, provides an overview of the Idiopathic Pulmonary Fibrosis (Respiratory) pipeline landscape.

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal disease characterized by inflammation and scarring of lung tissue and loss of lung function. Symptoms of IPF include dry cough, shortness of breath, especially during or after physical activity, lasting tiredness and weight loss. Risk factors include smoking, environmental exposure, viral infections, family history and abnormal acid reflux. Treatment includes antioxidants, biological response modulators, anti-fibrotic agents and anticoagulants.

Report Highlights

Idiopathic Pulmonary Fibrosis - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Idiopathic Pulmonary Fibrosis (Respiratory), 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 Idiopathic Pulmonary Fibrosis (Respiratory) pipeline guide also reviews of key players involved in therapeutic development for Idiopathic Pulmonary Fibrosis 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, Phase I, IND/CTA Filed, Preclinical and Discovery stages are 1, 15, 17, 1, 67 and 12 respectively. Similarly, the Universities portfolio in Preclinical and Discovery stages comprises 3 and 3 molecules, respectively.

Idiopathic Pulmonary Fibrosis (Respiratory) 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Idiopathic Pulmonary Fibrosis (Respiratory).
• The pipeline guide reviews pipeline therapeutics for Idiopathic Pulmonary Fibrosis (Respiratory) 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 Idiopathic Pulmonary Fibrosis (Respiratory) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Idiopathic Pulmonary Fibrosis (Respiratory) 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 Idiopathic Pulmonary Fibrosis (Respiratory)

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 Idiopathic Pulmonary Fibrosis (Respiratory).
• 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 Idiopathic Pulmonary Fibrosis (Respiratory) 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.

Spanning over 302 pages “Idiopathic Pulmonary Fibrosis - Pipeline Review, H1 2018” report covers Introduction, Idiopathic Pulmonary Fibrosis - Overview, Idiopathic Pulmonary Fibrosis - Therapeutics Development, Idiopathic Pulmonary Fibrosis - Therapeutics Assessment, Idiopathic Pulmonary Fibrosis - Companies Involved in Therapeutics Development, Idiopathic Pulmonary Fibrosis - Drug Profiles, Idiopathic Pulmonary Fibrosis - Dormant Projects, Appendix. This report Covered Companies few are - AnaMar AB, apceth Biopharma GmbH, Asahi Kasei Corp, BerGenBio ASA, Biogen Inc, Bioneer Corp, Boehringer Ingelheim GmbH, BreStem Therapeutics Inc, Bristol-Myers Squibb Co, Celgene Corp, Chiesi Farmaceutici SpA.

Please visit this link for more details: http://mrr.cm/Uuf

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Peritoneal Cancer - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Peritoneal Cancer - Pipeline Review, H1 2018, provides an overview of the Peritoneal Cancer (Oncology) pipeline landscape.

Peritoneal cancer is a rare cancer that develops in the peritoneum, a thin, delicate sheet that lines the inside wall of the abdomen and covers the uterus and extends over the bladder and rectum. Peritoneal cancer usually manifests with abdominal distention and diffuse nonspecific abdominal pain secondary to ascites. Peritoneal cancer symptoms may include shortness of breath, rectal bleeding, loss of appetite, frequent urination, constipation, nausea or diarrhea and feeling of fullness, even after a light meal. Treatment includes options such as chemotherapy, surgery, biological therapy and radiation therapy.

Report Highlights

Peritoneal Cancer - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Peritoneal Cancer (Oncology), 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 Peritoneal Cancer (Oncology) pipeline guide also reviews of key players involved in therapeutic development for Peritoneal Cancer and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Pre-Registration, Filing rejected/Withdrawn, Phase III, Phase II, Phase I, Preclinical, Discovery and Unknown stages are 2, 2, 12, 66, 44, 15, 2 and 1 respectively. Similarly, the Universities portfolio in Phase II and Phase I stages comprises 3 and 7 molecules, respectively.

Peritoneal Cancer (Oncology) 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Peritoneal Cancer (Oncology).
• The pipeline guide reviews pipeline therapeutics for Peritoneal Cancer (Oncology) 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 Peritoneal Cancer (Oncology) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Peritoneal Cancer (Oncology) 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 Peritoneal Cancer (Oncology)

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 Peritoneal Cancer (Oncology).
• 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 Peritoneal Cancer (Oncology) 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.

Spanning over 1000 pages “Peritoneal Cancer - Pipeline Review, H1 2018” report covers Introduction, Peritoneal Cancer - Overview, Peritoneal Cancer - Therapeutics Development, Peritoneal Cancer - Therapeutics Assessment, Peritoneal Cancer - Companies Involved in Therapeutics Development, Peritoneal Cancer - Drug Profiles, Peritoneal Cancer - Dormant Projects, Appendix. This report Covered Companies few are - Atara Biotherapeutics Inc, AVEO Pharmaceuticals Inc, Bayer AG, BeiGene Ltd, Boehringer Ingelheim GmbH, Boston Biomedical Inc, Bristol-Myers Squibb Co, Caladrius Biosciences Inc, Dr. Reddy's Laboratories Ltd, Eisai Co Ltd, F. Hoffmann-La Roche Ltd, Fate Therapeutics Inc, Gene Techno Science Co Ltd.

Please visit this link for more details: http://mrr.cm/UuX

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Primary Biliary Cirrhosis - Pipeline Insight, 2018 Market Report; Launched via MarketResearchReports.com

Primary Biliary Cirrhosis - Pipeline Insight, 2018 report offers comprehensive Insight of the pipeline (under development) therapeutics scenario and growth prospects across Primary Biliary Cirrhosis development. The report provides detailed coverage of the pipeline landscape for this mechanism of action, equipped with data from multiple sources with complete pipeline analysis by developmental stage, associated indications, route of administration and molecule type.

Pipeline Products covered across the following Developmental Stages:

• Clinical
• Non-clinical
• Inactive: Discontinued and/or Dormant

Descriptive coverage of pipeline development activities for Primary Biliary Cirrhosis

Pipeline therapeutics development coverage provides descriptive product profiles including (but not limited to) drug description, product development and R&D activities encompassing clinical and pre-clinical studies, designations, collaborations, licensing deals, grants, technologies and patent details.

Pipeline Therapeutics assessment of products for Primary Biliary Cirrhosis

The report assesses the active Primary Biliary Cirrhosis pipeline products by developmental stage, product type, molecule type, and administration route.

Methodology

Data used in the report are sourced primarily from internal databases, primary and secondary research and in-house analysis by Publisher’s team of industry experts.

Information and data from the secondary sources have been obtained from various printable and non-printable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.

Scope of the report

• The report provides a snapshot of the pipeline development for the Primary Biliary Cirrhosis
• The report covers pipeline activity across the complete product development cycle i.e. clinical, pre-clinical and discovery stages for the Primary Biliary Cirrhosis
• The report provides pipeline product profiles which includes product description, developmental activities, licensors & collaborators and chemical information
• Provides pipeline assessment by monotherapy and combination therapy products, stage of development, route of administration, and molecule type for Primary Biliary Cirrhosis
• The report also covers the dormant and discontinued pipeline projects related to the Primary Biliary Cirrhosis

Reasons to Buy

• Establish comprehensive understanding of the pipeline activity across this Primary Biliary Cirrhosis to formulate effective R&D strategies
• Gather information of the emerging competitors having potentially lucrative portfolio in this space and create effective counter strategies to gain competitive advantage
• Identify the relationship between the drugs and use it for target finding, drug repurposing, and precision medicine
• Plot corrective measures for pipeline projects by understanding the pipeline depth and focus of Primary Biliary Cirrhosis therapeutics
• Devise in licensing and out licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope
• Modify the therapeutic portfolio by identifying inactive projects and understanding the factors that might have halted their progress

Spanning over 50 pages “Primary Biliary Cirrhosis - Pipeline Insight, 2018” report covers Report Introduction, Primary Biliary Cirrhosis Overview, Pipeline Therapeutics, Comparative Analysis, Products in Clinical Stage, Products in Pre-Clinical and Discovery Stage, Therapeutic Assessment, Inactive Products, Appendix. This report Covered Companies - Albireo Pharma Inc, Arena Pharmaceuticals Inc, CymaBay Therapeutics Inc, Eisai Co Ltd, Enanta Pharmaceuticals Inc, Genfit SA, GenKyoTex SA, Gilead Sciences Inc, GlaxoSmithKline Plc, Intercept Pharmaceuticals Inc, MediGene AG, NGM Biopharmaceuticals Inc, Novartis AG, Retrophin Inc, Shire Plc, & list continues.

Please visit this link for more details: http://mrr.cm/UBn

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Radiation Injury - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Radiation Injury - Pipeline Review, H1 2018, provides an overview of the Radiation Injury (Toxicology) pipeline landscape.

Radiation injury is damage to tissues caused by exposure to ionizing radiation. Symptoms depend on whether radiation exposure involves the whole body or is limited to a small portion of the body. At high doses, whole-body exposure causes acute radiation illness, and partial-body exposure causes local radiation injury.

Report Highlights

Radiation Injury - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Radiation Injury (Toxicology), 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 Radiation Injury (Toxicology) pipeline guide also reviews of key players involved in therapeutic development for Radiation Injury and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Phase III, IND/CTA Filed, Preclinical, Discovery and Unknown stages are 1, 1, 7, 2 and 1 respectively. Similarly, the Universities portfolio in Preclinical stages comprises 1 molecules, respectively.

Radiation Injury (Toxicology) 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Radiation Injury (Toxicology).
• The pipeline guide reviews pipeline therapeutics for Radiation Injury (Toxicology) 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 Radiation Injury (Toxicology) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Radiation Injury (Toxicology) 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 Radiation Injury (Toxicology)

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 Radiation Injury (Toxicology).
• 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 Radiation Injury (Toxicology) 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.

Spanning over 46 pages “Radiation Injury - Pipeline Review, H1 2018” report covers Introduction, Report Coverage, Radiation Injury - Overview, Radiation Injury - Therapeutics Development, Radiation Injury - Therapeutics Assessment, Radiation Injury - Companies Involved in Therapeutics Development, Radiation Injury - Drug Profiles, Radiation Injury - Dormant Projects, Appendix. This report Covered Companies - FirstString Research Inc, PharmaIN Corp, Synedgen Inc, Tonix Pharmaceuticals Holding Corp, Windtree Therapeutics Inc.

Please visit this link for more details: http://mrr.cm/UuM

Find all Pharma and Healthcare Reports at: http://www.marketresearchreports.com/pharma-healthcare

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Global Surgical Bone Drill Industry 2018 Market Report; Launched via MarketResearchReports.com

In this report, we analyze the Surgical Bone Drill industry from two aspects. One part is about its production and the other part is about its consumption. In terms of its production, we analyze the production, revenue, gross margin of its main manufacturers and the unit price that they offer in different regions from 2013 to 2018. In terms of its consumption, we analyze the consumption volume, consumption value, sale price, import and export in different regions from 2013 to 2018. We also make a prediction of its production and consumption in coming 2018-2023.

At the same time, we classify different Surgical Bone Drill based on their definitions. Upstream raw materials, equipment and downstream consumers analysis is also carried out. What is more, the Surgical Bone Drill industry development trends and marketing channels are analyzed.

Finally, the feasibility of new investment projects is assessed, and overall research conclusions are offered.

Key players in global Surgical Bone Drill market include:

• Adeor
• Allotech
• Arthrex
• BIOTECH DENTAL
• ConMed
• DENTATUS AB
• DENTSPLY MAILLEFER
• Depuy Synthes
• DeSoutter Medical
• MedicMicro

Market segmentation, by product types:

• Electric Bone Drill
• Manual Bone Drill

Market segmentation, by applications:

• Arthroscopic Surgery
• ENT Surgery
• Bone Corrective Surgery

Market segmentation, by regions:

• North America
• Europe
• Asia Pacific
• Middle East & Africa
• Latin America

The report can answer the following questions:

1. What is the global (North America, South America, Europe, Africa, Middle East, Asia, China, Japan) production, production value, consumption, consumption value, import and export of Surgical Bone Drill?

2. Who are the global key manufacturers of Surgical Bone Drill industry? How are their operating situation (capacity, production, price, cost, gross and revenue)?

3. What are the types and applications of Surgical Bone Drill? What is the market share of each type and application?

4. What are the upstream raw materials and manufacturing equipment of Surgical Bone Drill? What is the manufacturing process of Surgical Bone Drill?

5. Economic impact on Surgical Bone Drill industry and development trend of Surgical Bone Drill industry.

6. What will the Surgical Bone Drill market size and the growth rate be in 2023?

7. What are the key factors driving the global Surgical Bone Drill industry?

8. What are the key market trends impacting the growth of the Surgical Bone Drill market?

9. What are the Surgical Bone Drill market challenges to market growth?

10. What are the Surgical Bone Drill market opportunities and threats faced by the vendors in the global Surgical Bone Drill market?

Objective of Studies:

1. To provide detailed analysis of the market structure along with forecast of the various segments and sub-segments of the global Surgical Bone Drill market.

2. To provide insights about factors affecting the market growth. To analyze the Surgical Bone Drill market based on various factors- price analysis, supply chain analysis, Porte five force analysis etc.

3. To provide historical and forecast revenue of the market segments and sub-segments with respect to four main geographies and their countries- North America, Europe, Asia, Latin America and Rest of the World.

4. To provide country level analysis of the market with respect to the current market size and future prospective.

5. To provide country level analysis of the market for segment by application, product type and sub-segments.

6. To provide strategic profiling of key players in the market, comprehensively analyzing their core competencies, and drawing a competitive landscape for the market.

7. To track and analyze competitive developments such as joint ventures, strategic alliances, mergers and acquisitions, new product developments, and research and developments in the global Surgical Bone Drill market.

Spanning over 150 pages “Global Surgical Bone Drill Industry Market Research 2018” report covers Industry Overview of Surgical Bone Drill, Industry Chain Analysis of Surgical Bone Drill, Manufacturing Technology of Surgical Bone Drill, Major Manufacturers Analysis of Surgical Bone Drill, Global Productions, Revenue and Price Analysis of Surgical Bone Drill by Regions, Manufacturers, Types and Applications, Global and Major Regions Capacity, Production, Revenue and Growth Rate of Surgical Bone Drill 2013-2018, Consumption Volumes, Consumption Value, Import, Export and Sale Price Analysis of Surgical Bone Drill by Regions, Gross and Gross Margin Analysis of Surgical Bone Drill, Marketing Traders or Distributor Analysis of Surgical Bone Drill, Global and Chinese Economic Impacts on Surgical Bone Drill Industry, Development Trend Analysis of Surgical Bone Drill, Contact information of Surgical Bone Drill, New Project Investment Feasibility Analysis of Surgical Bone Drill, Conclusion of the Global Surgical Bone Drill Industry 2018 Market Research Report.

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For related reports please visit: Surgical Bone Drill Market Research Reports

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Heavy Metal Poisoning - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Heavy Metal Poisoning - Pipeline Review, H1 2018, provides an overview of the Heavy Metal Poisoning (Toxicology) pipeline landscape.

Heavy metal poisoning is the accumulation of heavy metals, in toxic amounts, in the soft tissues of the body. Sources of toxicity can include environmental, water supply, industrial and hobbies. Symptoms include headaches, drowsiness, confusion, seizures, nausea, vomiting, abdominal cramps, tinnitus, goiter, anorexia and diarrhea. Treatment includes chelation therapy.

Report Highlights

Heavy Metal Poisoning - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Heavy Metal Poisoning (Toxicology), 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 Heavy Metal Poisoning (Toxicology) pipeline guide also reviews of key players involved in therapeutic development for Heavy Metal Poisoning and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Phase II, Phase I and Preclinical stages are 1, 2 and 4 respectively. Similarly, the Universities portfolio in IND/CTA Filed, Preclinical and Discovery stages comprises 1, 1 and 1 molecules, respectively.

Heavy Metal Poisoning (Toxicology) 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Heavy Metal Poisoning (Toxicology).
• The pipeline guide reviews pipeline therapeutics for Heavy Metal Poisoning (Toxicology) 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 Heavy Metal Poisoning (Toxicology) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Heavy Metal Poisoning (Toxicology) 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 Heavy Metal Poisoning (Toxicology)

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 Heavy Metal Poisoning (Toxicology).
• 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 Heavy Metal Poisoning (Toxicology) 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.

Spanning over 40 pages “Heavy Metal Poisoning - Pipeline Review, H1 2018” report covers Introduction, Report Coverage, Heavy Metal Poisoning - Overview, Heavy Metal Poisoning - Therapeutics Development, Heavy Metal Poisoning - Therapeutics Assessment, Heavy Metal Poisoning - Companies Involved in Therapeutics Development, Heavy Metal Poisoning - Drug Profiles, Heavy Metal Poisoning - Dormant Projects, Appendix. This report Covered Companies - La Jolla Pharmaceutical Company, Medesis Pharma SA, PDX Pharmaceuticals LLC.

Please visit this link for more details: http://mrr.cm/Uue

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Gastric Cancer - Pipeline Review, H1 2018 Market Report; Launched via MarketResearchReports.com

Gastric Cancer - Pipeline Review, H1 2018, provides an overview of the Gastric Cancer (Oncology) pipeline landscape.

Gastric cancer, also called stomach cancer, is a malignant tumor arising from the lining of the stomach. Signs and symptoms of gastric cancer include fatigue, stomach pain, vomiting, weight loss that is unintentional, feeling bloated after eating, heartburn and indigestion. Risk factors include smoking, pernicious anemia, stomach polyps, infection with helicobacter pylori and family history of stomach cancer. Treatment includes surgery, chemotherapy and radiation therapy.

Report Highlights

Gastric Cancer - Pipeline Review, H1 2018, provides comprehensive information on the therapeutics under development for Gastric Cancer (Oncology), 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 Gastric Cancer (Oncology) pipeline guide also reviews of key players involved in therapeutic development for Gastric Cancer and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Pre-Registration, Filing rejected/Withdrawn, Phase III, Phase II, Phase I, IND/CTA Filed, Preclinical, Discovery and Unknown stages are 3, 2, 14, 80, 99, 11, 97, 17 and 5 respectively. Similarly, the Universities portfolio in Phase II, Phase I, IND/CTA Filed, Preclinical and Discovery stages comprises 9, 3, 1, 9 and 2 molecules, respectively.

Gastric Cancer (Oncology) 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 Publisher’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.

Scope

• The pipeline guide provides a snapshot of the global therapeutic landscape of Gastric Cancer (Oncology).
• The pipeline guide reviews pipeline therapeutics for Gastric Cancer (Oncology) 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 Gastric Cancer (Oncology) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Gastric Cancer (Oncology) 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 Gastric Cancer (Oncology)

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 Gastric Cancer (Oncology).
• 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 Gastric Cancer (Oncology) 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.

Spanning over 1283 pages “Gastric Cancer - Pipeline Review, H1 2018” report covers Introduction, Gastric Cancer - Overview, Gastric Cancer - Therapeutics Development, Gastric Cancer - Therapeutics Assessment, Gastric Cancer - Companies Involved in Therapeutics Development, Gastric Cancer - Drug Profiles, Gastric Cancer - Dormant Projects, Appendix. This report Covered Companies few are - Aurigene Discovery Technologies Ltd, Avipep Pty Ltd, Basilea Pharmaceutica Ltd, Bayer AG, BeiGene Ltd, CSPC Pharmaceutical Group Limited, Curaxys SL, Cytori Therapeutics Inc, Daiichi Sankyo Co Ltd, Exelixis Inc, F-star Biotechnology Ltd, F. Hoffmann-La Roche Ltd.

Please visit this link for more details: http://mrr.cm/Uu6

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