"Autosomal Dominant Polycystic Kidney Disease Pipeline Insight, 2020" report by DelveInsight outlays comprehensive insights of present clinical development scenario and growth prospects across the Autosomal Dominant Polycystic Kidney Disease market. A detailed picture of the Autosomal Dominant Polycystic Kidney Disease pipeline landscape is provided, which includes the disease overview and Autosomal Dominant Polycystic Kidney Disease treatment guidelines. The assessment part of the report embraces in-depth Autosomal Dominant Polycystic Kidney Disease commercial assessment and clinical assessment of the Autosomal Dominant Polycystic Kidney Disease pipeline products from the pre-clinical developmental phase to the marketed phase. In the report, a detailed description of the drug is proffered including mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, Autosomal Dominant Polycystic Kidney Disease collaborations, licensing, mergers and acquisition, funding, designations, and other product-related details.
The report provides insights into:
The report is built using data and information traced from the researcher's proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university web sites and industry-specific third-party sources, etc.
This report provides a comprehensive commercial assessment of therapeutic drugs that have been included, which comprises of collaborations, licensing, and acquisition deal value trends. The report also covers company-company collaborations (licensing/partnering), company-academia collaborations, and acquisition analysis in both graphical and tabulated form in a detailed manner.
The report comprises of comparative clinical assessment of products by development stage, product type, route of administration, molecule type, and MOA type across this indication.
1. Report Introduction
2. Autosomal Dominant Polycystic Kidney Disease
2.1. Overview
2.2. History
2.3. Autosomal Dominant Polycystic Kidney Disease Symptoms
2.4. Causes
2.5.Pathophysiology
2.6. Autosomal Dominant Polycystic Kidney Disease Diagnosis
2.6.1. Diagnostic Guidelines
3. Autosomal Dominant Polycystic Kidney Disease Current Treatment Patterns
3.1. Autosomal Dominant Polycystic Kidney Disease Treatment Guidelines
4. Autosomal Dominant Polycystic Kidney Disease - DelveInsight's Analytical Perspective
4.1. In-depth Commercial Assessment
4.1.1. Autosomal Dominant Polycystic Kidney Disease companies collaborations, Licensing, Acquisition -Deal Value Trends
4.1.1.1. Assessment Summary
4.1.2. Autosomal Dominant Polycystic Kidney Disease Collaboration Deals
4.1.2.1. Company-Company Collaborations (Licensing / Partnering) Analysis
4.1.2.2. Company-University Collaborations (Licensing / Partnering) Analysis
4.1.2.3. Autosomal Dominant Polycystic Kidney Disease Acquisition Analysis
5. Therapeutic Assessment
5.1. Clinical Assessment of Pipeline Drugs
5.1.1. Assessment by Phase of Development
5.1.2. Assessment by Product Type (Mono / Combination)
5.1.2.1. Assessment by Stage and Product Type
5.1.3. Assessment by Route of Administration
5.1.3.1. Assessment by Stage and Route of Administration
5.1.4. Assessment by Molecule Type
5.1.4.1. Assessment by Stage and Molecule Type
5.1.5. Assessment by MOA
5.1.5.1. Assessment by Stage and MOA
5.1.6. Assessment by Target
5.1.6.1. Assessment by Stage and Target
6. Autosomal Dominant Polycystic Kidney Disease Late Stage Products (Phase-III)
7. Autosomal Dominant Polycystic Kidney Disease Mid Stage Products (Phase-II)
8. Early Stage Products (Phase-I)
9. Pre-clinical Products and Discovery Stage Products
10. Inactive Products
11. Dormant Products
12. Autosomal Dominant Polycystic Kidney Disease Discontinued Products
13. Autosomal Dominant Polycystic Kidney Disease Product Profiles
13.1. Drug Name: Company
13.1.1. Product Description
13.1.1.1. Product Overview
13.1.1.2. Mechanism of action
13.1.2. Research and Development
13.1.2.1. Clinical Studies
13.1.3. Product Development Activities
13.1.3.1. Collaboration
13.1.3.2. Agreements
13.1.3.3. Acquisition
13.1.3.4. Patent Detail
13.1.4. Tabulated Product Summary
13.1.4.1. General Description Table
Detailed information in the report?
14. Autosomal Dominant Polycystic Kidney Disease Key Companies
15. Autosomal Dominant Polycystic Kidney Disease Key Products
16. Dormant and Discontinued Products
16.1. Dormant Products
16.1.1. Reasons for being dormant
16.2. Discontinued Products
16.2.1. Reasons for the discontinuation
17. Autosomal Dominant Polycystic Kidney Disease Unmet Needs
18. Autosomal Dominant Polycystic Kidney Disease Future Perspectives
19. Autosomal Dominant Polycystic Kidney Disease Analyst Review
20. Appendix
21. Report Methodology
21.1. Secondary Research
21.2. Expert Panel Validation
Table 1: Autosomal Dominant Polycystic Kidney Disease Diagnostic Guidelines
Table 2: Autosomal Dominant Polycystic Kidney Disease Treatment Guidelines
Table 3: Assessment Summary
Table 4: Company-Company Collaborations (Licensing / Partnering) Analysis
Table 5: Autosomal Dominant Polycystic Kidney Disease Acquisition Analysis
Table 6: Assessment by Phase of Development
Table 7: Assessment by Product Type (Mono / Combination)
Table 8: Assessment by Stage and Product Type
Table 9: Assessment by Route of Administration
Table 10: Assessment by Stage and Route of Administration
Table 11: Assessment by Molecule Type
Table 12: Assessment by Stage and Molecule Type
Table 13: Assessment by MOA
Table 14: Assessment by Stage and MOA
Table 15: Assessment by Target
Table 16: Assessment by Stage and Target
Table 17: Autosomal Dominant Polycystic Kidney Disease Late Stage Products (Phase-III)
Table 18: Autosomal Dominant Polycystic Kidney Disease Mid Stage Products (Phase-II)
Table 19: Autosomal Dominant Polycystic Kidney Disease Early Stage Products (Phase-I)
Table 20: Pre-clinical and Discovery Stage Products
Table 21: Inactive Products
Table 22: Dormant Products
Table 23: Discontinued Products
Figure 1: Disease Overview
Figure 2: History
Figure 3: Symptoms
Figure 4: Causes
Figure 5: Pathophysiology
Figure 6: Diagnostic Guidelines
Figure 7: Treatment Guidelines
Figure 8: Autosomal Dominant Polycystic Kidney Disease companies collaborations, Licensing, Acquisition -Deal Value Trends
Figure 9: Company-Company Collaborations (Licensing / Partnering) Analysis
Figure 10: Autosomal Dominant Polycystic Kidney Disease Acquisition Analysis
Figure 11: Assessment by Phase of Development
Figure 12: Assessment by Product Type (Mono / Combination)
Figure 13: Assessment by Stage and Product Type
Figure 14: Assessment by Route of Administration
Figure 15: Assessment by Stage and Route of Administration
Figure 16: Assessment by Molecule Type
Figure 17: Assessment by Stage and Molecule Type
Figure 18: Assessment by MOA
Figure 19: Assessment by Stage and MOA
Figure 20: Late Stage Products (Phase-III)
Figure 21: Mid Stage Products (Phase-II)
Figure 22: Early Stage Products (Phase-I)
Figure 23: Pre-clinical and Discovery Stage Products
Figure 24: Inactive Products
Figure 25: Dormant Products
Figure 26: Discontinued Products
Figure 27: Unmet Needs
