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1. Introduction
1.1. Report Overview
2. Neuroendocrine
Tumours - Overview
3. Executive Summary
4. Neuroendocrine
Tumours : Pipeline Assessment
4.1. By Stage of Development
4.2. By Route of Administration
4.3. By Drug Class
4.4. By Molecule Type
4.5. By Therapy Area / Indication
4.6. By Drug Target
4.7. By Sponsor
5. Neuroendocrine
Tumours: Company & Drug Profiles
5.1. Clinical Stage
5.1.1. Sulfatinib
β Hutchison Medipharma Limited.
5.1.1.1.
Company Overview
5.1.1.2.
Product Description
5.1.1.3.
R&D Status & Development Activities
5.1.1.4.
Mechanism of Action
5.1.1.5.
Molecule Type
5.1.1.6. Stage
of Development
5.1.1.7.
Indications
5.1.1.8. Route
of Administration
5.1.1.9.
Funding
5.1.2.
XmAb18087 β Xencor, Inc.
5.1.2.1.
Company Overview
5.1.2.2.
Product Description
5.1.2.3.
R&D Status & Development Activities
5.1.2.4.
Mechanism of Action
5.1.2.5.
Molecule Type
5.1.2.6. Stage
of Development
5.1.2.7.
Indications
5.1.2.8. Route
of Administration
5.1.2.9.
Funding
5.1.3.
Humanized anti-PD-1 monoclonal antibody β Shanghai Junshi Biosciencee Co.
5.1.3.1.
Company Overview
5.1.3.2.
Product Description
5.1.3.3.
R&D Status & Development Activities
5.1.3.4.
Mechanism of Action
5.1.3.5.
Molecule Type
5.1.3.6. Stage
of Development
5.1.3.7.
Indications
5.1.3.8. Route
of Administration
5.1.3.9.
Funding
5.1.4. Others
5.2. Preclinical
5.2.1. Company
Overview
5.2.2. Product
Description
5.2.3. R&D
Status & Development Activities
5.2.4.
Mechanism of Action
5.2.5.
Molecule Type
5.2.6.
Indications
5.2.7. Route
of Administration
5.2.8. Funding
6. Neuroendocrine
Tumours: An Overview on Dormant & Discontinued Pipeline Candidates
6.1. Overview
6.2. Product Description
6.3. Reason for Discontinuation
7. Neuroendocrine
Tumours: Additional Key Insights
7.1. Epidemiology Overview:
Neuroendocrine Tumours
7.2. Current Market Scenario:
Neuroendocrine Tumours Therapeutics
8. Neuroendocrine Tumours: News, Press Releases and Conference Details
Note:
1) This Table of Content is tentative and subject to change as the research progresses.
2) Please note that the drug candidates included as examples were in the pipeline when this TOC was designed and their status might have changed since then.
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