PharmSource: Contract Manufacturing of Novel In-Licensed Drugs 2020 – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “PharmSource: Contract Manufacturing of Novel In-Licensed Drugs – 2020 Edition” report has been added to ResearchAndMarkets.com’s offering.

This expert trend report explores in-licensing trends among FDA New Molecule Entity (NME) approvals 2014-2018, and analyzes how licensing patterns affect the propensity to outsource finished dose manufacture. This report is critical for establishing an understanding of the ways bio/pharmaceutical companies source their drugs, and the factors that make them more likely to engage a contract manufacturing organization (CMO).

This report would be of interest to:

• CMO executives who must have a deep understanding of the NME approvals landscape to make strategic planning and investment decisions.
• Sourcing and procurement executives who must understand crucial components of the supply base in order to make decisions about supplier selection and management.
• Pharmaceutical and biotech companies evaluating potential licensing deals as a licensor or licensee.
• Investors that need a deeper understanding of the market to identify and value potential investment targets.

Reasons to Buy

• Overview of novel drugs (NMEs) approved by FDA 2014-2018
• Detailed analysis of dose outsourcing likelihood by: licensing status, market cap, molecule type
• Spotlight on licensing deals and outsourcing propensity
• Detailed methodology explains use of data from the The publisher Pharma Intelligence Center databases

Key Topics Covered:

1 Table of Contents

2 List of Tables

3 List of Figures

4 Executive Summary

5 Introduction

6 Licensing of New Molecular Entities Approved 2014-2018

7 Timing of Licensing Deals

7.1 Chronology of Licensing and Outsourcing

8 Outsourcing Propensity by Source of NME

8.1 Product Source and Outsourcing Propensity by Market Cap

9 Trends by Molecule Type

9.1 In-Licensing by Molecule Type

9.1.1 Spotlight On: Cell and Gene Therapies

9.2 Dose Manufacture by Molecule Type

10 Company Analysis

11 What It Means

12 Notes on Methodology

13 Appendix

List of Tables

Table 1: Breakdown of Approvals 2014-2018 by Company Market Cap Band

List of Figures

Figure 1: Source of NMEs Approved 2014-2018

Figure 2: Source of NMEs Approved 2014-2018, by Year

Figure 3: Status of Approved In-Licensed NMEs at Time of Licensing Deal, 2014-2018

Figure 4: Status of Approved In-Licensed NMEs at Time of Licensing Deal, 2014-2018, by Year

Figure 5: Chronology of Licensing and Outsourcing for NMEs Approved 2014-2018

Figure 6: Source of Dose-Outsourced NMEs (Approved 2014-2018)

Figure 7: Dose Form Manufacture by Source of NMEs Approved 2014-2018

Figure 8: Dose Outsourcing of NMEs (Approved 2014-2018) by Company Market Cap and NME Source

Figure 9: NME Source by Molecule Type

Figure 10: Dose Manufacture of In-licensed NMEs Approved 2014-2018, by Molecule Type

Figure 11: Top 9 Companies by NME Approvals 2014-2018, by NME Source

Companies Mentioned

• Amgen Inc
• Astellas Pharma
• AstraZeneca Plc
• Bristol-Myers Squibb
• Cabaret Biotech
• ClearView Healthcare Partners
• CSL
• Cytovant Sciences
• Eli Lilly and Co
• Gilead Sciences
• GlaxoSmithKline
• Johnson & Johnson
• Legend Biotech

For more information about this report visit https://www.researchandmarkets.com/r/w79toy

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