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KuicK Researchが発行した調査報告書(DATA90502)
◆英語タイトル:US Biosimilars Market , Dosage, Price & Clinical Pipeline Outlook 2025
◆商品コード:DATA90502
◆発行会社(リサーチ会社):KuicK Research
◆発行日:2019年4月
◆ページ数:300
◆レポート形式:英語 / PDF
◆納品方法:Eメール
◆調査対象地域:アメリカ
◆産業分野:医療・製薬
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【レポートの概要】

“US Biosimilars Market, Dosage, Price & Clinical Pipeline Outlook 2025″ Report Highlights:
• US Biosimilar Market Current Scenario
• US Biosimilars Clinical Pipeline by Company, Indication & Phase: 28 Biosimilars
• Marketed Biosimilars Clinical Insight by Company & Indication: 9 Biosimilars
• Biosimilars Market Opportunity: US$ 5 Billion
• FDA Rules & Regulations For Biosimilars Development & Market
• Approved & Marketed Biosimilars: Clinical Insight, Price & Dosage

“US Biosimilars Market, Dosage, Price & Clinical Pipeline Outlook 2025″ report gives comprehensive insight on clinical and non-clinical issues involved in the development of biosimilars market in US. Report highlights the ongoing market trends and initiatives undertaken by various stake holders to advance the approval and commercialization of biosimilars in the US pharmaceutical market.

Biosimilars have started gaining attention worldwide as they are cheaper but equally effective than their original product. Biosimilars cost lesser than biologics as they take less time to develop and go through only four stages of testing – analytical, non-clinical, clinical pharmacology and clinical studies. Biosimilars are not similar or same as generic drugs due to difference in their physiochemical properties.

Globally they are at different stages of progression with respect to adoption of biosimilars in main stream pharmaceutical market. Although European market is the most mature market in comparison to US market but it is catching up to speed. Total of 19 biosimilars have been approved by FDA since 2014, but only 9 biosimilars have been able to make it to the market as of 2019. The most recent approved biosimilar is Trazimera of Pfizer (March 11, 2019).

Most successful biosimilar in the US market has been Sandoz’s Zarxio. It captured more market than Inflectra. Biosimilars market has a bright future. The market has the potential to grow faster if some of the issues like interchangeability status, extrapolation, shortening exclusivity period etc. are solved. In addition, market competition needs to be promoted.

Currently, US biosimilars market is at the interim state. With most of the biologic products going off patent by 2025 and increasing rate of patients suffering from chronic diseases. The biosimilars market has a huge opportunity to spread it swings in the US drug market. With few reforms and education to the stakeholders this goal is achievable. The US biosimilar market will continue to evolve and grow exponentially but with small degree of uncertainty. The regulatory authorities need to form a more concrete framework to keep these grey areas of the biosimilar market in check. This, accompanied with education of physicians/patients to speed market uptake, new development and commercial paradigms can provide the proper platform for developing new commercially successful biosimilars.

【レポートの目次】

1. Overview Of Biosimilars Market
1.1 History & Evolution Of Biosimilars
1.2 Global Biosimilars Market: Flourishing

2. Engineering Behind Biosimilars
2.1 Designing From Scratch
2.2 Developing Biosimilars
2.2.1 Quality
2.2.2 Nonclinical Evaluation
2.2.3 Clinical Evaluation

3. Working of Biosimilars

4. Technical Innovations In Biosimilars
4.1 Improved Expression Systems
4.2 Higher Titers To Reduce Capacity Requirements
4.3 Analytical Technology
4.4 Quality By Design

5. Biosimilars & Generics : Different Or Same?

6. Budding US Biosimilar Market
6.1 Market Overview
6.2 US Biosimilar Pipeline Overview

7. FDA Rules & Regulations For Biosimilars Development & Market
7.1 Data Required For Approval
7.2 Need For Abbreviated Approval Pathway
7.3 Biosimilar User Fees
7.4 Biosimilars Action Plan

8. Biologics Coming Off Patent by 2025

9. FDA Approved Biosimilars

10. US – Approved & Marketed Biosimilars: Clinical, Price & Dosage
10.1 Retacrit (epoetin alfa-epbx)
10.2 Zarxio (filgrastim-sndz)
10.3 Nivestym (filgrastim-aafi)
10.4 Granix (tbo-filgrastim)
10.5 Inflectra (infliximab-dyyb)
10.6 Renflexis (infliximab-abda)
10.7 Fulphila (pegfilgrastim-jmdb)
10.8 Udenyca (pegfilgrastim-cbqv)

11. US – Approved Not Marketed Biosimilars
11.1 Trazimera (trastuzumab-qyyp)
11.2 Amjevita (adalimumab-atto)
11.3 Cyltezo (adalimumab-adbm)
11.4 Hyrimoz (adalimumab-adaz)
11.5 Mvasi (bevacizumab-awwb)
11.6 Erelzi (etanercept-szzs)
11.7 Ixifi (infliximab-qbtx)
11.8 Truxima (rituximab-abbs)
11.9 Ogivri (trastuzumab-dkst)
11.10 Herzuma (trastuzumab-pkrb)
11.12 Ontruzant (trastuzumab-dttb)

12. Tackling the High Price
12.1 Promote Competition
12.2 Shortening Exclusivity Period
12.3 Interchangeability
12.4 Extrapolation
12.5 Reforms for Cost Effective Drug

13. Payers: Concierge to US Biosimilar Market

14. US Biosimilar Market Dynamics
14.1 Market Drivers
14.2 Hurdles To Cross

15. US Biosimilar Market PEST Analysis

16. US Biosimilar Market Future Prospects

17. US – Biosimilars Clinical Pipeline by Company, Indication & Phase
17.1 Research
17.2 Preclinical
17.3 Clinical
17.4 Phase-I
17.5 Preregistration
17.6 Registered

18. US – Marketed Biosimilars Clinical Insight by Company & Indication
18.1 Adalimumab (Humira & Raheara)
18.2 Insulin Glargine Biosimilar (Abasaglar, Abasria & Basaglar)
18.3 Somatropin Biosimilar (Omnitrope & PrOmnitrope)
18.4 Insulin Lispro Biosimilar (Admelog & Insulin lispro Sanofi)
18.5 Trenonacog Alfa (IXINITY)
18.6 Pegfilgrastim Biosimilar – Biocon/Mylan
18.7 Infliximab Biosimilar (Flixabi & RENFLEXIS)
18.8 Bevacizumab Biosimilar (Mvasi)
18.9 Desvenlafaxine – Extended Release – Alembic

19. Suspended Biosimilars in Clinical Pipeline by Company, Indication & Phase
19.1 No Development Reported
19.2 Discontinued
19.3 Suspended

20. Competitve Landscape
20.1 Alembic
20.2 Allergan
20.3 Aptevo Therapeutics
20.4 Biocon
20.5 Celltrion
20.6 Eli Lilly
20.7 MedImmune
20.8 Pfizer
20.9 Polpharma
20.10 Samsung Bioepis
20.11 Sandoz
20.12 Sanofi
20.13 Teva

Figure 1-1: Geographic Division Of Biosimilar Market
Figure 1-2: Global - Biosimilars Market Share (%), 2018
Figure 2-1: Sources Of Variation Between Biosimilar Productions
Figure 2-2: Phases Of Biosimilar Development
Figure 2-3: Stages Of Comparability Exercise
Figure 2-4: New Drug Development: Cost & Time Comparison
Figure 3-1: Working Of Biosimilar On Active Rheumatoid Arthritis
Figure 4-1: Technology Needed For Cost Effectiveness Of Biosimilars
Figure 6-1: US - Filgrastim Market Share (%), 2018
Figure 6-2: US - Infliximab Market Share (%), 2018
Figure 6-3: US – Biosimilar Clinical Pipeline By Phase (%), 2019 till 2025
Figure 6-4: US – Biosimilar Clinical Pipeline By Phase (Number), 2019 till 2025
Figure 6-5: US – Biosimilar Discontinued in Clinical Pipeline By Phase (%),2019 till 2025
Figure 6-6: US – Biosimilar Discontinued in Clinical Pipeline By Phase (Number), 2019 till 2025
Figure 10-1: FDA Approved Biosimilars: Marketed
Figure 10-2: US - Cost Of 10 ml Retacrit In Different Concentration (US$), March'2019
Figure 10-3: US - Price Comparison In Different Concentration Of Zarxio & Neupogen (US$)
Figure 10-4: US - Cost Of Zarxio In Concentration – 300mgc/0.5 ml & 480mgc/0.8 ml (US$)
Figure 10-5: Wholesale Acquisition Cost Of Zarxio, Neupogen & Nivestym - 480mcg/ 0.8 ml (US$)
Figure 10-6: US - Cost Of Nivestym In Different Concentration (300mcg/0.5ml, 480mgc/0.8ml) (US$)
Figure 10-7: US - Cost Of 300 mcg Syringe & Vial Of Granix (US$)
Figure 10-8: US - Cost Of 480 mcg Syringe & Vial Of Granix (US$)
Figure 10-9: US - Cost Of Inflectra & Remicade For Injection dyyb 100 mg Powder (US$)
Figure 10-10: Global - Sale Of Inflectra & Remicade In 2017 (US$ Billions)
Figure 10-11: US - Sale Of Inflectra & Remicade In 2018 (US$ Billions)
Figure 10-12: US - Cost Difference Between Renflexis & Remicade (US$)
Figure 10-13: US - Cost Difference Between Renflexis & Inflectra (US$)
Figure 10-14: US - US - WAC Of Udenyca & Neulasta (US$)
Figure 10-15: US - WAC Of Udenyca & Neulasta (US$)
Figure 10-16: US - Cost Difference Between Udenyca, Fulphila, Neulasta For 6mg/0.6mL (US$)
Figure 11-1: US – Market Share Of Amjevita & Humira By 2032 (%)
Figure 11-2: US - WAC of Mvasi & Avastin (US$)
Figure 13-1: US - Prescription Drug Expenditure By Out of Pocket & Health Insurance (US$ Million), 2018 - 2025
Figure 13-2: US - Prescription Drug Expenditure By Out of Pocket & Health Insurance (US$ Million), 2018
Figure 13-3: US - Prescription Drug Expenditure By Out of Pocket & Health Insurance (%), 2018
Figure 13-4: US - Prescription Drug Expenditure By Out of Pocket & Health Insurance (US$ Million), 2025
Figure 13-5: US - Prescription Drug Expenditure By Out of Pocket & Health Insurance (%), 2025
Figure 13-6: Payers Strategies On Handling Biosimilars.
Figure 13-7: US - Health Care Expenditure By Out of Pocket & Health Insurance (US$ Million), 2018
Figure 13-8: US - Health Care Expenditure By Out of Pocket & Health Insurance (%), 2018
Figure 13-9: US - Health Care Expenditure By Out of Pocket & Health Insurance (US$ Million), 2025
Figure 13-10: US - Health Care Expenditure By Out of Pocket & Health Insurance (US$ Million), 2025
Figure 14-1: Main Therapeutics Areas Of Biosimilar Development (%), 2016
Figure 14-2: US - Share of generic and innovator products in small molecule and large molecule market (%)
Figure 15-1:PEST Analysis Of The Biosimilar Market
Figure 16-1: US - Biosimilar Market Opportunity(US$ Billion), 2019 - 2025
Figure 16-2: Global - GDP Expenditure On Healthcare (%), 2017
Figure 16-3: US - Savings by Biosimilar Molecule Class


【掲載企業】

Alembic, Allergan, Aptevo Therapeutics, Biocon, Celltrion, Eli Lilly, MedImmune, Pfizer, Polpharma, Samsung Bioepis, Sandoz, Sanofi, Teva

【免責事項】
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