“Acute Lymphoblastic Leukemia Market: Global Industry Analysis, Share, Size, Growth, Opportunity and Forecast 2019 – 2025” presents an in-depth assessment of the global Acute Lymphoblastic Leukemia market dynamics, opportunities, future roadmap, competitive landscape and discusses major trends. The report offers the most up-to-date industry data on the actual market situation and future outlook for the global Acute Lymphoblastic Leukemia market. The report includes historical data from 2014 to 2018 and forecasts until 2025.
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Top Leading Companies of Global Acute Lymphoblastic Leukemia Market are Erytech Pharma, Spectrum Pharmaceuticals, Pfizer, Sigma-Tau, Shire, Genzyme Corporatio, GSK, Amgen, EUSA Pharma, ARIAD Pharmaceuticals, Talon Therapeutics, Enzon, Inc., Nova Laboratories, Bristol-Myers Squibb, Silvergate Pharmaceuticals and others.
Additionally, the report provides key trends in terms of collaboration, merger & acquisition, distribution, exclusive and licensing agreements are analyzed with details. The report also explores the detailed description of growth drivers and inhibitors of the global Acute Lymphoblastic Leukemia market.
Global Acute Lymphoblastic Leukemia Market Split by Product Type and Applications:
This report segments the global Acute Lymphoblastic Leukemia market on the basis of Types are:
Stem cell Transplantation
On the basis of Application, the Global Acute Lymphoblastic Leukemia market is segmented into:
The Report Answers the Following Questions about the Global Acute Lymphoblastic Leukemia Market:
- How has the global Acute Lymphoblastic Leukemia market performed so far and how will it perform in the coming years?
- What are the key markets in the global Acute Lymphoblastic Leukemia industry?
- What are the key drivers and inhibitors in the current market?
- How is the market predicted to develop in the future?
- Who are the key players in this market space?
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- Approved drugs in the ALL space focus on a wide variety of targets. The majority of these therapies are administered via the intravenous route, with a few select products being available in oral and intramuscular formulations.
- Industry-sponsored drugs in active clinical development for ALL are spread evenly across Phase I and Phase II, with only one drug in Phase III.
- Therapies in mid-to-late-stage development for ALL focus on a wide variety of targets. The majority of pipeline drugs in mid-tolate-stage development are administered via the intravenous route, with the remainder being tested in oral formulations.
- The overall likelihood of approval of a Phase I hematologic asset is 10.1%, and the average probability a drug advances from Phase III is 57.7%. Drugs, on average, take 8.8 years from Phase I to approval, compared to 9.3 years in the overall oncology space.
- There have been 40 licensing and asset acquisition deals involving ALL drugs during 2014–19. The $1,220m strategic collaboration agreement signed in 2018 between Fate Therapeutics and Ono Pharmaceutical for the joint development and commercialization of two off-the-shelf CAR-T cell product candidates was the largest deal.
- The distribution of clinical trials across Phase I–IV indicates that the vast majority of trials for ALL have been in the early and midphases of development, with 91% of trials in Phase I–II, and only 9% in Phase III–IV.
- The US has a substantial lead in the number of ALL clinical trials globally. France leads the major EU markets, while China has the top spot in Asia.
- Clinical trial activity in the ALL space is dominated by completed trials. Novartis has the highest number of completed clinical trials for ALL, with 41 trials.
- Novartis leads industry sponsors with the highest overall number of clinical trials for ALL.
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