Press release
Uterine Fibroids Pipeline Assessment growing over the forecast years 2019-2025
Uterine Fibroids Pipeline Assessment
Analyst Speak:
“The Uterine Fibroids Pipeline Assessment growing over the forecast years 2019-2025 owing to grow in R&D activities by the market players”
The uterine fibroids pipeline assessment increasing over the forecast years due to surge in the prevalence of uterine fibroid cases in female coupled with increase in the R&D activities for the development of newer drugs by the various pharmaceutical and biopharmaceutical companies. Moreover, patent expiries of block buster drugs, and fund raising public and private sectors for the development R&D activities are propel the uterine fibroids pipeline assessment over the forecast years. However, stringent regulatory guidelines, high R&D cost for the development of newer therapeutics and adverse effects with the newer therapeutics, hinder the uterine fibroids pipeline assessment over the forecast timeframe
Uterine Fibroids Pipeline Assessment market segmented on the basis of clinical phase, route of administration, and region. Based on clinical phase, uterine fibroid drugs are segmented into Phase I, Phase II, Phase III, and Phase IV therapeutics. Based on the route of administration, the market is segmented into oral, vaginal, and others.
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Most of the companies are present in the Phase III clinical trials with positive efficacy and safety results in the treatment of uterine fibroid treatment. For instance, In October 2017, Takeda Pharmaceuticals partnered with Myovant and announced the positive Phase III clinical studies results in the development of Relugolix, a uterine fibroid treatment drug. Moreover, AbbVie, Inc. and Neurocrine Biosciences collaborated in the development of uterine fibroid treatment drug Elagolix and announced the second positive Phase III clinical trial studies in March 2018.
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Key player’s profiles in the report are Repros Therapeutics Inc. (U.S.), Bayer AG (Germany), Takeda Pharmaceutical Company Ltd (Japan), AbbVie Inc. (U.S.), KISSEI PHARMACEUTICAL CO.,Ltd. (Japan), BioSpecifics Technologies Corporation (U.S.), and DONGKOOK Pharmaceutical Co., Ltd (Japan)
Precision Business Insights (PBI) in its report titled “Uterine Fibroids Pipeline Assessment”: Clinical Trails Analysis, Collaborations, Key Targets, Geographic Focus, and Data Publications, Competitor Analysis 2018. The report also covers therapeutics under Development by Companies/Institutes/Universities, the molecules in Pre-Registration, Filing rejected/withdrawn, Phase I, Phase II, Phase III, IND/CTA Filed, Preclinical, and Discovery
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https://www.precisionbusinessinsights.com/market-reports/uterine-fibroids-pipeline-drugs-assessment/#ulp-14mlyhjMGhVjZqa3
Detailed Segmentation
By Clinical Trial Phase
o Pre-clinical phase
o Phase-I
o Phase II
o Phase-III
By Route of Administration
o Oral
o Vaginal
o Others
Geography
o North America
• U.S
• Canada
o Europe
• Germany
• France
• U.K
• Italy
• Spain
• Russia
• Poland
• Rest of Europe
o Asia-Pacific
• Japan
• China
• India
• Australia & New Zealand
• ASEAN (Includes Indonesia, Thailand, Vietnam, Philippines, Malaysia, and Others)
• South Korea
• Rest of Asia-Pacific
o Latin America
• Brazil
• Mexico
• Argentina
• Venezuela
• Rest of Latin America
o Middle East and Africa (MEA)
• Gulf Cooperation Council (GCC) Countries
• Israel
• South Africa
• Rest of MEA
Get access to full summary @
https://www.precisionbusinessinsights.com/market-reports/uterine-fibroids-pipeline-drugs-assessment/
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