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The Gynecology Drugs Global Market Report 2022-31 by The Business Research Company describes and explains the global gynecology drugs market and covers 2016 to 2021, termed the historic period, and 2022 to 2026, termed the forecast period, along with further forecasts for the period 2026-2031. The report evaluates the market across each region and for the major economies within each region.

The Gynecology Drugs Global Market Opportunities And Strategies Report covers gynecology drugs market drivers, gynecology drugs market trends, gynecology drugs market segments, gynecology drugs market growth rate, gynecology drugs market major players, gynecology drugs market size and a special focus on identifying the trends, opportunities, and strategies that can lead to success.

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The Gynecology Drugs Global Market Opportunities And Strategies Report is the most comprehensive report available on this market and will help gain a truly global perspective as it covers 60 geographies in detail. O&S reports are available off the shelf and can be delivered to clients on the day of purchase. The chapter on the impact of COVID-19 gives valuable insights on supply chain disruptions, logistical challenges, and other economic implications of the virus on the market. The chapter also covers markets which have been positively affected by the pandemic.

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https://www.thebusinessresearchcompany.com/report/gynecology-drugs-market

A key gynecology drugs market trend:
The launch of gynecology drug treatments by major companies is a positive trend in the market. Due to the highly competitive nature of the market and the presence of various players, companies are focusing on new advanced drugs to manufacture and develop new treatments. For instance, in September 2021, Myovant Sciences, a UK-based biopharmaceutical company has announced that the U.S. Food and Drug Administration (FDA) accepted for review a supplemental New Drug Application (sNDA) for MYFEMBREE (relugolix 40 mg, estradiol 1 mg, and norethindrone acetate 0.5 mg) for the management of moderate to severe pain associated with endometriosis, a disorder in which tissue that normally lines the uterus grows outside the uterus. The FDA set a target action date of May 6, 2022 for this sNDA under the Prescription Drug User Fee Act (PDUFA). Furthermore, in April 2020, the FDA approved GlaxoSmithKline plc’s supplemental New Drug Application (sNDA) for Zejula (niraparib), an oral, once-daily poly (ADP-ribose) polymerase (PARP) inhibitor, as a monotherapy maintenance treatment for women with platinum-responsive advanced ovarian cancer regardless of biomarker status.

The report covers the gynecology drugs market segments:
1) By Therapeutics: Hormonal Therapy, Non-Hormonal Therapy
2) By Indication: Gynecology Cancers, Menopausal Disorder, Polycystic Ovary Syndrome, Contraception, Others
3) By Distribution Channel: Hospital Pharmacies, Retail Pharmacies, Online Pharmacies

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