Event calendar

ObsEva To Present Data on Two Clinical Development Programs at ESHRE Virtual 37th Annual Meeting

Details of the presentations for the Yselty program are as follows:

  • Title: Long-Term Secondary Efficacy of Linzagolix for Heavy Menstrual Bleeding (HMB) Due to Uterine Fibroids (UF): 52-Week Results from Two Placebo-Controlled, Randomized, Phase 3 Trials

Format: Oral presentation followed by a Q&A session

Presenter: Hugh Taylor, M.D., Professor and Chair of the Department of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine

Session Date & Time: Tuesday, June 29, 2021, at 4:15 PM CEST

  • Title: Efficacy and Safety of Linzagolix for the Treatment of Severe Adenomyosis: Initial Results from a Pilot Study

Format: ePoster

Presenter: Olivier Donnez, M.D., Ph.D., Co-founder and Co-CEO of the Institut du sein et de Chirurgie Gynécologique d’Avignon

Session Date & Time: ePosters will be available on-demand through the ESHRE conference portal, on Saturday June 26 starting at 7:00 AM CEST

Details of the presentation for the nolasiban program are as follows:

  • Title: The Effect of Nolasiban on Uterine Contractility at The Time of Embryo Transfer in in vitro Fertilisation Patients

Format: ePoster

Presenter: Connie Rees, M.D., investigator and physician specializing in obstetrics and gynecology, Catharina Hospital

Session Date & Time: ePosters will be available on-demand through the ESHRE conference portal, on Saturday June 26 starting at 7:00 AM CEST

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Disclaimer

Note that the following information contains information on investigational medicinal products. These products have not yet been approved for marketing by the European Medicines Agency or the U.S. Food and Drug Administration and are still under development. Further additional investigations may be needed in order for the marketing authorization to be granted, which grant may depend on a variety of factors and is not guaranteed. Click on “return” if you do not wish to receive such information. By clicking on “continue” you acknowledge that you wish to receive scientific information on our investigational products.

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Disclaimer

Note that the following information contains information on investigational medicinal products. These products have not yet been approved for marketing by the European Medicines Agency or the U.S. Food and Drug Administration and are still under development. Further additional investigations may be needed in order for the marketing authorization to be granted, which grant may depend on a variety of factors and is not guaranteed. Click on “return” if you do not wish to receive such information. By clicking on “continue” you acknowledge that you wish to receive scientific information on our investigational products.

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