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Our Company


INNOVATING WOMEN’S REPRODUCTIVE HEALTH THERAPEUTICS



For too long, women have been overlooked and undervalued. So it’s no surprise
that women’s reproductive health has suffered a similar fate. The consequence
runs deep, causing pain that isn’t just physical, but emotional, mental, and
financial, too. After all, in many cases this sits right at the heart of one of
our most basic drives in life: to secure our future.

Answering this critical unmet need takes extraordinary minds. Welcome to ObsEva.
Born in Switzerland in 2012, we’re a clinical-stage biopharmaceutical company
with the skills, experience, and backing to usher in a new era in women’s
reproductive health.

Our purpose is simple, bring to market the products women need. We think of
ourselves as the people who nurture your health when nature loses its way.


ObsEva. Nature meets Nurture

Learn more










Our Products


OUR PIPELINE


EBOPIPRANT



(OBE022)
Oral, investigational and selective
prostaglandin F2 alpha
receptor antagonist




COMMERCIAL RIGHTS

 * Exclusive Worldwide rights licensed to Organon

Learn more


NOLASIBAN



(OBE001)
Oral oxytocin
receptor antagonist




COMMERCIAL RIGHTS

 * Exclusive Worldwide (ex China)
 * Rights licensed to YuYuan Bioscience for development and commercialization in
   China (PRC)

Learn more
Latest Press Release


OBSEVA ANNOUNCES PROGRESS ON RESTRUCTURING INITIATIVES

September 13, 2022



Ad hoc announcement pursuant to Art. 53 LR of the SIX Swiss Exchange GENEVA,
Switzerland – September 13, 2022 –…



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OBSEVA IN THE MEDIA

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OTHER OBSEVA PRESS RELEASES

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WORK WITH US



Are you ready to join an innovative biopharmaceutical company that’s advancing
women’s reproductive health and pregnancy therapeutics?
Check out our vacancies and/or register to our talent community by clicking on
the link below.

Vacancies/Talent Community



 
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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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