Advancing Novel Therapeutics for Women’s Reproductive Health

ObsEva is advancing a pipeline of orally administered, clinical-stage innovative compounds to treat women’s reproductive health conditions.

Our Pipeline

Overview

ObsEva is advancing three product candidates through clinical development across a total of four indications.

Product candidate

Preclincal

Phase 1

Phase 2

Phase 3

Next milestones

Commercial rights

Linzagolix

(OBE2109)
Oral GnRH receptor antagonist

Positive 24W primary endpoint results
24 primary endpoint data Q2:20
MAA/NDA: Q4:20/Q1:21


Initiated Ph3 in Q2:19

Positive Phase 2b results in 2018/19




Exclusive worldwide (ex-Asia)

OBE022

Oral PGF2α receptor antagonist

Interim update in 60 patients Q1:20

Preclinical & phase 1 complete

Exclusive worldwide

Nolasiban

Oral oxytocin
receptor antagonist

Positive IMPLANT 2 ph3 results

IMPLANT 4 Ph3 missed primary endpoint


Exclusive worldwide (ex China)
Partnership with Yuyuan BioScience Technology (PRC)

* Study completed: Week 10 ongoing pregnancy primary endpoint met – Live Birth Rate secondary endpoint met

** Second Phase 3 trial (EU/Canada/Russia): recruitment completed (May2019)

*** Study completed: Primary and secondary endpoints met

Clinical Studies

We are currently conducting six international clinical research studies.

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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.

Continue