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ObsEva SA: ObsEva Announces Submission of New Drug Application to U.S. FDA for Linzagolix for the Treatment of Uterine Fibroids

ObsEva SA: ObsEva Announces Submission of New Drug Application to U.S. FDA for Linzagolix for the Treatment of Uterine Fibroids
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ObsEva : Announces Submission of New Drug Application to U.S. FDA for Linzagolix for the Treatment of Uterine Fibroids

ObsEva : Announces Submission of New Drug Application to U.S. FDA for Linzagolix for the Treatment of Uterine Fibroids
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ObsEva Announces Submission of New Drug Application to U.S. FDA for Linzagolix for the ...

ObsEva Announces Submission of New Drug Application to U.S. FDA for Linzagolix for the ...
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ObsEva Announces Two Cornerstone Publications Describing Clinical Trials of Nolasiban for ...

Press release content from Globe Newswire. The AP news staff was not involved in its creation.
ObsEva Announces Two Cornerstone Publications Describing Clinical Trials of Nolasiban for .
ObsEva SAAugust 4, 2021 GMT
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Geneva, Switzerland and Boston, MA – August 4, 2021 – ObsEva SA (NASDAQ: OBSV / SIX: OBSN), a biopharmaceutical company developing and commercializing novel therapies to improve women’s reproductive health, today announced the publication of two peer-reviewed papers on nolasiban, an oxytocin receptor antagonist in development for improving live birth rates in women undergoing embryo transfer following in-vitro fertilization (IVF).
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Human Reproduction. The study reports the results from a meta-analysis of three randomized, placebo-controlled trials showing that nolasiban increased the likelihood of live birth following IVF. Participants were administered a single oral dose of nolasiban 90 ....

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ObsEva SA: Organon and ObsEva Enter Global License Agreement to Develop and Commercialize Ebopiprant (OBE022), an Investigational Agent Being Evaluated as a First-in-Class Treatment for Preterm Labor

ObsEva SA: Organon and ObsEva Enter Global License Agreement to Develop and Commercialize Ebopiprant (OBE022), an Investigational Agent Being Evaluated as a First-in-Class Treatment for Preterm Labor
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