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Agreements

Date: 2014-04-03

Type of information: Licensing agreement

Compound: Early Embryo Viability Assessment (Eeva®) Test

Company: Merck Serono (Germany) Auxogyn (USA - CA)

Therapeutic area: Women health

Type agreement:

licensing
commercialisation

Action mechanism:

The Eeva Test is a non-invasive diagnostic test used adjunctively to traditional morphology. It utilizes time-lapse imaging and computer software to analyze embryo development, creating lab-based measurements that provide reproductive endocrinologists and embryologists with objective information which can help to assess embryo development and viability.

Disease:

Details:

* On April 3, 2014, Merck Serono has announced an exclusive license agreement with Auxogyn, a Californian company dedicated to advancing women’s reproductive health, for Auxogyn’s proprietary Early Embryo Viability Assessment (Eeva®) Test. The Eeva Test results deliver objective information that may assist clinicians in improving IVF (in vitro fertilization) patient outcomes. Under the terms of the agreement, Merck Serono will obtain exclusive rights to commercialize the Eeva Test® in Europe and Canada, with the option to extend to selected countries and regions. The license agreement builds on a successful relationship between the companies that was started in 2010 when Merck Serono initially invested in Auxogyn through a Series A Preferred Stock financing made by Merck Serono’s corporate venture capital fund, MS Ventures. In 2012, Merck Serono and Auxogyn announced a strategic partnership on the Eeva Test. Auxogyn received the CE mark for the Eeva System in 2012, and it is currently available for use in certain countries in the European Union and Canada. In the United States, where Auxogyn retains commercialization rights, Auxogyn has filed a submission with the FDA for the clearance of the Eeva System, and this application is currently under review by the FDA.

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