New Merck Technology Aims to Further Optimize Embryo Incubation and Assessment
New Merck Technology Aims to Further Optimize Embryo Incubation and Assessment
PR67753
DARMSTADT, Germany, Mar. 12 /PRNewswire=KYODO JBN/ --
Merck integrates innovative Eeva(R) Test with Geri(TM) incubation platform,
bringing individualized incubation and outcome prediction together
Geri(TM)humidity technology aims to further advance incubation to precisely
monitor and manage the humidity level in the incubator Merck, a leading science
and technology company, today announced the release of two advanced Fertility
Technologies products for improved efficiency in the assisted reproductive
treatment (ART) lab, Eeva(R) Test 3.0 and Geri(TM) humidified incubation. These
first-in-class technologies will provide embryologists with in-depth
information and control over the environment in which the embryo grows to
support healthy embryo development and assessment.
"We believe Merck fertility technologies can accelerate clinics toward a new
standard for ART success," said Rehan Verjee, Chief Marketing and Strategy
Officer of biopharma business at Merck. "Since 2014 we've launched 28 products
in five product groups, providing new, state-of-the-art solutions that advance
fertility care."
The Eeva(R) Test 3.0 software supports embryo assessment within the ART lab,
using the established Xtend Algorithm. ART labs can now use this algorithm with
the Genea Biomedx-developed Geri(TM)+ incubator, integrating
bright-and-dark-field imaging together with Merck's proprietary software suite,
Geri(TM) Connect, Geri(TM) Assess. The combination of the Eeva(R) Test 3.0 with
the Geri(TM) incubator enables, for the first time, the application of the
clinically proven assessment algorithm of the Eeva(R) Test to support outcome
prediction with individualized incubation.
Geri(TM), ideated and created by Australian fertility technologies company
Genea Biomedx, has a broad range of additional modular features available that
can be selected by clinics to optimize culture conditions based on their needs.
Continually evolving, this unique offering now includes a specially designed
humidifier in addition to established features like Geri(TM) Connect, Geri(TM)
Assess or Geri(TM)+. The specially designed humidifier allows ART specialists
to precisely monitor and manage the humidity level in the incubator. Geri(TM)
is able to both monitor progress of embryo development through a real-time
camera and provide humidified incubation in individual chambers, thus providing
embryologists with more control to nurture embryo incubation and development.
Merck's ability to launch numerous technologies in the last two years is a
result of the company's strategy to combine market-leading drug treatments for
patients with breakthrough technologies tailored to the specific needs of the
ART lab. Combining the Eeva(R) Test and the Geri(TM) platform demonstrates
Merck's commitment to facilitating the connectivity between products, such as
the integration of these technologies, to leverage the data generated, thus
creating more informed decision making within the ART lab.
About Geri[TM]
Geri(TM) is a benchtop incubator with individually controlled incubation
chambers per patient to minimize disruptive events to the early-stage embryo.
It also incorporates a camera to real time monitor the developing embryos.
Integrating bright- and dark-field imaging, the Geri[TM]+ incubator allows for
combination with the Eeva(R) Test software. The Geri(TM) Connect software
allows the monitoring of embryos in real time through remote access to patient
and embryo data connected on the same network, while the Geri(TM) Assess
software is a user-defined scoring software used to assess and grade embryos on
their viability. As additional modular feature the portfolio includes a
specially designed humidifier, which allows ART specialists to precisely
monitor and manage the humidity level in the incubator.
Geri(TM) was developed by Genea Biomedx, a company that creates and
manufactures practical, accessible and precise fertility technologies that help
standardize and automate fertility treatment.
About the Eeva(R) Test
The non-invasive Early Embryo Viability Assessment (Eeva(R)) Test when used
adjunctively with traditional morphology may improve IVF outcomes by providing
IVF clinicians and patients with objective information on embryo viability. The
Eeva(R) Test utilizes proprietary software that automatically analyzes embryo
development against scientifically and clinically validated parameters. Its key
features include a multi-dimensional model for assessing and predicting the
development of embryos based on five key parameters including egg age, cell
stage durations of P2 and P3, post P3 analysis, and cell count. With the
Eeva(R) Test's quantitative data on each embryo's potential development, IVF
clinicians can improve the treatment path for their patients undergoing IVF
procedures.
Progyny Inc. granted Merck global marketing and commercialization rights for
the Progyny Eeva(R) Test software offering, aiming to provide customers
worldwide with innovative fertility technology solution. This new collaboration
builds on the successful relationship between both leaders in fertility
technologies, first established in 2010.
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About Merck
Merck is a leading science and technology company in healthcare, life
science and performance materials. Around 50,000 employees work to further
develop technologies that improve and enhance life - from biopharmaceutical
therapies to treat cancer or multiple sclerosis, cutting-edge systems for
scientific research and production, to liquid crystals for smartphones and LCD
televisions. In 2016, Merck generated sales of EUR 15.0 billion in 66 countries.
Founded in 1668, Merck is the world's oldest pharmaceutical and chemical
company. The founding family remains the majority owner of the publicly listed
corporate group. Merck, Darmstadt, Germany holds the global rights to the Merck
name and brand. The only exceptions are the United States and Canada, where the
company operates as EMD Serono, MilliporeSigma and EMD Performance Materials.
Contact: Dr. Raphaela Farrenkopf
+49-6151-72-2274
(Logo: http://mma.prnewswire.com/media/472778/Merck_Logo.jpg )
(Photo: http://mma.prnewswire.com/media/477184/Merck_Eeva_Test_3_0.jpg )
SOURCE: Merck
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