Pharmabiz
 

Roche seeks US FDA approval for AMH assay to use as lab analyzer

Basel, SwitzerlandSaturday, December 19, 2015, 10:00 Hrs  [IST]

Roche, a leader in research-focused healthcare, has filed a direct de novo application to the US Food and Drug Administration (FDA) for a fully automated Anti-Mullerian (AMH) assay for use on the company's full portfolio of laboratory analyzers. The determination of AMH is useful for the assessment of ovarian reserve in women presenting to infertility clinics for evaluation in conjunction with other clinical and laboratory findings.

"Our Elecsys AMH test will help physicians incorporate AMH testing into routine clinical practice and get more reliable results even faster than conventional protocols and manual AMH assays," explained Dr. Alan Wright, chief medical officer, Roche Diagnostics Corporation. "With over 7.4 million women in the US who have ever used fertility services and 1 in 8 couples having trouble getting or sustaining pregnancy, the need for a standardized, reproducible and robust fertility measurement for women has never been greater."

Serum levels of AMH have been shown to be relatively stable during the menstrual cycle with substantial fluctuations being observed in younger women. AMH levels further demonstrate lower intra- and inter-cyclic than baseline FSH. Measurement of serum AMH is used for the clinical assessment of ovarian reserve, an important measure for women who are either planning for pregnancy or struggling with infertility. The Elecsys AMH blood test produces standardized results for assessing ovarian reserve as compared with the use of ultrasound for assessing AFC in which the result is often dependent on the operator or clinic.

The assay is designed for use on all Roche immunoassay systems for low-, mid- and high-volume testing environments, including the cobas e 411, cobas e 601, cobas e 602 and Modular Analytics E170 analyzers.

"Once approved, this test will assist clinicians in more predictive, personalized fertility care for their patients," said Dr. Wright. "Our aim is to give healthcare providers confidence in their patient results and to give women a rapid answer (18 minutes) to a very important, deeply personal question about their fertility."

Roche currently offers an extensive menu of fertility assays that process in less than 18 minutes, allowing clinicians to evaluate patients quickly during their office visit.

In women, AMH is exclusively produced by granulosa cells of ovarian follicles during the early stages of follicle development. After an initial increase until early adulthood, AMH concentrations slowly decrease with increasing age until becoming undetectable around five years before menopause. However, major individual variability exists in the pace of follicle pool depletion and the initial size of the follicle pool, reflected by a wide range of age at menopause. Individual AMH serum concentration accurately reflects the size of the pool of antral follicles, representing the quantity of the remaining primordial follicles.

 
[Close]