Myriad Genetics Announces Prequel Prenatal Screening Can Now Be Performed Eight Weeks Into Pregnancy
Myriad Genetics Announces Prequel Prenatal Screening Can Now Be Performed Eight Weeks Into Pregnancy
SALT LAKE CITY, Nov. 19, 2024 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, announced that the Prequel Prenatal Screen is now available at eight weeks into pregnancy. Enabled by its AMPLIFY technology, Prequel is the first and only prenatal cell-free DNA (cfDNA) screen available at eight-weeks gestational age.
鹽湖城,2024年11月19日(全球新聞網)——萬基遺傳公司(納斯達克:MYGN),一家在基因檢測和精準醫療領域的領先者,宣佈Prequel產前篩查現已在懷孕八週時可用。得益於其AMPLIFY技術,Prequel是首個也是唯一一個在懷孕八週時可用的無細胞DNA(cfDNA)產前篩查。
"Previously, I would schedule my patients to come in at eight weeks for their first prenatal appointment; then, I would ask them to come back two weeks later to do a Prequel screen. Now that Prequel can be performed at eight weeks, patients have the opportunity to complete all baseline lab work during that initial care visit," said Dallas Reed, MD, FACMG, FACOG, obstetrician-gynecologist and medical geneticist who serves as the Principal Medical Advisor of Women's Health for Myriad Genetics. "As a result of this earlier timeframe, providers and their patients can obtain valuable genetic information earlier in the pregnancy, enabling them to make informed decisions based on that information sooner."
「之前,我會安排我的病人在懷孕八週時來進行第一次產前預約;然後,我會要求他們在兩週後再回來進行Prequel篩查。現在Prequel可以在八週時進行,病人在初次就診時有機會完成所有的基線實驗室工作,」致力於萬基遺傳婦女健康的首席醫療顧問、產科醫生兼醫學遺傳學家達拉斯·裏德博士說道。「由於這個時間提前,醫生和他們的病人可以在懷孕早期獲得有價值的遺傳信息,從而能夠根據這些信息更早地做出明智的決策。」
Having genetic insights earlier in the pregnancy may help expectant parents determine if they want to pursue diagnostic testing, find certain types of care and specialists, plan for the best place to deliver, and schedule appointments with board-certified genetic counselors as needed.
在懷孕早期獲得遺傳信息可能有助於準父母判斷他們是否希望進行診斷測試,尋找特定類型的護理和專家,規劃最佳分娩地點,並根據需要與經過認證的遺傳顧問預約。
"We are very excited to offer Prequel earlier in the pregnancy," said Melissa Gonzales, President of Women's Health, Myriad Genetics. "Myriad is committed to delivering reliable and validated genetic screens through investments in innovation such as AMPLIFY technology. By boosting the fetal DNA signal, providers can have higher confidence in the results for all their patients, including those with high BMIs.1"
「我們非常高興能夠在懷孕早期提供Prequel,」萬基遺傳婦女健康部門總裁梅利莎·岡薩雷斯表示。「萬基致力於通過對創新的投資,如AMPLIFY技術,提供可靠和經過驗證的遺傳篩查。通過增強胎兒DNA信號,醫生可以對所有病人的結果有更高的信懇智能,包括那些BMI較高的病人。」
About Prequel
Myriad's Prequel Prenatal Screen with AMPLIFY technology has been shown to increase the level of fetal DNA 2.3-fold on average2, allowing the test to provide pregnant patients with genetic insights into fetal development and the health of the pregnancy as early as eight weeks. The prenatal cfDNA screen can assess if a pregnancy is at an increased risk for several chromosomal conditions like Down, Edwards, or Patau syndrome, sex chromosome abnormalities, expanded aneuploidies, and select microdeletions, including 22q11.2.
關於Prequel
萬基遺傳的Prequel產前篩查採用AMPLIFY科技,已顯示胎兒DNA水平平均提高2.3倍2,使得該測試能夠在懷孕早期提供孕婦對胎兒發育和妊娠健康的基因洞察,最早可在孕八週時進行。產前cfDNA篩查可以評估妊娠是否面臨多個染色體異常的增高風險,例如唐氏綜合症、愛德華綜合症、帕陶綜合症、性染色體異常、擴展非整倍體以及特定微缺失,包括22q11.2。
About Myriad Genetics
Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well-being for all. Myriad develops and offers genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where genetic insights can significantly improve patient care and lower healthcare costs. For more information, visit .
關於Myriad Genetics
萬基遺傳是一家領先的基因檢測和精準醫學公司,致力於推進所有人的健康和福祉。萬基遺傳開發並提供基因檢測,幫助評估發病風險或疾病進展,並指導治療決策,涉及醫療專業領域的基因洞察可以顯著改善患者護理,並降低醫療保健成本。欲了解更多信息,請訪問。
Safe Harbor Statement
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to the company's commitment to delivering reliable and validated genetic screens through investments in innovation, such as AMPLIFY technology, and how by boosting the fetal DNA signal, providers can have higher confidence in all of their patients results, including those with high BMIs. These "forward-looking statements" are management's expectations of future events as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company's filings with the U.S. Securities and Exchange Commission, including the company's Annual Report on Form 10-K filed on February 28, 2024, as well as any updates to those risk factors filed from time to time in the company's Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. Myriad is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events, or otherwise except as required by law.
免責聲明
本新聞稿包含1995年《私人證券訴訟改革法案》意義上的「前瞻性聲明」,包括與公司致力於通過對創新的投資(如AMPLIFY科技)提供可靠和經過驗證的基因篩查相關的聲明,以及通過增強胎兒DNA信號,提供者可以對所有患者的結果,包括那些高BMI患者,擁有更高的信心。這些「前瞻性聲明」是管理層截至本聲明日期對未來事件的預期,且這些聲明面臨已知和未知的風險和不確定性,可能導致實際結果、條件和事件與預期的有重大不符和不利。此類因素包括在公司向美國證券交易委員會提交的文件中描述的風險,包括公司於2024年2月28日提交的10-K年度報告,以及公司不時在10-Q季度報告或8-K當前報告中提交的任何風險因素更新。萬基遺傳沒有任何義務,且明確聲明不承擔任何義務,去更新或更改任何前瞻性聲明,無論是由於新信息、未來事件或其他原因,除非法律要求。
Investor Contact
Matt Scalo
(801) 584-3532
IR@myriad.com
投資者聯繫方式
Matt Scalo
(801) 584-3532
IR@myriad.com
Media Contact
Glenn Farrell
(385) 318-3718
PR@myriad.com
媒體聯繫人
Glenn Farrell
(385) 318-3718
PR@myriad.com
1 BMI – body mass index
2 Welker, N.C., Lee, A.K., Kjolby, R.A.S. et al. High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening. Genet Med (2020).
1 BMI – 身體質量指數
2 Welker, N.C., Lee, A.k., Kjolby, R.A.S. 等人。高通量胎兒比例擴增提高了無創產前篩查的分析性能。基因醫學(2020年)。
譯文內容由第三人軟體翻譯。