bioLytical Laboratories Inc. Receives Health Canada Authorization for its INSTI® Multiplex HIV-1/2 Syphilis Antibody Test

bioLytical Laboratories Inc. announced today that it has launched its INSTI® Multiplex HIV-1/2 Syphilis Antibody Test for professional use in Canada

INSTI® Multiplex HIV-1/2 Syphilis Antibody Test

INSTI® Multiplex HIV-1/2 Syphilis Antibody Test Package

  • bioLytical has received Health Canada authorization to sell its INSTI® Multiplex HIV-1/2 Syphilis Antibody Test across Canada for professional use in point-of-care settings
  • By providing results for two infections with only one sample, the test helps reduce test anxiety for patients by allowing healthcare professionals to test more people in less time
  • The test is portable and can be performed in a multitude of settings with easy-to-understand results
  • As part of the Health Canada review and authorization, the submission included clinical data from the two-year PoSH Study led by researchers at the University of Alberta and St. Michael’s Hospital, a site of Unity Health Toronto
  • Test performance in clinical studies demonstrated high accuracy, with industry-leading sensitivity and specificity
  • bioLytical’s quality system is MDSAP: ISO 13485 certified

RICHMOND, British Columbia, March 27, 2023 (GLOBE NEWSWIRE) — bioLytical Laboratories Inc. (“bioLytical”), a global leader in rapid in-vitro medical diagnostics, announced today that it has received Health Canada authorization for its INSTI® Multiplex HIV-1/2 Syphilis Antibody Test, allowing its immediate entry into the Canadian market. Furthermore, bioLytical is working on a self-test version to ensure Canadians of all demographics can access regular and early testing for both infections, where and when it works best for them.

“I am proud to lead a team of hardworking and innovative individuals who consistently push the boundaries of what is possible,” says Rob Mackie, CEO of bioLytical. “Our continued dedication to excellence allowed us to achieve this remarkable milestone that will help Canadians across all demographics access early testing in various settings.”

As a well-known leader in global HIV testing with its innovative INSTI® HIV-1/2 Antibody Test, authorized by Health Canada for both professional and self-testing use, bioLytical has leveraged its proprietary INSTI® technology to develop the INSTI® Multiplex HIV-1/2 Syphilis Antibody Test, first approved and in use across Europe and Africa since 2016.

The test is designed to detect both HIV-1/2 and syphilis antibodies with one sample using a simple fingerprick method to deliver accurate results in one minute or less. Mobile and simple to use, INSTI® allows healthcare professionals to test in various environments, providing flexible options for persons that face barriers to accessing healthcare.

As part of Health Canada’s review and subsequent authorization, the two-year Point of Care Tests for Syphilis and HIV (PoSH) Study, completed between August 2020 and February 2022, was included in the submission process. The Study, led by researchers at the University of Alberta and St. Michael’s hospital, a site of Unity Health Toronto, showcased the importance of regular and frequent testing to help connect patients to care. Due to the real-time results that the innovative INSTI® platform provides, those who tested positive for HIV were either linked or relinked to care, and of those that tested positive for active syphilis, the majority (87.4%) were treated immediately following point-of-care test results, and the remaining participants were treated within a median of four days.

Syphilis is a serious health issue that can lead to long-term health consequences if left untreated. Canada is currently experiencing unprecedented syphilis infection rates, with a 166% nationwide increase from 2017-2021. Rates have increased across all demographics, with new infections increasing by 20% between 2020 and 2021 despite decreased access to STBBI services during the pandemic. Furthermore, there is a growing concern about increasing congenital syphilis, with a 1271% increase in the same period.

With an estimated 62,790 persons living with HIV (PLWH) in Canada and with an estimated 1,520 new HIV infections annually, co-infection with syphilis and HIV is a growing concern. While both infections can affect anyone, having a STI such as syphilis increases the chance of acquiring HIV and in PLWH, increases the chances of passing on HIV. Additionally, syphilis sores or ulcers can allow HIV and other STIs to enter the body.

Rapid testing is instrumental in ending HIV and syphilis as public health threats. Regular and early access to testing allows medical professionals to offer early interventions by quickly connecting patients to care and support, reducing onward transmission, and increasing awareness of prevention methods.

If syphilis is diagnosed within a year of infection, it can usually be treated with a single injection of medication. HIV treatment has also progressed significantly since the virus was identified over 40 years ago, allowing persons living with HIV to lead long and healthy lives on treatment. Creating a test that can identify both infections with a single sample helps ensure that Canadians can connect to care quickly and equitably. The INSTI® Multiplex HIV-1/2 Syphilis Antibody Test is an innovative and efficient approach to increasing access to early and regular testing for sexually transmitted and blood-borne infections (STBBIs) in Canada.

“With the rise of syphilis in Canada, including the concerning increase in congenital syphilis, there is an urgent need for a fast and reliable rapid diagnostic test,” said Mackie. “With the development of a highly accurate and innovative one-minute test, INSTI® allows Canadians to learn their status to two infections with only one drop of blood, helping more Canadians access testing, learn their status, and connect to care.”

bioLytical will manufacture the INSTI® Multiplex HIV-1/2 Syphilis Antibody Test in its MDSAP: ISO 13485-certified facility in British Columbia to sell and distribute across Canada. As a global leader in ultra-rapid infectious disease diagnostics, bioLytical is working to ensure our test kits are available to Canadians so they can know their status.

bioLytical Laboratories Inc. is a privately-owned Canadian company focused on researching, developing, and commercializing rapid in-vitro medical diagnostics using its proprietary INSTI® technology platform and its lateral flow line, iStatis. bioLytical has won several local and industry awards, including B.C. Exporter of the Year in 2019. We have been named Lifesciences B.C.’s Growth Stage Med Tech Company of the Year and featured on B.C.’s Fastest-Growing Companies for six years, including the Globe and Mail’s Fastest Growing Companies list in 2020. bioLytical moved to a significantly larger, state-of-the-art facility in Richmond, B.C., in 2020 to accommodate the extraordinary growth achieved through our team. Providing accurate results in one minute or less, the INSTI® range includes the INSTI® HIV-1/HIV-2 Antibody Test, INSTI® Multiplex HIV Syphilis Ab Test, INSTI® HIV Self Test, INSTI® Covid-19 Antibody Test, and the INSTI® HCV Antibody Test. bioLytical sells its products in Europe, North America, South America, Africa, and Asia. In 2022, bioLytical launched iStatis, its new lateral flow testing platform, to create additional access to testing worldwide.

By delivering accurate results in real-time, INSTI® and iStatis generate meaningful outcomes for medical professionals, patients, and public health organizations worldwide and is a key partner in tackling some of the world’s most severe healthcare challenges. Please visit www.istatis.com and www.insti.com, and www.biolytical.com for more information.

References

CATIE: https://www.catie.ca/syphilis-0
PHAC: https://www.canada.ca/en/public-health/services/reports-publications/canada-communicable-disease-report-ccdr/monthly-issue/2022-48/issue-11-12-november-december-2022/infectious-congenital-syphilis-canada-2021.html
PHAC: https://www.canada.ca/en/public-health/services/publications/diseases-conditions/estimates-hiv-incidence-prevalence-canada-meeting-90-90-90-targets-2020.html

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/4adaf035-89ca-428d-a01d-9bf5c3f05e4b

Media Contact
Stephanie Ritchie, Communications Specialist, bioLytical
[email protected]
+1-778-238-9340

GlobeNewswire Distribution ID 8795504

‫وزارة الصحة الكندية تمنح تصريحًا لشركة bioLytical Laboratories Inc. لاختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis

أعلنت شركة bioLytical Laboratories Inc. اليوم أنها أطلقت اختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis وأنه أصبح متاحًا للاستخدام من قبل المتخصصين في كندا.

  • حصلت bioLytical على تصريح من وزارة الصحة الكندية لطرح اختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis للبيع في جميع أنحاء كندا لاستخدامه من قبل المتخصصين في مرافق الرعاية الصحية
  • يقلل الاختبار من القلق لدى المرضى حيال إجراء الاختبارات حيث يتيح لأخصائيي الرعاية الصحية اختبار المزيد من الأشخاص في وقت أقل من خلال تقديم النتائج بخصوص اثنتين من العدوى باستخدام عينة واحدة فقط
  • الاختبار سهل الحمل ويمكن إجراؤه في العديد من الأماكن مع نتائج سهلة الفهم
  • وفي إطار المراجعة التي أجرتها وزارة الصحة الكندية ومنحها التصريح، تضمَّنت الوثائق المقدمة بيانات سريرية مستقاة من دراسة (PoSH) التي استغرقت عامين وأُجريت بقيادة باحثين في جامعة ألبرتا ومستشفى سانت مايكل وهو أحد المواقع التابعة لـ Unity Health Toronto
  • أظهر اختبار الأداء في الدراسات السريرية دقة عالية، مع حساسية وتخصصية رائدتين في الصناعة
  • نظام الجودة في bioLytical هو (MDSAP): حاصل على شهادة الجودة أيزو ISO 13485

ريتشموند، كولومبيا البريطانية، 27 مارس/آذار 2023 (GLOBE NEWSWIRE) – أعلنت شركة bioLytical Laboratories Inc. (“bioLytical”)، الشركة العالمية الرائدة في مجال التشخيص الطبي السريع في المختبرات، اليوم حصولها على تصريح من وزارة الصحة الكندية بخصوص اختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis لديها، ما يسمح بدخولها الفوري إلى السوق الكندية. بالإضافة إلى ذلك، تعمل bioLytical على تقديم إصدار اختبار ذاتي لضمان إمكانية حصول الكنديين من جميع الفئات السكانية على الاختبارات المنتظمة والمبكرة لكلتا العدوى، في أي وقت وفي أي مكان يكون فيه أكثر ملاءمة لهم.

صرَّح Rob Mackie، الرئيس التنفيذي لشركة bioLytical، قائلًا “أنا فخور بقيادة فريق من الأشخاص المتفانين والمبدعين الذين يوسعون آفاق ما هو ممكن على الدوام”، وأردف قائلًا “إن التزامنا المستمر بتحقيق التميز هو ما مكننا من الوصول إلى هذا الإنجاز الرائع الذي سيساعد الكنديين من جميع الفئات السكانية على إجراء الاختبارات المبكرة في مختلف الأماكن.”

ولكونها شركة رائدة معروفة في ميدان اختبارات فيروس نقص المناعة البشرية على مستوى العالم بفضل اختبار الأجسام المضادة المبتكر INSTI® HIV-1/2 المصرح به من قبل وزارة الصحة الكندية للاستخدام من قبل المتخصصين ولأغراض الاختبار الذاتي، استفادت شركة bioLytical من تقنية INSTI® لابتكار اختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis الذي تمت الموافقة عليه لأول مرة ويجري استخدامه في أوروبا وأفريقيا منذ عام 2016.

الهدف من الاختبار هو اكتشاف كل من الأجسام المضادة لفيروس نقص المناعة البشرية-1/2 والزهري من خلال عينة واحدة باستخدام طريقة وخز الإصبع البسيطة للحصول على نتائج موثوقة في دقيقة واحدة أو أقل. تتيح INSTI® لأخصائي الرعاية الصحية إجراء الاختبار في مختلف البيئات بفضل قابلية نقله وسهولة استخدامه، الأمر الذي يوفر خيارات مرنة للأشخاص الذين يواجهون صعوبة في الحصول على خدمات الرعاية الصحية.

وفي إطار المراجعة التي أجرتها وزارة الصحة الكندية ومنحها التصريح فيما بعد، تضمنت الوثائق المقدمة دراسة اختبار نقطة الرعاية لمرض الزهري وفيروس نقص المناعة البشرية (PoSH) التي أجريت في الفترة ما بين أغسطس 2020 وفبراير 2022. أظهرت الدراسة – التي أُجريت بقيادة باحثين في جامعة ألبرتا ومستشفى سانت مايكل وهو أحد المواقع التابعة لـUnity Health Toronto، أهمية الاختبارات المنتظمة والمتكررة كوسيلة لتسهيل وصول المرضى إلى خدمات الرعاية. وبفضل النتائج الفورية التي توفرها منصة INSTI® المبتكرة، فقد تم توصيل الأشخاص الذين ثبتت إصابتهم بفيروس نقص المناعة البشرية بخدمات الرعاية أو إعادة إيصالهم بها؛ وأما الأشخاص الذين ثبتت إصابتهم بمرض الزهري النشط، فقد تلقى غالبيتهم (87.4٪) العلاج على الفور بعد نتائج اختبار نقطة الرعاية، وتلقى باقي المشاركين العلاج غضون أربعة أيام في المتوسط.

يُعد مرض الزهري من المشكلات الصحية الخطيرة التي يمكن أن تؤدي إلى آثار طويلة المدى على الصحة إذا تُركت دون علاج. تشهد كندا حاليًا معدلات غير مسبوقة للإصابة بمرض الزهري، حيث ارتفعت بنسبة 166٪ من عام 2017 إلى عام 2021 على الصعيد الوطني. وارتفعت معدلات الإصابة في جميع الفئات السكانية، مع زيادة الإصابات الجديدة بنسبة 20٪ بين عامي 2020 و2021 في ظل انخفاض الوصول إلى خدمات العدوى المنقولة جنسياً والعدوى المنقولة عن طريق الدم أثناء جائحة كورونا. علاوة على ذلك، زادت حالات الإصابة بمرض الزهري الخلقي بنسبة 1271٪ خلال نفس الفترة، مما يسبب أيضًا قلقًا متزايدًا.

تشكِّل الإصابة بمرض الزهري وفيروس نقص المناعة البشرية في آن واحد مصدر قلق متزايد بالنظر إلى أن هناك ما يقدر بـ 62,790 شخصًا مصابًا بفيروس نقص المناعة البشرية في كندا وأن هناك ما يقرب من 1,520 حالة إصابة جديدة بفيروس نقص المناعة البشرية كل عام. وفي حين أن كلتا العدوتين يمكن أن تصيبا أي شخص، فإن الإصابة بعدوى منقولة جنسيًا مثل مرض الزهري تزيد من خطر الإصابة بفيروس نقص المناعة البشرية، فضلًا عن أنها تزيد من خطر انتقال فيروس نقص المناعة البشرية لدى المصابين بهذا الفيروس. من جانب آخر، يمكن لفيروس نقص المناعة البشرية وغيره من العدوى المنقولة جنسيًا أن يتسلل إلى الجسم من خلال القروح التي يسببها مرض الزهري.

ويعتبر الاختبار السريع ضروريًا للقضاء على مرض الزهري وفيروس نقص المناعة البشرية باعتبارهما من المخاطر التي تهدد على الصحة العامة. يتيح إجراء الاختبار بصورة منتظمة ومبكرة للمتخصصين في المجال الطبي تقديم التدخلات المبكرة عن طريق إيصال المرضى بخدمات الرعاية والدعم على وجه السرعة، والحد من انتقال العدوى، وزيادة الوعي بطرق الوقاية.

هذا ويمكن علاج مرض الزهري عادةً بحقنة بسيطة من الدواء إذا تم تشخيصه في غضون عام من الإصابة. وعلى الجانب الآخر، شهد علاج فيروس نقص المناعة البشرية تقدمًا ملحوظًا منذ اكتشاف الفيروس قبل أكثر من 40 عامًا، ما مكّن الأشخاص المصابين بفيروس نقص المناعة البشرية من العيش حياة طويلة وصحية أثناء تلقي العلاج. إن ابتكار اختبار يمكنه اكتشاف كلتا العدوتين من عينة واحدة يساعد على ضمان وصول الكنديين إلى الرعاية بشكل سريع ومنصف. يعتبر اختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis طريقة مبتكرة وفعالة لتوسيع نطاق الوصول إلى الاختبارات المبكرة والمنتظمة للعدوى المنقولة جنسياً والعدوى المنقولة عن طريق الدم في كندا.

صرح Mackie قائلًا “هناك حاجة ملحة لإجراء اختبار تشخيصي سريع وموثوق في ضوء ظهور مرض الزهري في كندا، فضلًا عن الزيادة المقلقة في الإصابة بمرض الزهري الخلقي”. وأضاف قائلًا “من خلال ابتكار اختبار دقيق للغاية ومبتكر مدته دقيقة واحدة، تتيح INSTI® للكنديين معرفة حالة إصابتهم باثنتين من العدوى بقطرة دم واحدة، وهو ما ساعد المزيد من الكنديين على إجراء الاختبار، ومعرفة حالة إصابتهم، والحصول على الرعاية.”

ستنتج شركة bioLytical اختبار الأجسام المضادة INSTI® Multiplex HIV-1/2 Syphilis في برنامج التدقيق الفردي للأجهزة الطبية (MDSAP) الخاص بها: وهي منشأة حاصلة على شهادة الجودة أيزو ISO 13485 في كولومبيا البريطانية للبيع والتوزيع في جميع أنحاء كندا. بصفتها شركة عالمية رائدة في تشخيص الأمراض المعدية فائقة السرعة، تعمل bioLytical على ضمان توفر مجموعات الاختبار لدينا للكنديين ليتمكنوا من معرفة حالة إصابتهم.

هذا وتعتبر شركة bioLytical Laboratories Inc.‎ شركة قطاع خاص كندية تعمل في مجالات البحث والتطوير والتسويق التجاري للتشخيصات الطبية السريعة في المختبرات، باستخدام منصتها التكنولوجية INSTI®‎ وخط الفحوص السريعة iStatis. وفازت bioLytical بالعديد من الجوائز المحلية والصناعية، بما في ذلك مُصدِّر العام في 2019 في بريتش كولومبيا. لقد حزنا لقب الشركة التقنية الطبية النامية لهذا العام في مجال علوم الحياة في بريتش كولومبيا، كما وشكّلنا مادة إعلامية دسمة بصفتنا أسرع الشركات نموًا في بريتيش كولومبيا لست أعوام، ومن ذلك دخولنا في قائمة الشركات الأسرع نموًا في عام 2020 لصحيفة جلوب أنجد ميل. وقد انتقلت bioLytical إلى مقر أحدث وأكبر بكثير، في ريتشموند، كولومبيا البريطانية، في عام 2020 لاستيعاب النمو الكبير الذي حققه فريقنا. من خلال تقديم نتائج دقيقة في دقيقة واحدة أو أقل، تشتمل مجموعة INSTI® على اختبار الأجسام المضادة INSTI® HIV-1/HIV-2، واختبار INSTI® Multiplex HIV Syphilis، واختبار INSTI® HIV الذاتي، واختبار الأجسام المضادة لكوفيد-19 INSTI®‎، واختبار الأجسام المضادة INSTI® HCV. تطرح bioLytical منتجاتها للبيع في أوروبا وأمريكا الشمالية وأمريكا الجنوبية وأفريقيا وآسيا. وقد أطلقت bioLytical منصة iStatis في عام 2022، وهي منصتها الجديدة لاختبار الفحوص السريعة لتوفير إتاحة أكبر للاختبار في جميع أنحاء العالم.

ومن خلال تقديم نتائج دقيقة في الوقت الفعلي، تقدم INSTI® وiStatis نتائج مهمة للمختصين الطبيين والمرضى ومؤسسات الصحة العامة في جميع أنحاء العالم، كما وتعتبر شريكًا مهمًا في معالجة بعض أكثر تحديات الرعاية الصحية خطورة في العالم. تفضل بزيارة www.istatis.com و www.insti.com و www.biolytical.com للاطلاع على مزيد من المعلومات.

المراجع

CATIE: https://www.catie.ca/syphilis-0

PHAC: https://www.canada.ca/en/public-health/services/reports-publications/canada-communicable-disease-report-ccdr/monthly-issue/2022-48/issue-11-12-november-december-2022/infectious-congenital-syphilis-canada-2021.html PHAC: https://www.canada.ca/en/public-health/services/publications/diseases-conditions/estimates-hiv-incidence-prevalence-canada-meeting-90-90-90-targets-2020.html

تتوفر الصورة المرفقة بهذا الإعلان عبر الرابط https://prdesk.globenewswire.com/api/ResourceLibraryFile/DownloadFile?source=pnr&Id=4adaf035-89ca-428d-a01d-9bf5c3f05e4b

جهة الاتصال الإعلامي:

Stephanie Ritchie، أخصائية الاتصالات في شركة bioLytical

[email protected]

‎+1-778-238-9340

GlobeNewswire Distribution ID 3511006

LeddarTech Releases LeddarVision Premium Surround, Its Latest Low-Level Fusion and Perception Product, to Support Automotive Level 2/2+ ADAS Applications

LeddarTech’s award-winning LeddarVision solution

LeddarVision technology recognized at Tech.AD USA and CES 2023

QUEBEC CITY, March 27, 2023 (GLOBE NEWSWIRE) — LeddarTech®, a global leader in providing the most flexible, robust and accurate ADAS and AD software technology, announces its third product launch since December with the LeddarVision™ Surround (LVS-2+). This product is a comprehensive fusion and perception software stack to support premium surround-view L2/L2+ ADAS highway assistance and 5-star NCAP 2025/GSR 2022 safety applications.

LeddarVision Surround (LVS-2+) is the latest low-level sensor fusion and perception product built on LeddarTech’s award-winning LeddarVision software. The LVS-2+ expands the company’s current product offering of the LeddarVision Front-Entry LVF-E and Front-High LVF-H. These products target entry- to premium-level ADAS applications.

The LVS-2+ efficiently extends the LVF front-view product family from a one-camera plus two to five-radar (1V2R-1V5R) sensor configuration to a five-camera plus five-radar (5V5R) configuration. This enhanced configuration supports ADAS functions such as traffic jam and highway assist applications, enabling automated lane changes, overtaking and extended speed range adaptive cruise control.

High-Performance and Cost-Effective

  • LeddarVision’s low-level fusion (LLF) technology pushes the performance envelope, extending the effective range of the sensors.
  • Low-level fusion optimally combines camera and radar modalities, achieving a high-performance system with reduced requirements per modality at a lower total sensing cost.
  • Superior accuracy in object separation and longitudinal position measurement on highways enables higher-performing adaptive cruise control implementation.
  • L2/L2+ highway assist, including adaptive cruise control up to 160 km/h, lane centering control, active lane change assist, traffic jam assist and highway assist (including auto-lane change support).

Safety

  • LVS-2+ addresses 5-star NCAP 2025/GSR 2022 safety applications.
  • Includes a built-in redundancy feature to accommodate sensor failures, degradations and conflicts.
  • LVS-2+ supports global scene attributes detection for operational design domain (ODD) analysis, sensor coverage and health monitoring features.

Flexible and Scalable

  • A comprehensive surround-view fusion and perception software platform that supports entry-level to premium ADAS highway assist Level 2/2+ applications.

Samples available: Contact LeddarTech for “A” samples of the LVS-2+ and “A” samples of the LVF-E and LVF-H products. LVS-2+ “B” sample availability is planned for late Q3 2023.

“LeddarTech is committed to supporting automotive Tier 1-2 suppliers and OEMs with software solutions and products that support enhanced safety features and lower overall development costs,” stated the company’s CEO, Charles Boulanger. “In December, we released our LVF products for entry-level to premium ADAS safety and highway assistance L2/L2+ applications, and in keeping with our commitment to continual product development, our newest product LeddarVision Surround (LVS-2+) further increases our software offering to our customers, with products that solve more safety issues with a scalable low-level fusion and perception software stack that offers higher performance at a lower cost,” Mr. Boulanger concluded.

LeddarTech launches the LVS-2+ officially at Automotive Tech.AD Berlin on March 27, 2023.

About LeddarTech

LeddarTech, a global software company founded in 2007, develops and provides comprehensive perception software solutions that enable the deployment of ADAS and autonomous driving applications. LeddarTech’s automotive-grade software applies advanced AI and computer vision algorithms to generate highly accurate 3D models of the environment, allowing for better decision making and safer navigation. This high-performance, scalable, cost-effective technology is leveraged by OEMs and Tier 1-2 suppliers to efficiently implement automotive and off-road vehicle ADAS solutions.

LeddarTech is responsible for several remote-sensing innovations, with over 150 patents granted or applied for that enhance ADAS and AD capabilities. Better awareness around vehicle is critical in making global mobility safer, more efficient, sustainable and affordable: this is what drives LeddarTech to become the most widely adopted sensor fusion and perception software solution.

Additional information about LeddarTech is accessible at www.leddartech.com and on LinkedIn, Twitter, Facebook and YouTube.

Contact:
Daniel Aitken, Vice-President, Global Marketing, Communications and Investor Relations, LeddarTech Inc.
Tel.: + 1-418-653-9000 ext. 232 [email protected]

Investor relations contact and website: InvestorRelations@leddartech.com
https://investors.leddartech.com/

Leddar, LeddarTech, LeddarVision, LeddarSP, VAYADrive, VayaVision and related logos are trademarks or registered trademarks of LeddarTech Inc. and its subsidiaries. All other brands, product names and marks are or may be trademarks or registered trademarks used to identify products or services of their respective owners.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/b7f20647-203a-42b4-b015-cedc2086ded5

GlobeNewswire Distribution ID 8793884

A LeddarTech lança o LeddarVision Premium Surround, seu mais recente produto de fusão de baixo nível e percepção, para apoiar as aplicações ADAS de nível 2/2+ no setor automotivo

CIDADE DO QUEBEC, March 27, 2023 (GLOBE NEWSWIRE) — A LeddarTech®, líder mundial no fornecimento da mais flexível, robusta e precisa tecnologia de software ADAS e AD, anuncia seu terceiro lançamento de produtos desde dezembro com o LeddarVision™ Surround (LVS-2+). Esse produto é uma pilha de software abrangente de fusão e percepção para apoiar as aplicações de assistência rodoviária premium surround-view L2/L2+ ADAS e de segurança 5 estrelas NCAP 2025/GSR 2022.

O LeddarVision Surround (LVS-2+) é o mais recente produto de baixo nível de fusão de sensores e percepção desenvolvido sobre o premiado software LeddarVision da LeddarTech. O LVS-2+ amplia a oferta atual de produtos da empresa da LeddarVision Front-Entry LVF-E e Front-High LVF-H. Esses produtos visam a entrada em aplicações ADAS de nível premium.

O LVS-2+ amplia eficientemente a família de produtos LVF de uma configuração de sensores com uma câmera mais dois a cinco radares (1V2R-1V5R) para uma configuração de cinco câmeras mais cinco radares (5V5R). Essa configuração aprimorada compatível com as funções ADAS, tais como engarrafamentos de trânsito e aplicações de assistência rodoviária, permitindo mudanças automáticas de faixa, ultrapassagens e controle de velocidade de cruzeiro adaptativo à faixa ampliada.

Alto desempenho e econômico

  • A tecnologia de fusão de baixo nível da LeddarVision (LLF) impulsiona o desempenho envolvente, ampliando o alcance efetivo dos sensores.
  • A fusão de baixo nível combina perfeitamente as modalidades de câmera e radar, alcançando um sistema de alto desempenho com requisitos reduzidos por modalidade a um custo total de detecção mais baixo.
  • A precisão superior na separação de objetos e medição da posição longitudinal em rodovias permite uma implementação de controle de cruzeiro adaptativo de maior desempenho.
  • A assistência rodoviária L2/L2+, incluindo o controle adaptativo de cruzeiro até 160 km/h, controle de centralização de faixa, assistência ativa de mudança de faixa, assistência em engarrafamentos de trânsito e assistência rodoviária (incluindo suporte de mudança automática de pista).

Segurança

  • O LVS-2+ aborda as aplicações de segurança 5 estrelas NCAP 2025/GSR 2022.
  • Inclui uma funcionalidade de redundância incorporada para acomodar falhas nos sensores, degradações e conflitos.
  • O LVS-2+ é compatível com a detecção de atributos de panorama global para análise do domínio de design operacional (ODD), cobertura de sensores e funcionalidades de monitoramento de saúde.

Flexível e Escalável

  • Uma plataforma de software abrangente de fusão e percepção de visão circundante que é compatível com aplicações de nível 2/2+ de assistência rodoviária ADAS premium.

Amostras disponíveis: Contacte a LeddarTech para obter amostras “A” dos produtos LVS-2+ e amostras “A” dos produtos LVF-E e LVF-H. A disponibilidade de amostras “B” do LVS-2+ está planejada para o final do 3.º trimestre de 2023.

“A LeddarTech está comprometida em apoiar os fornecedores automotivos de nível 1-2 e OEMs com soluções e produtos de software que são compatíveis com recursos de segurança aprimorados e custos de desenvolvimento mais baixos”, declarou o CEO da empresa, Charles Boulanger. “Em dezembro, lançamos nossos produtos LVF para aplicações L2/L2+ de segurança e assistência rodoviária ADAS premium, e de acordo com nosso compromisso com o desenvolvimento contínuo de produtos, nosso mais novo produto LeddarVision Surround (LVS-2+) aumenta ainda mais nossa oferta de software para nossos clientes, com produtos que resolvem mais problemas de segurança com uma pilha de software escalável com fusão baixo nível e percepção que oferece maior desempenho a um custo menor”, concluiu o Sr. Boulanger.

A LeddarTech lança oficialmente o LVS-2+ na Automotive Tech.AD Berlim em 27 de março de 2023.

Sobre a LeddarTech

A LeddarTech, uma empresa global de software fundada em 2007, desenvolve e fornece soluções abrangentes de software de percepção que permitem a implantação de ADAS e aplicações de condução autônoma. O software de grau automotivo da LeddarTech aplica algoritmos avançados de IA e visão computadorizada para gerar modelos 3D altamente precisos do ambiente, permitindo uma melhor tomada de decisão e uma navegação mais segura. Essa tecnologia de alto desempenho, escalável e econômica é alavancada por OEMs e fornecedores de nível 1-2 para implementar eficientemente as soluções ADAS para veículos automotivos e off-road.

A LeddarTech é responsável por várias inovações de detecção remota, com mais de 150 patentes concedidas ou requeridas que melhoram as capacidades ADAS e AD. Uma melhor consciência em torno do veículo é fundamental para tornar a mobilidade global mais segura, mais eficiente, sustentável e acessível: isso é o que leva a LeddarTech a se tornar a solução de software de fusão de sensores e percepção mais amplamente adotada.

Informações adicionais sobre a LeddarTech estão acessíveis em www.leddartech.com e no LinkedIn, Twitter, Facebook e YouTube.

Contato:
Daniel Aitken, Vice-Presidente, Marketing Global, Comunicações e Relações com Investidores, LeddarTech Inc.
Tel.: + 1-418-653-9000 ext. 232 [email protected]

Contato de Relações com Investidores e site: InvestorRelations@leddartech.com
https://investors.leddartech.com/

Leddar, LeddarTech, LeddarVision, LeddarSP, VAYADrive, VayaVision e os logotipos relacionados são marcas comerciais ou marcas registradas da LeddarTech Inc. e de suas filiais. Todas as outras marcas e nomes de produtos são ou podem ser marcas comerciais ou registradas usadas para identificar produtos ou serviços de seus respectivos proprietários.

A foto que acompanha este anúncio está disponível em https://www.globenewswire.com/NewsRoom/AttachmentNg/b7f20647-203a-42b4-b015-cedc2086ded5

GlobeNewswire Distribution ID 8793886

LeddarTech lance LeddarVision « Surround », son dernier logiciel de fusion de bas niveau et de perception, dédié aux applications ADAS automobiles de niveau 2/2+

La solution LeddarVision de LeddarTech plusieurs fois primée

La technologie LeddarVision récompensée à Tech.AD USA et CES 2023

QUÉBEC, 27 mars 2023 (GLOBE NEWSWIRE) — LeddarTech®, chef de file de calibre mondial dans les technologies logicielles pour systèmes avancés d’aide à la conduite (systèmes ADAS) et de conduite autonome (systèmes AD), annonce le lancement de son troisième produit depuis décembre avec le LeddarVision™ Surround (LVS-2+). Ce produit est une solution logicielle complète de fusion des données de capteurs et de perception dédiée aux applications ADAS haut de gamme de niveau 2/2+ d’aide à la conduite sur autoroute et de sécurité 5 étoiles NCAP 2025 et GSR 2022.

LeddarVision Surround (LVS-2+) est le dernier-né des solutions de fusion bas niveau des données de capteurs et de perception développées autour du logiciel primé LeddarVision de LeddarTech. Le LVS-2+ élargit l’offre de produits actuelle de l’entreprise, s’ajoutant au LeddarVision LVF-E (d’entrée de gamme) et au LVF-H (de niveau premium), deux solutions à vue frontale qui visent les applications ADAS d’entrée de gamme à supérieures.

Le LVS-2+ étend efficacement la configuration de capteurs 1V2R-1V5R (c.-à-d., 1 caméra + 2 à 5 radars) de la famille de produits à vue frontale LVF à une configuration 5V5R (c.-à-d., 5 caméras + 5 radars). Cette configuration bonifiée prend en charge des fonctionnalités ADAS comme l’aide à la conduite en embouteillage et l’aide à la conduite sur autoroute en permettant le changement de voie automatisé, le dépassement ainsi que la régulation de vitesse adaptative sur une plus grande plage de vitesse.

Une solution à haute performance et économique

  • La technologie de fusion de bas niveau LeddarVision repousse les limites du progrès technologique en augmentant la portée effective des capteurs.
  • La technologie utilisée combine de manière optimale les modalités de la caméra et du radar en procurant une performance élevée tout en réduisant les exigences de chaque modalité et le coût total de la détection.
  • Une précision supérieure dans la séparation des objets et dans la mesure de la position longitudinale sur autoroute permet une mise en œuvre plus performante de la fonction de régulation de vitesse adaptative.
  • Assistance sur autoroute de niveau 2/2+, incluant les fonctions de régulation de vitesse adaptative jusqu’à 160 km/h, centrage sur la voie, assistance active au changement de voie, aide à la conduite en embouteillage et aide à la conduite sur autoroute, y compris l’assistance automatique au changement de voie.

Sécurité

  • Le LVS-2+ s’adresse aux applications répondant aux exigences de sécurité 5 étoiles NCAP 2025 et GSR 2022.
  • Comprend une fonction de redondance intégrée pour pallier les éventuelles défaillances ou dégradations des capteurs ou contradictions entre ces derniers.
  • Prend en charge la détection des attributs de la scène globale pour les fonctionnalités d’aide à l’analyse ODD, de vérification de l’état des capteurs et d’autodiagnostic.

Flexible et modulaire

  • Une plateforme logicielle de fusion de données et de perception complète à vue périphérique qui vise les applications ADAS de niveau 2/2+ d’entrée de gamme à supérieures d’aide à la conduite sur autoroute.

Échantillons disponibles : communiquez avec LeddarTech pour des échantillons « A » du LVS-2+ ou du LVF-E/LVF-H. La disponibilité de l’échantillon « B » du LVS-2+ est prévue pour la fin du troisième trimestre 2023.

« LeddarTech s’engage à soutenir les fournisseurs automobiles de rang 1 et 2 et les équipementiers avec des solutions et des produits logiciels qui supportent des fonctions de sécurité bonifiées et permettent de réduire les coûts de développement globaux », a déclaré le chef de la direction de l’entreprise, Charles Boulanger. « En décembre, nous avons lancé nos produits LVF, à vue frontale, destinés aux applications ADAS de niveau 2/2+ d’aide à la conduite sur autoroute. Conformément à notre engagement à l’égard du développement soutenu de nouveaux produits, notre toute dernière solution, LeddarVision Surround (LVS-2+), augmente encore notre offre logicielle pour nos clients avec des produits qui résolvent davantage de problèmes de sécurité grâce à un logiciel évolutif de fusion de bas niveau et de perception offrant des performances supérieures à moindre coût », a conclu M. Boulanger.

LeddarTech procédera au lancement officiel du LVS-2+ lors de l’événement Automotive Tech.AD Berlin le 27 mars 2023.

À propos de LeddarTech

LeddarTech, une entreprise mondiale de logiciels fondée en 2007, développe et propose des solutions de perception logicielles complètes qui permettent le déploiement d’applications ADAS et de conduite autonome. Le logiciel de classe automobile de LeddarTech applique l’intelligence artificielle avancée et des algorithmes de vision numérique afin de générer des modèles 3D précis de l’environnement, pour une meilleure prise de décision et une navigation plus sûre. Cette technologie performante, évolutive et économique, permet la mise en œuvre efficace de solutions ADAS pour véhicules automobiles et hors route par les équipementiers et fournisseurs de rang 1 et 2.

Détentrice de plus de 150 brevets accordés ou déposés, l’entreprise a contribué à plusieurs innovations liées à des applications de télédétection et qui améliorent les capacités des systèmes d’aide à la conduite et de conduite autonome. Une plus grande prise de conscience est essentielle pour rendre la mobilité plus sûre, efficace, durable et abordable : c’est ce qui motive LeddarTech à devenir la solution logicielle de fusion des données de capteurs et de perception la plus largement adoptée.

Renseignements complémentaires disponibles sur www.leddartech.com et sur LinkedIn, Twitter, Facebook et YouTube.

Contact :
Daniel Aitken, vice-président, Marketing, communications et relations avec les investisseurs mondiaux, LeddarTech Inc.
Tél. : + 1-418-653-9000 poste 232 [email protected]

Contact relations investisseurs et site web : InvestorRelations@leddartech.com
https://investors.leddartech.com/

Leddar, LeddarTech, LeddarVision, LeddarSP, VAYADrive, VayaVision et les logos associés sont des marques de commerce ou des marques déposées de LeddarTech Inc. et de ses filiales. Tous les autres noms de marques, noms de produits et marques sont ou peuvent être des marques de commerce ou des marques déposées utilisées pour désigner les produits ou les services de leurs propriétaires respectifs.

Une photo accompagnant ce communiqué est disponible au :
https://www.globenewswire.com/NewsRoom/AttachmentNg/b7f20647-203a-42b4-b015-cedc2086ded5/fr

GlobeNewswire Distribution ID 8793884

ROSEN, NATIONAL TRIAL LAWYERS, Encourages SVB Financial Group Investors to Secure Counsel Before Important Deadline in Securities Class Action Filed by the Firm – SIVB

NEW YORK, March 26, 2023 (GLOBE NEWSWIRE) —

WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of the securities of SVB Financial Group (NASDAQ: SIVB) between June 16, 2021 and March 10, 2023, inclusive (the “Class Period”), of the important May 12, 2023 lead plaintiff deadline in the securities class action commenced by the Firm.

SO WHAT: If you purchased SVB securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.

WHAT TO DO NEXT: To join the SVB class action, go to https://rosenlegal.com/submit-form/?case_id=12882 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than May 12, 2023. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.

WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.

DETAILS OF THE CASE: According to the lawsuit, defendants throughout the Class Period made false and/or misleading statements and/or failed to disclose that: (1) the Company failed to disclose to investors the risks presented by impending rising interest rates; (2) the Company failed to disclose to investors that, in an environment with high interest rates, it would be worse off than banks that did not cater to tech startups and venture capital-backed companies; (3) the Company failed to disclose that, if its investments were negatively affected by rising interest rates, it was particularly susceptible to a bank run; (4) as a result, defendants’ public statements were materially false and/or misleading at all relevant times. When the true details entered the market, the lawsuit claims that investors suffered damages.

To join the SVB class action, go to https://rosenlegal.com/submit-form/?case_id=12882 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action.

No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor’s ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.

Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.

Attorney Advertising. Prior results do not guarantee a similar outcome.

——————————

Contact Information:

Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827
[email protected]
[email protected]
[email protected]
www.rosenlegal.com

GlobeNewswire Distribution ID 8795226

RVYL FINAL DEADLINE NOTICE: ROSEN, TRUSTED INVESTOR COUNSEL, Encourages RYVYL Inc. f/k/a Greenbox POS Investors to Secure Counsel Before Important April 3 Deadline in Securities Class Action Filed by the Firm – RVYL, GBOX

NEW YORK, March 26, 2023 (GLOBE NEWSWIRE) — WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of the securities of Ryvyl Inc. f/k/a Greenbox POS (NASDAQ: RVYL, GBOX): (i) pursuant and/or traceable to the registration statement and prospectus issued in connection with the Company’s January 29, 2021 public offering (the “Offering”); and/or (ii) between January 29, 2021 and January 20, 2023, both dates inclusive (the “Class Period”), of the April 3, 2023 lead plaintiff deadline in the securities class action commenced by the Firm.

SO WHAT: If you purchased Ryvyl securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.

WHAT TO DO NEXT: To join the Ryvyl class action, go to https://rosenlegal.com/submit-form/?case_id=11425 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than April 3, 2023. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.

WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.

DETAILS OF THE CASE: According to the lawsuit, the Registration Statement was false and/or misleading and/or failed to disclose that: (1) the Company would restate certain financials; (2) the Company’s internal controls were inadequate; (3) the Company downplayed and obfuscated its internal controls issues; and (4) as a result, the Registration Statement was materially false and/or misleading at all relevant times. When the true details entered the market, the lawsuit claims that investors suffered damages.

To join the Ryvyl class action, go to https://rosenlegal.com/submit-form/?case_id=11425 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action.

No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor’s ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.

Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.

Attorney Advertising. Prior results do not guarantee a similar outcome.

——————————

Contact Information:

Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827
[email protected]
[email protected]
[email protected]
www.rosenlegal.com

GlobeNewswire Distribution ID 8795216

ROSEN, GLOBAL INVESTOR COUNSEL, Encourages Rite Aid Corporation Investors With Losses to Secure Counsel Before Important Deadline in Securities Class Action Commenced by the Firm – RAD

NEW YORK, March 26, 2023 (GLOBE NEWSWIRE) — WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of the securities of Rite Aid Corporation (NYSE: RAD) between April 26, 2018 and March 13, 2023, both dates inclusive (the “Class Period”), of the important May 19, 2023 lead plaintiff deadline in the securities class action commenced by the firm.

SO WHAT: If you purchased Rite Aid securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.

WHAT TO DO NEXT: To join the Rite Aid class action, go to https://rosenlegal.com/submit-form/?case_id=9388 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than May 19, 2023. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.

WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.

DETAILS OF THE CASE: According to the lawsuit, defendants throughout the Class Period made false and/or misleading statements and/or failed to disclose that: (1) Until at least June 2019, Rite Aid filled at least hundreds of thousands of unlawful prescriptions for controlled substances that lacked a legitimate medical purpose, including for potentially lethal opioids such as oxycodone and fentanyl; (2) Rite Aid pharmacists filled these prescriptions despite clear “red flags” that indicated that the prescriptions were unlawful; (3) Rite Aid ignored evidence that its stores were dispensing unlawful prescriptions, and intentionally deleted internal notes about suspicious prescribers written by concerned pharmacists; (4) by knowingly filling unlawful prescriptions for controlled substances, Rite Aid violated the Controlled Substances Act and, where Rite Aid sought reimbursement from federal healthcare programs, also violated the False Claims Act; (5) as a result, it was at risk of prosecution by federal authorities such as the United States Department of Justice (“DOJ”) and (6) as a result, Defendants’ statements about its business, operations, and prospects, were materially false and misleading and/or lacked a reasonable basis at all times. When the true details entered the market, the lawsuit claims that investors suffered damages.

To join the Rite Aid class action, go to https://rosenlegal.com/submit-form/?case_id=9388 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action.

No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor’s ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.

Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.

Attorney Advertising. Prior results do not guarantee a similar outcome.

Contact Information:

Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827
[email protected]
[email protected]
[email protected]
www.rosenlegal.com

GlobeNewswire Distribution ID 8795342