Cue Health to Launch Direct-to-Consumer Virtual Health Platform with COVID-19 Self-Test Approved by Google, Mayo Clinic, NBA and MLB

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Starting November 15, consumers can get Cue’s fast and accurate COVID-19 tests, 24/7 virtual care, e-prescription services, and CDC-compliant test results for travel: n anywhere, anytime

SAN DIEGO, November 9, 2021 / PRNewswire / – Cue Health (“Cue”) (Nasdaq: HLTH), a healthcare technology company, today announced the launch of its direct-to-consumer (DTC) virtual health platform on November 15, making Cue’s first COVID-19 molecular test available to people through United States through Cue’s new e-commerce site and integrated store. Individual consumers will now be able to harness the power of Cue’s COVID-19 test, which is already approved and used by world-class organizations like Google, Mayo Clinic, the NBA and MLB, among others. Earlier this year, the COVID-19 Cue test for home and over-the-counter (OTC) use was the first molecular test to receive FDA clearance for home use without a prescription. Beyond COVID-19 testing needs, Cue’s new membership offering – Cue + ™ – will provide members with 24/7 on-demand access to board-certified physicians, e-prescribing services, CDC-compliant travel test results via in-app video surveillance, and same-day delivery of Cue products to several major markets.

“Cue Health to launch DTC virtual health platform with its COVID-19 self-test approved by Google, Mayo Clinic, NBA and MLB”

Cue simplifies the COVID-19 testing process by combining the speed of rapid antigen testing with the lab-grade precision of PCR testing. Cue’s portable COVID-19 test showed 97.8% concordance with central lab PCR tests, as verified in a independent study driven by Mayo Clinic1. FDA cleared to test both symptomatic and asymptomatic adults and children two years of age and older using a lower nasal swab, Cue’s COVID-19 test provides a comfortable and stress-free testing experience . Test results are transmitted to the user’s smart mobile device in just 20 minutes.

“We have generated a lot of interest from the general public wanting to buy our COVID-19 tests: from parents who need to keep their children healthy in school to international business travelers to families who want to get together safely during the holiday season. are excited to make Cue available to a wider audience next week to provide fast and accurate COVID-19 testing at home or on the go, ”said Clint sever, co-founder and product manager of Cue.

Cue + membership not only meets people’s home testing needs, but also allows them to share Cue test results and discuss other health issues with a doctor on demand in the new Cue app. Health. The Cue platform is integrated with last mile delivery services so members can get products home when they need it most. And as expected COVID-19 antivirals requiring urgent administration hit the market, Cue expects to be able to allow consumers to go from test result to seeing a doctor and taking antiviral treatment, as the case may be. appropriate, in the comfort and convenience of their own homes.

“We’re excited to be able to offer consumers our best COVID-19 tests as part of Cue’s Integrated Care Platform, which we believe can help individuals and families live their healthiest lives,” said Ayub Khattak, co-founder and CEO of Cue. “With membership in Cue + and our new Cue Health app, we aim to make the healthcare journey – from testing to diagnosis to treatment – more accessible, more convenient and faster.”

The Cue experience begins with the Marker reader ($ 249), a reusable, compact device that processes each test and connects wirelessly with a user’s mobile device to deliver results in 20 minutes via the Health Cue App (for iOS and Android). The Cue player is compatible with Cue COVID-19 Test Cartridge ($ 225/ 3 pack) and other tests under development. Cue’s COVID-19 Tests are single-use, stand-alone cartridges that make testing simple and convenient. These products will be bundled together for discounts and available for purchase under two new Cue + membership packages when shop.cuehealth.com starts on November 15.

Features of the Cue + subscription:

  • Cue + Essential ™ ($ 49.99/month): Convenient, easy-to-use, lab-grade home testing and Cue Virtual Care to meet your needs anytime, anywhere. Ten COVID-19 tests per year, 20% off additional COVID-19 tests, and free same-day delivery in select markets. Reduced price on the Cue Reader (sold separately).

  • Cue + Complete ™ ($ 89.99/month): all the benefits of Cue + Essential, plus supervised, CDC-compliant COVID-19 testing for travel, work, or school. Even more COVID-19 tests (20 per year) and frontline access to future Cue care offerings.

Cue’s virtual healing capabilities will include:

  • CDC-compliant test results via in-app video surveillance for travel, work, and school (for Cue + Complete members)

  • 24/7 access to chat with certified doctors

  • New electronic prescriptions and prescription renewals

  • Laboratory tests ordered by a doctor

Cue aims to provide individuals with the ability to proactively monitor and manage their health, with actionable information they can share with healthcare providers in real time. Future care offerings planned by Cue – all of which are designed to be compatible with the Cue Reader – include products and services in the categories of respiratory health (such as influenza, RSV and strep throat), sexual health (as with chlamydia and gonorrhea), heart and metabolic health (as with cholesterol and HbA1c), women’s and men’s health, and chronic disease management.

For more information on Cue products and services available at November 15, please visit cuehealth.com.

Please download press material to accompany today’s announcement here.

About Cue Health
Cue Health (Nasdaq: HLTH) is a healthcare technology company that puts consumers in control of their health information and puts diagnostic information at the center of care. Cue Health empowers people to manage their health with real-time, actionable, and connected health information, giving individuals and their healthcare providers easy access to lab-quality diagnostics anywhere, no whenever, in a device that fits in the palm of your hand. The COVID-19 test, the first of its kind from Cue Health, was the first molecular diagnostic test cleared by the FDA for home and over-the-counter use without a prescription or physician supervision. Outside United States, Cue Health has received the CE Mark in the European Union, Interim Prescription Authorization from Health Canada and regulatory approval from india Central organization for the control of pharmaceutical standards. Cue was founded in 2010 and is headquartered in San Diego. For more information, please visit www.cuehealth.com.

Forward-looking statements
Statements in this press release regarding future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute “forward-looking statements”. The words, without limitation, “anticipate”, “believe”, “continue”, “could”, “estimate”, “‘wait”, “project”, “should”, “target”, “will”, “Would” and similar phrases are intended to identify forward-looking statements, although not all forward-looking statements contain these or similar identifying words. Actual results may differ materially from those indicated in these forward-looking statements due to various important factors, including the factors discussed in the “Risk Factors” section of the prospectus dated September 23, 2021 filed by Cue with the SEC. All forward-looking statements contained in this press release are based on the current expectations of Cue’s management team and speak only as of the date hereof, and Cue specifically disclaims any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise.

The COVID-19 Cue Test for Home and Over-the-Counter (OTC) Use and the COVID-19 Cue Test (for Professional Use) have not been authorized or approved by the FDA; but have been cleared by the FDA under an Emergency Use Clearance (EUA). These products have been authorized only for the detection of SARS-CoV-2 nucleic acid, not for other viruses or pathogens. Emergency use of these products is only authorized for the duration of the declaration of the existence of circumstances justifying the authorization of emergency use of in vitro diagnostics for the detection and / or diagnosis of COVID- 19 under Section 564 (b) (1) of the Federal Law. Food, Drug and Cosmetic Act, 21 USC § 360bbb-3 (b) (1), unless the statement is terminated or the authorization is earlier revoked.

1 In an independent study conducted by Mayo Clinic Laboratories, the overall agreement between Cue’s point-of-care test and reference laboratory tests was found to be 97.8%. Details of the study can be found here.

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SOURCE Cue Santé Inc.


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