OSAKA, Japan, April, 16, 2021 - Shionogi & Co., Ltd. (Head Office: Osaka, Japan; President and CEO: Isao Teshirogi, Ph.D. ; hereafter “Shionogi”) is pleased to announce that it has concluded a joint sales contract with LumiraDx Japan Co., Ltd. (Head Office: Tokyo, Japan; President and CEO: Keisuke Kato) for its novel coronavirus (SARS-CoV-2) antigen test “LumiraDx SARS-CoV-2 Ag Test” and “LumiraDx Instrument” in Japan.
Early diagnosis is critical in preventing further spread of COVID-19, and various technological developments are currently in progress. The PCR(polymerase chain reaction) is currently the standard test method for diagnosing COVID-19, but there are still issues in terms of convenience and promptness of measurement. On the other hand, antigen tests have been put into practical use as a test method with excellent convenience and promptness. However, they have a lower sensitivity than the PCR, which is considered to be a challenge
The LumiraDx SARS-CoV-2 Ag Test was developed by LumiraDx (Head Office: London, UK; President and CEO: Ron Zwanziger) . The test combines high-sensitivity results comparable to those from the PCR with speed and efficiency (results in less than 12 minutes) using samples from a nasopharyngeal swab or nasal swab.1 The test and platform is already available in Japan, the United States, Europe, and other countries. Shionogi plans to launch sales in late May, 2021 in Japan. In the future, by developing new test items, it will be highly sensitive and convenient in the medical field as a platform that enables testing of a wide range of items such as clinical tests for other infectious diseases with one measuring device. LumiraDx’s platform will transform how patients will receive tests that used to be only available from a lab.
Shionogi is committed to “Protecting people worldwide from the threat of infectious diseases” as our key focus. We are not limiting ourselves to the research and development of therapeutic medications, but are also focused on the total care of infectious disease through awareness building, prevention and diagnosis and suppression of exacerbation. To contribute the restoration of social security and safety through the early end of the pandemic, Shionogi will provide this test agent and instrument to medical institute.
About LumiraDx Japan Co., Ltd.
LumiraDx Japan Co., Ltd. is the Japanese company of LumiraDx group, which is headquartered in the United Kingdom. Founded in 2014, LumiraDx develops, manufactures and commercializes an innovative point of care diagnostic platform designed to deliver lab comparable diagnostic results at the point of care in minutes. The company currently has a pipeline of 30 assays across common conditions including infectious disease, cardiovascular disease, diabetes, and coagulation disorders which will all help healthcare decisions affordable and accessible.
Please see the company website for details. LumiraDx Japan Co., Ltd. website
About LumiraDx SARS-CoV-2 Ag Test Strip
“LumiraDx SARS-CoV-2 Ag Test Strip” is a rapid microfluidic immunofluorescence assay that detects SARS-CoV-2 antigen in nasal swab specimens or nasopharyngeal swab specimens collected from individuals suspected of COVID-19 infection, with results in 12 minutes. In comparison with the PCR using samples from a nasopharyngeal swab, this antigen test agent has a positive agreement rate of 97.5% (39/40) and a negative agreement rate of 97.7% (210/215). In comparison with the PCR using samples from a nasal swab, the test has a positive agreement rate of 97.6% (81/83) and a negative agreement rate of 96.6% (168/174), showing high positive/negative agreement rates with the PCR1.
This announcement contains forward-looking statements. These statements are based on expectations in light of the information currently available, assumptions that are subject to risks and uncertainties which could cause actual results to differ materially from these statements. Risks and uncertainties include general domestic and international economic conditions such as general industry and market conditions, and changes of interest rate and currency exchange rate. These risks and uncertainties particularly apply with respect to product-related forward-looking statements. Product risks and uncertainties include, but are not limited to, completion and discontinuation of clinical trials; obtaining regulatory approvals; claims and concerns about product safety and efficacy; technological advances; adverse outcomes of important litigation; domestic and foreign healthcare reforms and changes of laws and regulations. Also for existing products, there are manufacturing and marketing risks, which include, but are not limited to, inability to build production capacity to meet demand, unavailability of raw materials and entry of competitive products. The company disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information, future events or otherwise.
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Shionogi & Co., Ltd.