Nemaura Medical Reports Financial Results for Third Quarter of Fiscal Year 2021 and Provides Corporate Update
Nemaura Medical Inc. (NASDAQ: NMRD) reported its fiscal Q3 2021 results, ending December 31, 2020, with a net loss of $1.45 million, compared to $445,000 the previous year. The company raised $20 million in non-dilutive funding and has a cash balance of $33 million as of February 15, 2021. Key developments include launching the beatdiabetes.life program and positive feedback from sugarBEAT users. R&D expenses decreased to $487,000, aligning with the product nearing commercial launch. Nemaura's market strategy targets the growing diabetes sector, projected to reach $59 billion by 2025.
- Raised $20 million in non-dilutive funding.
- Cash balance of $33 million as of February 15, 2021.
- Positive feedback from early sugarBEAT users.
- Progress towards commercial manufacture scale-up processes.
- Net loss increased to $1.45 million from $445,000 year-over-year.
- Absence of a $614,362 income tax benefit from the previous year.
- General and administrative expenses rose to $581,520.
Loughborough, England, Feb. 16, 2021 (GLOBE NEWSWIRE) -- Nemaura Medical Inc. (NASDAQ: NMRD) (“Nemaura” or the “Company”), a medical technology company focused on developing and commercializing non-invasive wearable diagnostic devices and supporting personalized lifestyle coaching programs, today announces financial results for its fiscal third quarter ending December 31, 2020 and provides a corporate update.
Recent and Third Quarter Highlights include:
- The Company continues to build the management team and strengthen resources for commercial revenue generation.
- Launched http://www.beatdiabetes.life in the U.S. which offers a program designed to help prevent, manage, or reverse Type 2 diabetes that combines a world class-diabetes management program originally developed at the Joslin Institute with the company’s proBEAT glucose monitoring sensor to help educate, inform, and guide users towards better management of their blood glucose levels. The program is initially being marketed to corporate payers and healthcare insurers in the U.S.
- Raised
$20 million in non-dilutive funding and, with a quarterly burn rate of approximately$1.5m , maintains substantial runway and leverage to accelerate its commercial growth.
- Continues to receive very positive feedback from early sugarBEAT users in the UK.
- Made further progress on its commercial manufacture scale-up processes to support product sales in key global territories.
- Made substantial progress towards its repurposed application for continuous temperature monitoring, with the device now ready for testing and submission for regulatory approvals.
Third Quarter 2020 Financial Results
Net loss for the third quarter of fiscal year 2021 was
Research and development expenses were
General and administrative expenses were
Cash as of December 31, 2020 was
About Nemaura Medical Inc.
Nemaura Medical Inc. is a medical technology company developing and commercializing non-invasive wearable diagnostic devices. The company is currently commercializing sugarBEAT® and proBEAT™. sugarBEAT®, a CE mark approved Class IIb medical device, is a non-invasive and flexible continuous glucose monitor (CGM) providing actionable insights derived from real time glucose measurements and daily glucose trend data, which may help people with diabetes and pre-diabetes to better manage, reverse, and prevent the onset of diabetes. Nemaura has submitted a PMA (Premarket Approval Application) for sugarBEAT® to the U.S. FDA. proBEAT™ combines non-invasive glucose data processed using artificial intelligence and a digital healthcare subscription service and is expected to be launched in the U.S. as a general wellness product.
The Company sits at the intersection of the global Type 2 diabetes market that is expected to reach nearly
For more information, please visit www.NemauraMedical.com.
Cautionary Statement Regarding Forward-Looking Statements:
The statements in this press release that are not historical facts may constitute forward-looking statements that are based on current expectations and are subject to risks and uncertainties that could cause actual future results to differ materially from those expressed or implied by such statements. Those risks and uncertainties include, but are not limited to, the launch of proBEAT™ in the US, risks related to regulatory status and the failure of future development and preliminary marketing efforts, Nemaura’s ability to secure additional commercial partnering arrangements, risks and uncertainties relating to Nemaura and its partners’ ability to develop, market and sell proBEAT™, the availability of substantial additional equity or debt capital to support its research, development and product commercialization activities, and the success of its research, development, regulatory approval, marketing and distribution plans and strategies, including those plans and strategies related to both proBEAT™ digital health, and sugarBEAT®. There can be no assurance that the company will be able to reach a part of or any of the global market for CGM with its products/services. The FDA reserves the right to re-evaluate their decision that proBEAT™ qualifies as a general wellness product should it become aware of any issues such as skin irritation or other adverse events from the device, as well as any misuse impacting patient safety, and any other reason as the FDA may see fit at its discretion to determine the product does not fit the definition of a general wellness product. These and other risks and uncertainties are identified and described in more detail in Nemaura’s filings with the United States Securities and Exchange Commission, including, without limitation, its Annual Report on Form 10-K for the most recently completed fiscal year, its Quarterly Reports on Form 10-Q, and its Current Reports on Form 8-K. Nemaura undertakes no obligation to publicly update or revise any forward-looking statements.
Contact:
Jules Abraham
CORE IR
917-885-7378
julesa@coreir.com
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