Nemaura Medical is developing non-invasive and minimally invasive wearable diagnostic devices,
coupled with artificial intelligence capabilities for digital healthcare. The company’s first product,
which is CE approved and undergoing commercial launch, is the sugarBEAT® non-invasive
continuous glucose monitoring device and BEAT®diabetes digital healthcare platform.
sugarBEAT® 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 help people with Type 1 or Type 2 diabetes and prediabetes respectively to better manage,
reverse and prevent the onset of diabetes. BEAT®diabetes is a health subscription service
providing 1-on-1 lifestyle coaching and behavior change recommendations driven by personalized
data provided by sugarBEAT®. Insulin users can also adjunctively use sugarBEAT® for insulin
dosage purposes when calibrated by a finger stick reading. sugarBEAT® is intended to be worn
during waking hours and consists of a daily disposable adhesive skin-patch connected to a
rechargeable transmitter, with an app displaying glucose readings at five-minute intervals.
Nemaura Medical (NASDAQ: NMRD) is a medical technology company developing sugarBEAT® as a non-invasive, affordable and flexible glucose trending device designed to provide persons with diabetes and pre-diabetics with an Ambulatory Glucose Profile (AGP) as a superior metric to better manage their blood sugar levels as compared to a HbA1c reading. SugarBEAT® consists of a daily disposable adhesive skin-patch connected to a rechargeable transmitter, with an app displaying glucose readings at five-minute intervals for periods up to 24 hours. SugarBEAT® can additionally be used as an adjunctive Continuous Glucose Monitoring (CGM) device by insulin users when calibrated by a finger stick reading.
Visit NMRDinfo.com for more information.
Nemaura Medical is developing non-invasive and minimally invasive wearable diagnostic devices,
coupled with artificial intelligence capabilities for digital healthcare. The company’s first product,
which is CE approved and undergoing commercial launch, is the sugarBEAT® non-invasive
continuous glucose monitoring device and BEAT®diabetes digital healthcare platform.
sugarBEAT® 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 help people with Type 1 or Type 2 diabetes and prediabetes respectively to better manage,
reverse and prevent the onset of diabetes. BEAT®diabetes is a health subscription service
providing 1-on-1 lifestyle coaching and behavior change recommendations driven by personalized
data provided by sugarBEAT®. Insulin users can also adjunctively use sugarBEAT® for insulin
dosage purposes when calibrated by a finger stick reading. sugarBEAT® is intended to be worn
during waking hours and consists of a daily disposable adhesive skin-patch connected to a
rechargeable transmitter, with an app displaying glucose readings at five-minute intervals.
Milestone Scientific Inc. (MLSS) is a biomedical technology research and development company that patents, designs, develops and commercializes innovative diagnostic and therapeutic injection technologies and instruments for medical and dental applications. Milestone's computer-controlled systems are designed to make injections precise, efficient, virtually painless, and less expensive. Milestone’s proprietary DPS® Dynamic Pressure Sensing technology® platform advances the development of next-generation devices, regulating flow rate and monitoring pressure from the tip of the needle, through platform extensions for local anesthesia for subcutaneous drug delivery, with specific applications for epidural space identification in regional anesthesia procedures.
Genetic Technologies Limited is a diversified molecular diagnostics
company developing tools for the prediction and assessment of cancer
risk to help physicians proactively manage patient health. The
Company’s lead products, ‘GeneType for Breast Cancer’ and
‘GeneType for Colorectal Cancer’, are clinically validated risk
assessment tests that are first in their class. The Company’s
development pipeline includes new tests for COVID-19, Type 2
diabetes, cardiovascular disease, prostate cancer, and melanoma.
Listed on the ASX in 2000 and NASDAQ in 2005, Genetic
Technologies has been a leader in the development and
commercialization of genetic risk assessment technology for 20 years.
Nemaura Medical Inc. (NASDAQ: NMRD), is a medical technology company developing sugarBEAT® as a non-invasive, affordable and flexible glucose trending device for use by persons with diabetes and pre-diabetics.
SugarBEAT® consists of a daily disposable adhesive skin-patch connected to a rechargeable transmitter, with an app displaying glucose readings at five minute intervals over periods up to 24 hours.
SugarBEAT® can additionally be used by insulin using persons with diabetes as an adjunctive glucose monitoring device when calibrated by a finger stick reading.
G Medical Innovations Holdings Ltd is a mobile health (mHealth) and e-health company. It develops and markets clinical and consumer medical-grade health monitoring solutions and offers end-to-end support for e-health projects. The company offers a suite of both consumer and clinical grade products and platforms which are positioned to reduce inefficiencies in healthcare delivery, improve access, reduce costs, increase the quality of care, and make healthcare more personalized and precise.
Tiziana Life Sciences is a dual-listed clinical stage biotechnology company focused on the discovery and development of novel molecules to treat human disease in oncology and immunology. Tiziana’s two lead drug candidates, Foralumab and Milciclib, uniquely target the root cause of diseases with large unmet needs in multibillion-dollar markets. Tiziana is accelerating development of anti-IL6 receptor monoclonal antibody (mAb) for treatment of COVID-19 lung inflammation. Foralumab is the only fully human anti-CD3 monoclonal antibody in clinical development in the world. This Phase 2 compound has potential application in a wide range of autoimmune and inflammatory diseases, such as nonalcoholic steatohepatitis (NASH), ulcerative colitis, multiple sclerosis, type-1 diabetes (T1D), Crohn's disease, psoriasis and rheumatoid arthritis, where modulation of a T-cell response is desirable. Tiziana is a market leader in the invention of proprietary technology for oral, nasal and inhaled formulation to transform immunotherapies with Monoclonal Antibodies currently administered intravenously. Also, Tiziana has a robust and growing patent portfolio.
Milestone Scientific Inc. (MLSS) is a biomedical technology research and development company that patents, designs, develops and commercializes innovative diagnostic and therapeutic injection technologies and instruments for medical and dental applications. Milestone's computer-controlled systems are designed to make injections precise, efficient, virtually painless, and less expensive. Milestone’s proprietary DPS® Dynamic Pressure Sensing technology® platform advances the development of next-generation devices, regulating flow rate and monitoring pressure from the tip of the needle, through platform extensions for local anesthesia for subcutaneous drug delivery, with specific applications for epidural space identification in regional anesthesia procedures.
Nemaura Medical (NASDAQ: NMRD) is a medical technology company developing sugarBEAT® as a non-invasive, affordable and flexible glucose trending device designed to provide persons with diabetes and pre-diabetics with an Ambulatory Glucose Profile (AGP) as a superior metric to better manage their blood sugar levels as compared to a HbA1c reading. SugarBEAT® consists of a daily disposable adhesive skin-patch connected to a rechargeable transmitter, with an app displaying glucose readings at five-minute intervals for periods up to 24 hours. SugarBEAT® can additionally be used as an adjunctive Continuous Glucose Monitoring (CGM) device by insulin users when calibrated by a finger stick reading.
Visit NMRDinfo.com for more information.
Nemaura Medical is developing non-invasive and minimally invasive wearable diagnostic devices,
coupled with artificial intelligence capabilities for digital healthcare. The company’s first product,
which is CE approved and undergoing commercial launch, is the sugarBEAT® non-invasive
continuous glucose monitoring device and BEAT®diabetes digital healthcare platform.
sugarBEAT® 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 help people with Type 1 or Type 2 diabetes and prediabetes respectively to better manage,
reverse and prevent the onset of diabetes. BEAT®diabetes is a health subscription service
providing 1-on-1 lifestyle coaching and behavior change recommendations driven by personalized
data provided by sugarBEAT®. Insulin users can also adjunctively use sugarBEAT® for insulin
dosage purposes when calibrated by a finger stick reading. sugarBEAT® is intended to be worn
during waking hours and consists of a daily disposable adhesive skin-patch connected to a
rechargeable transmitter, with an app displaying glucose readings at five-minute intervals.
Milestone Scientific Inc. (MLSS) is a biomedical technology research and development company that patents, designs, develops and commercializes innovative diagnostic and therapeutic injection technologies and instruments for medical and dental applications. Milestone's computer-controlled systems are designed to make injections precise, efficient, virtually painless, and less expensive. Milestone’s proprietary DPS® Dynamic Pressure Sensing technology® platform advances the development of next-generation devices, regulating flow rate and monitoring pressure from the tip of the needle, through platform extensions for local anesthesia for subcutaneous drug delivery, with specific applications for epidural space identification in regional anesthesia procedures.
Genetic Technologies Limited is a diversified molecular diagnostics
company developing tools for the prediction and assessment of cancer
risk to help physicians proactively manage patient health. The
Company’s lead products, ‘GeneType for Breast Cancer’ and
‘GeneType for Colorectal Cancer’, are clinically validated risk
assessment tests that are first in their class. The Company’s
development pipeline includes new tests for COVID-19, Type 2
diabetes, cardiovascular disease, prostate cancer, and melanoma.
Listed on the ASX in 2000 and NASDAQ in 2005, Genetic
Technologies has been a leader in the development and
commercialization of genetic risk assessment technology for 20 years.
Nemaura Medical Inc. (NASDAQ: NMRD), is a medical technology company developing sugarBEAT® as a non-invasive, affordable and flexible glucose trending device for use by persons with diabetes and pre-diabetics.
SugarBEAT® consists of a daily disposable adhesive skin-patch connected to a rechargeable transmitter, with an app displaying glucose readings at five minute intervals over periods up to 24 hours.
SugarBEAT® can additionally be used by insulin using persons with diabetes as an adjunctive glucose monitoring device when calibrated by a finger stick reading.
G Medical Innovations Holdings Ltd is a mobile health (mHealth) and e-health company. It develops and markets clinical and consumer medical-grade health monitoring solutions and offers end-to-end support for e-health projects. The company offers a suite of both consumer and clinical grade products and platforms which are positioned to reduce inefficiencies in healthcare delivery, improve access, reduce costs, increase the quality of care, and make healthcare more personalized and precise.
Tiziana Life Sciences is a dual-listed clinical stage biotechnology company focused on the discovery and development of novel molecules to treat human disease in oncology and immunology. Tiziana’s two lead drug candidates, Foralumab and Milciclib, uniquely target the root cause of diseases with large unmet needs in multibillion-dollar markets. Tiziana is accelerating development of anti-IL6 receptor monoclonal antibody (mAb) for treatment of COVID-19 lung inflammation. Foralumab is the only fully human anti-CD3 monoclonal antibody in clinical development in the world. This Phase 2 compound has potential application in a wide range of autoimmune and inflammatory diseases, such as nonalcoholic steatohepatitis (NASH), ulcerative colitis, multiple sclerosis, type-1 diabetes (T1D), Crohn's disease, psoriasis and rheumatoid arthritis, where modulation of a T-cell response is desirable. Tiziana is a market leader in the invention of proprietary technology for oral, nasal and inhaled formulation to transform immunotherapies with Monoclonal Antibodies currently administered intravenously. Also, Tiziana has a robust and growing patent portfolio.
Milestone Scientific Inc. (MLSS) is a biomedical technology research and development company that patents, designs, develops and commercializes innovative diagnostic and therapeutic injection technologies and instruments for medical and dental applications. Milestone's computer-controlled systems are designed to make injections precise, efficient, virtually painless, and less expensive. Milestone’s proprietary DPS® Dynamic Pressure Sensing technology® platform advances the development of next-generation devices, regulating flow rate and monitoring pressure from the tip of the needle, through platform extensions for local anesthesia for subcutaneous drug delivery, with specific applications for epidural space identification in regional anesthesia procedures.
Cidara is developing long-acting therapeutics designed to improve the standard of care for patients facing serious diseases. The Company’s portfolio is comprised of drug candidates intended to transform existing treatment and prevention paradigms. Its lead Phase 3 antifungal candidate, rezafungin, will report Phase 3 data at the end of 2021. The potential peak sales opportunity for rezafungin in the US is ~$750M. In addition, the Company is developing Drug-Fc Conjugates (DFCs) targeting viral and oncology diseases from Cidara’s proprietary Cloudbreak® platform.
Nutriband is a transdermal focused pharmaceutical company based in the United States with a goal to improve the safety, comfort and efficacy of existing drugs using transdermal technologies. The Company is developing a pharmaceutical pipeline to improve drug delivery technologies and capabilities for patients, physicians, and payers through transdermal delivery technologies. Nutriband’s lead product is its AVERSA® technology. AVERSA® abuse deterrent transdermal technology incorporates aversive agents to prevent the Abuse, DiVERsion, MiSuse and Accidental exposure of drugs with abuse potential, such as opioids. The Company’s first application for AVERSA® is an abuse deterrent fentanyl transdermal patch which it is developing to provide clinicians and patients a safe extended-release patch for chronic pain. The goal is to make opioid based pain treatments safe for all who need them. AVERSA technology has received patent protection in the European Union, Australia, Japan, Mexico, Russia with patent prosecution in the US and Canada. Nutriband has made sure to target all large applicable markets and its global patent protection has opened up many opportunities for the Company to make a big impact on the safety profile of drugs globally.
Nemaura Medical (NASDAQ: NMRD) is a medical technology company developing sugarBEAT® as a non-invasive, affordable and flexible glucose trending device designed to provide persons with diabetes and pre-diabetics with an Ambulatory Glucose Profile (AGP) as a superior metric to better manage their blood sugar levels as compared to a HbA1c reading. SugarBEAT® consists of a daily disposable adhesive skin-patch connected to a rechargeable transmitter, with an app displaying glucose readings at five-minute intervals for periods up to 24 hours. SugarBEAT® can additionally be used as an adjunctive Continuous Glucose Monitoring (CGM) device by insulin users when calibrated by a finger stick reading.
Medistein is a new startup for portable medical devices. Our vision is to improve the health outcomes of mobile and home-based patients. We propose to achieve this vision by building a world-‐class consumer medical devices company that develops portable, user-friendly and state of the art healthcare products.
Lantern Pharma is a clinical stage biotechnology company focused on leveraging artificial intelligence (“A.I.”), machine learning and genomic date to streamline the drug development process and to identify patients who will benefit from their targeted oncology therapies. Their portfolio of therapies consists of compounds that others have tried, but failed, to develop into an approved commercialized drug. Additionally, they develop new compounds with the assistance of their A.I. platform (RADR) and biomarker driven approach. The Company is currently developing four therapeutic programs.
In MakroCare whitepaper, we have compiled and simplified some of these new policies, revisions, regulatory amendments from registration, labeling, safety reporting, renewal, publishing /eCTD submission of last year and forthcoming years.
BioVie Inc. (NASDAQ: BIVI) is a clinical-stage company developing innovative drug therapies for liver disease. The Company’s drug candidate, BIV201 (continuous infusion terlipressin), has an Orphan Drug designation for the treatment of refractory ascites, FDA Fast Track status, and US patent pending. BIV201 also has an Orphan Drug designation for the treatment of hepatorenal syndrome (HRS). The active agent in BIV201, terlipressin, is approved for use in about 40 countries for the treatment of related complications of advanced liver cirrhosis but is not available in the US or Japan. The FDA has never approved terlipressin. BioVie is targeting this landmark achievement.
One in 8 U.S. women will develop invasive breast cancer over her lifetime, with approximately 266,000 new breast cancer patients and 3.1 million breast cancer survivors in 2018. Following breast cancer surgery in the adjuvant setting, a HER2/neu 3+ patient typically receives Herceptin® in the first year, with the hope that their breast cancer will not recur, and with the odds of recurrence slowly decreasing over the first 5 years after surgery. Herceptin® has been shown to reduce recurrence rates from 25% to 12% in the adjuvant setting. In the neoadjuvant setting, a patient receives treatment before surgery and based on the results of a biopsy at surgery, will receive the same or more potent treatment after surgery. Kadcyla® has been shown to reduce recurrence rates from 22% to 11% in the neoadjuvant setting. Accordingly, we believe that GP2 may be used to address the 50% of recurring patients who do not respond to either Herceptin® or Kadcyla®.
Safer Technologies Program for Medical DevicesEMMAIntl
FDA has introduced a new program for medical devices and for device led combination products. Under this program are devices that do not qualify to be cleared via the breakthrough program but significantly improve the safety of the currently available options that treat diseases that are non-life threatening...
Lantern Pharma is a clinical stage biotechnology company focused on leveraging artificial intelligence (“A.I.”), machine learning and genomic date to streamline the drug development process and to identify patients who will benefit from their targeted oncology therapies. Their portfolio of therapies consists of compounds that others have tried, but failed, to develop into an approved commercialized drug. Additionally, they develop new compounds with the assistance of their A.I. platform (RADR) and biomarker driven approach. The Company is currently developing four therapeutic programs.
SciSparc is a specialty pharmaceutical company developing unique cannabinoid technologies for treatment of central nervous system disorders. The proprietary compounds capitalize on the biochemistry of receptors that specialize in modulating the central nervous system (CNS) to create therapeutics that mitigate the adverse symptoms associated with CNS disorders.
Cidara is developing long-acting therapeutics designed to improve the standard of care for patients facing serious diseases. The Company’s portfolio is comprised of drug candidates intended to transform existing treatment and prevention paradigms. Its lead Phase 3 antifungal candidate, rezafungin, will report Phase 3 data at the end of 2021. The potential peak sales opportunity for rezafungin in the US is ~$750M. In addition, the Company is developing Drug-Fc Conjugates (DFCs) targeting viral and oncology diseases from Cidara’s proprietary Cloudbreak® platform.
Second Sight Medical Products, a recognized global leader in neuromodulation devices for blindness, announced a definitive agreement on February 7, 2022, under which privately held Nano Precision Medical (NPM) will merge with a wholly owned subsidiary of Second Sight in an all-stock transaction. NPM will be the surviving company and owned by Second Sight. The resulting company will focus on development of innovative drug and device medical implants that treat chronic diseases with high unmet medical need.
Exact Sciences chairman and CEO Kevin Conroy delivered the company's presentation at the 2015 Baird 2015 Healthcare Conference in New York at 9:40 a.m. ET on Wednesday, Sept. 9.
An archive of the webcast is available here: http://wsw.com/webcast/baird43/register.aspx?conf=baird43&page=exas&url=http://wsw.com/webcast/baird43/exas/index.aspx
Nemaura Medical 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 as a general wellness product as part of its BEAT®diabetes program that is currently undergoing pilot studies.
Nemaura Medical is developing non-invasive and minimally invasive wearable diagnostic devices,
coupled with artificial intelligence capabilities for digital healthcare. The company’s first product,
which is CE approved and undergoing commercial launch, is the sugarBEAT® non-invasive
continuous glucose monitoring device and BEAT®diabetes digital healthcare platform.
sugarBEAT® 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 help people with Type 1 or Type 2 diabetes and prediabetes respectively to better manage,
reverse and prevent the onset of diabetes. BEAT®diabetes is a health subscription service
providing 1-on-1 lifestyle coaching and behavior change recommendations driven by personalized
data provided by sugarBEAT®. Insulin users can also adjunctively use sugarBEAT® for insulin
dosage purposes when calibrated by a finger stick reading. sugarBEAT® is intended to be worn
during waking hours and consists of a daily disposable adhesive skin-patch connected to a
rechargeable transmitter, with an app displaying glucose readings at five-minute intervals.
Cidara is developing long-acting therapeutics designed to improve the standard of care for patients facing serious diseases. The Company’s portfolio is comprised of drug candidates intended to transform existing treatment and prevention paradigms. Its lead Phase 3 antifungal candidate, rezafungin, will report Phase 3 data at the end of 2021. The potential peak sales opportunity for rezafungin in the US is ~$750M. In addition, the Company is developing Drug-Fc Conjugates (DFCs) targeting viral and oncology diseases from Cidara’s proprietary Cloudbreak® platform.
Nutriband is a transdermal focused pharmaceutical company based in the United States with a goal to improve the safety, comfort and efficacy of existing drugs using transdermal technologies. The Company is developing a pharmaceutical pipeline to improve drug delivery technologies and capabilities for patients, physicians, and payers through transdermal delivery technologies. Nutriband’s lead product is its AVERSA® technology. AVERSA® abuse deterrent transdermal technology incorporates aversive agents to prevent the Abuse, DiVERsion, MiSuse and Accidental exposure of drugs with abuse potential, such as opioids. The Company’s first application for AVERSA® is an abuse deterrent fentanyl transdermal patch which it is developing to provide clinicians and patients a safe extended-release patch for chronic pain. The goal is to make opioid based pain treatments safe for all who need them. AVERSA technology has received patent protection in the European Union, Australia, Japan, Mexico, Russia with patent prosecution in the US and Canada. Nutriband has made sure to target all large applicable markets and its global patent protection has opened up many opportunities for the Company to make a big impact on the safety profile of drugs globally.
Nemaura Medical (NASDAQ: NMRD) is a medical technology company developing sugarBEAT® as a non-invasive, affordable and flexible glucose trending device designed to provide persons with diabetes and pre-diabetics with an Ambulatory Glucose Profile (AGP) as a superior metric to better manage their blood sugar levels as compared to a HbA1c reading. SugarBEAT® consists of a daily disposable adhesive skin-patch connected to a rechargeable transmitter, with an app displaying glucose readings at five-minute intervals for periods up to 24 hours. SugarBEAT® can additionally be used as an adjunctive Continuous Glucose Monitoring (CGM) device by insulin users when calibrated by a finger stick reading.
Medistein is a new startup for portable medical devices. Our vision is to improve the health outcomes of mobile and home-based patients. We propose to achieve this vision by building a world-‐class consumer medical devices company that develops portable, user-friendly and state of the art healthcare products.
Lantern Pharma is a clinical stage biotechnology company focused on leveraging artificial intelligence (“A.I.”), machine learning and genomic date to streamline the drug development process and to identify patients who will benefit from their targeted oncology therapies. Their portfolio of therapies consists of compounds that others have tried, but failed, to develop into an approved commercialized drug. Additionally, they develop new compounds with the assistance of their A.I. platform (RADR) and biomarker driven approach. The Company is currently developing four therapeutic programs.
In MakroCare whitepaper, we have compiled and simplified some of these new policies, revisions, regulatory amendments from registration, labeling, safety reporting, renewal, publishing /eCTD submission of last year and forthcoming years.
BioVie Inc. (NASDAQ: BIVI) is a clinical-stage company developing innovative drug therapies for liver disease. The Company’s drug candidate, BIV201 (continuous infusion terlipressin), has an Orphan Drug designation for the treatment of refractory ascites, FDA Fast Track status, and US patent pending. BIV201 also has an Orphan Drug designation for the treatment of hepatorenal syndrome (HRS). The active agent in BIV201, terlipressin, is approved for use in about 40 countries for the treatment of related complications of advanced liver cirrhosis but is not available in the US or Japan. The FDA has never approved terlipressin. BioVie is targeting this landmark achievement.
One in 8 U.S. women will develop invasive breast cancer over her lifetime, with approximately 266,000 new breast cancer patients and 3.1 million breast cancer survivors in 2018. Following breast cancer surgery in the adjuvant setting, a HER2/neu 3+ patient typically receives Herceptin® in the first year, with the hope that their breast cancer will not recur, and with the odds of recurrence slowly decreasing over the first 5 years after surgery. Herceptin® has been shown to reduce recurrence rates from 25% to 12% in the adjuvant setting. In the neoadjuvant setting, a patient receives treatment before surgery and based on the results of a biopsy at surgery, will receive the same or more potent treatment after surgery. Kadcyla® has been shown to reduce recurrence rates from 22% to 11% in the neoadjuvant setting. Accordingly, we believe that GP2 may be used to address the 50% of recurring patients who do not respond to either Herceptin® or Kadcyla®.
Safer Technologies Program for Medical DevicesEMMAIntl
FDA has introduced a new program for medical devices and for device led combination products. Under this program are devices that do not qualify to be cleared via the breakthrough program but significantly improve the safety of the currently available options that treat diseases that are non-life threatening...
Lantern Pharma is a clinical stage biotechnology company focused on leveraging artificial intelligence (“A.I.”), machine learning and genomic date to streamline the drug development process and to identify patients who will benefit from their targeted oncology therapies. Their portfolio of therapies consists of compounds that others have tried, but failed, to develop into an approved commercialized drug. Additionally, they develop new compounds with the assistance of their A.I. platform (RADR) and biomarker driven approach. The Company is currently developing four therapeutic programs.
SciSparc is a specialty pharmaceutical company developing unique cannabinoid technologies for treatment of central nervous system disorders. The proprietary compounds capitalize on the biochemistry of receptors that specialize in modulating the central nervous system (CNS) to create therapeutics that mitigate the adverse symptoms associated with CNS disorders.
Cidara is developing long-acting therapeutics designed to improve the standard of care for patients facing serious diseases. The Company’s portfolio is comprised of drug candidates intended to transform existing treatment and prevention paradigms. Its lead Phase 3 antifungal candidate, rezafungin, will report Phase 3 data at the end of 2021. The potential peak sales opportunity for rezafungin in the US is ~$750M. In addition, the Company is developing Drug-Fc Conjugates (DFCs) targeting viral and oncology diseases from Cidara’s proprietary Cloudbreak® platform.
Second Sight Medical Products, a recognized global leader in neuromodulation devices for blindness, announced a definitive agreement on February 7, 2022, under which privately held Nano Precision Medical (NPM) will merge with a wholly owned subsidiary of Second Sight in an all-stock transaction. NPM will be the surviving company and owned by Second Sight. The resulting company will focus on development of innovative drug and device medical implants that treat chronic diseases with high unmet medical need.
Exact Sciences chairman and CEO Kevin Conroy delivered the company's presentation at the 2015 Baird 2015 Healthcare Conference in New York at 9:40 a.m. ET on Wednesday, Sept. 9.
An archive of the webcast is available here: http://wsw.com/webcast/baird43/register.aspx?conf=baird43&page=exas&url=http://wsw.com/webcast/baird43/exas/index.aspx
Nemaura Medical 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 as a general wellness product as part of its BEAT®diabetes program that is currently undergoing pilot studies.
Nemaura Medical is developing non-invasive and minimally invasive wearable diagnostic devices,
coupled with artificial intelligence capabilities for digital healthcare. The company’s first product,
which is CE approved and undergoing commercial launch, is the sugarBEAT® non-invasive
continuous glucose monitoring device and BEAT®diabetes digital healthcare platform.
sugarBEAT® 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 help people with Type 1 or Type 2 diabetes and prediabetes respectively to better manage,
reverse and prevent the onset of diabetes. BEAT®diabetes is a health subscription service
providing 1-on-1 lifestyle coaching and behavior change recommendations driven by personalized
data provided by sugarBEAT®. Insulin users can also adjunctively use sugarBEAT® for insulin
dosage purposes when calibrated by a finger stick reading. sugarBEAT® is intended to be worn
during waking hours and consists of a daily disposable adhesive skin-patch connected to a
rechargeable transmitter, with an app displaying glucose readings at five-minute intervals.
Nemaura Medical is developing non-invasive and minimally invasive wearable diagnostic devices,
coupled with artificial intelligence capabilities for digital healthcare. The company’s first product,
which is CE approved and undergoing commercial launch, is the sugarBEAT® non-invasive
continuous glucose monitoring device and BEAT®diabetes digital healthcare platform.
sugarBEAT® 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 help people with Type 1 or Type 2 diabetes and prediabetes respectively to better manage,
reverse and prevent the onset of diabetes. BEAT®diabetes is a health subscription service
providing 1-on-1 lifestyle coaching and behavior change recommendations driven by personalized
data provided by sugarBEAT®. Insulin users can also adjunctively use sugarBEAT® for insulin
dosage purposes when calibrated by a finger stick reading. sugarBEAT® is intended to be worn
during waking hours and consists of a daily disposable adhesive skin-patch connected to a
rechargeable transmitter, with an app displaying glucose readings at five-minute intervals.
Smart Blood Sugar builds upon the foundation of CGM technology and takes diabetes management a step further. It encompasses not only real-time glucose monitoring but also integrates advanced algorithms and data analytics to provide actionable insights and personalized recommendations.
The GlucoTru formula has been tested over 300 different ways to produce the greatest result and that is why we recommend you take GlucoTru every morning with breakfast.
By taking it in the morning you allow your body an all-day timed release of this incredible formula which will immediately start working to lower your blood sugar, burn fat and give you more energy.
GlucoTru works and here's why…
GlucoTru is the world's first 100% natural solution to wake up and activate the newly discovered “sleeper” hormone known as betatrophin laying dormant in your pancreas right now; The newly discovered, scientifically proven, root cause of your uncontrollable blood sugar, broken metabolism, and low energy levels.
Proven to be 233% more effective at lowering blood sugar and igniting your metabolism than any of the most popular medications or supplements on the planet!
Nemaura Medical (NASDAQ: NMRD)
Nemaura Medical (NASDAQ: NMRD), a medical technology company developing sugarBEAT® as a non-invasive affordable and flexible Continuous Glucose Monitor (CGM) for use by persons with diabetes and pre-diabetic
Managing blood sugar levels is crucial for overall health, particularly for individuals living with diabetes or those at risk of developing the condition. The ability to monitor blood sugar effectively empowers individuals to make informed decisions about their lifestyle, diet, and medical treatment. However, navigating the world of blood sugar monitoring can be overwhelming with the plethora of devices, techniques, and information available.
This comprehensive guide aims to demystify the process of blood sugar monitoring, providing essential knowledge and practical advice for anyone seeking to understand and manage their blood sugar levels effectively. Whether you're newly diagnosed with diabetes, caring for a loved one, or simply interested in optimizing your health, this guide will serve as a valuable resource.
In this guide, we'll delve into the fundamentals of blood sugar, explore different types of blood sugar monitors, offer guidance on choosing the right device, and provide step-by-step instructions for accurate monitoring. We'll also discuss how to interpret blood sugar readings, offer tips for maintaining optimal blood sugar levels, and explore advanced monitoring techniques and emerging trends in the field.
Additionally, we'll address specific challenges associated with blood sugar monitoring, such as emotional impacts, adherence issues, and overcoming obstacles in day-to-day management. Throughout the guide, we'll provide practical tips, insights from experts, and resources to support you on your journey towards better blood sugar control and overall well-being.
By understanding the principles of blood sugar monitoring and adopting effective strategies, you can take charge of your health and minimize the risks associated with fluctuating blood sugar levels. Let this guide be your companion in navigating the world of blood sugar monitoring, empowering you to live your best, healthiest life.
GCC Health 2.0: Tackling diabetes and obesity in an age of digital acceleration is a report by The Economist Intelligence Unit (EIU), sponsored by EY. It explores the role of technology in preventing and managing diabetes and obesity in the Gulf Co-operation Council (GCC) countries, highlighting the
potential impact on patients and the healthcare system.
Today developments in the healthcare industry, especially the integration of Artificial Intelligence (AI), have revolutionised the future of diabetes treatment. As technology and research continue to progress, it shows clearly that the future of diabetes is now.
The application of AI to diabetes treatment and management has been one of the key advancements that have molded the future of diabetes treatment in today’s time
The future of diabetes treatment is indeed promising and we can expect more and more innovations coming into existence. Scientists are already speculating about the involvement of nanotechnology in the future of diabetes research.
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2. Forward Looking
Statements
This presentation includes forward-looking statements that are subject to many risks and
uncertainties. These forward-looking statements, such as statements about Nemaura’s short-term
and long-term growth strategies, can sometimes be identified by use of terms such as “intend,”
“expect,” “plan,” “estimate,” “future,” “strive,” and similar words. These statements involve many
risks and uncertainties that may cause actual results to differ from what may be expressed or
implied in these statements.
These risks are discussed in Nemaura’s filings with the Securities and Exchange Commission (the
“Commission”), including the risks identified under the section captioned “Risk Factors” in
Nemaura’s Annual Report on Form 10-K filed with the Commission in June 2019 as the same may be
updated from time to time.
Nemaura disclaims any obligation to update information contained in these
forward-looking statements whether as a result of new information, future events, or otherwise.
3. Introduction
We developed the world’s first Daily-Wear non-invasive
Continuous Glucose Monitor (CGM) – A Class 2b CE
approved Medical Device.
Launched: sugarBEAT® and BEAT®diabetes, supporting
Diabetes prevention, management and reversal.
Planned Launch in 2021: Mass Market consumer metabolic
health App & Glucose Sensor Kit
4. The Problem…
There are over 463 million people living with diabetes worldwide,
and over $760 Billion was spent in the US alone in 2019 for
diabetes related healthcare expenditure1.
The total addressable market exceeds $150
Billion2,3,4.
Obesity and Diabetes are two of the major drivers of the
chronic disease epidemic
6. UNIQUE
The world’s first daily wear CGM: no
other sensor technology is currently
available allowing non-invasive daily
use.
LIFESTYLE
Other competing sensors are
worn for 10 - 14 days
consecutively. Nemaura’s BEAT®
sensors are designed for daily use
– any day you choose.
Our Unique Solution
KNOWLEDGE
Glucose sensors based on sugarBEAT provide guidance and
insights into the extent of control over sugar levels.
ENGAGEMENT
A world class digital program [and ecosystem] keeping the user
engaged for the long term.
OUTCOME
We expect the following based on independently published
reports using similar programs: improvements in HbA1C, blood
cholesterol, blood pressure, and sustainable weight loss. Real
results. Sustainable. Affordable.
7. Our Approach
1. sugarBEAT® CGM – real time glucose monitoring.
2. BEAT® diabetes – Digital program for diabetes
management and reversal, with intermittent glucose
profiling.
3. Mass market consumer metabolic health App and
Glucose Sensor Kit, targeting obesity, pre-diabetes
and Type 2 diabetes.
8. Total Addressable Market
UK
4.8 million people with diabetes8
One person diagnosed every 2
minutes
Germany
9.5 million have diabetes9.
4.5 million of these 9.5 million are
undiagnosed and, as a result, may
be particularly at risk.
U.S.
34.2 million have diabetes6
88 million people have pre-
diabetes
28,000 people diagnosed with diabetes EVERY WEEK
in the U.S. alone7 in a market worth nearly $150B
9. Impact on Healthcare Cost
q Healthcare costs for persons with type 2 diabetes cost approximately 2.5x as much as a person without diabetes. If
they experience complications, that number soars even higher10
q Employers and healthcare insurers are therefor resorting to programs that will provide long-term sustainable
results in stemming the onset of diabetes and, where possible, reversing Type 2 diabetes
q Current programs are cost prohibitive, but Nemaura has both a cost advantage as well as user friendliness from its
intermittent use sensors and will focus its efforts on the U.S. and European markets initially, for diabetes
prevention, management and potential reversal
healthy1 diabetes with complications
$
spent
per
year
$4k
diabetes
$12k
$21k
11. CE approved Class IIB
Medical Device
US FDA PMA approval
and launch in the US
anticipated by end of
2021
12. CE approved Class IIB
Medical Device
US FDA PMA approval
and launch in the US
anticipated by end of
2021
The world’s first daily wearable
Continuous Glucose Monitor that
doesn’t use needles.
CE Approved Class IIb Medical
Device
16. Why is sugarBEAT® Different?
User does not insert a 1cm long Filament in the arm using a large needle (like competing invasive
sensors) and keep it there for 10-15 days. The sensor sits on top of the arm/skin like a band aid.
User does not keep the sensor on the skin for 10-14 days, the sensor is a daily wear sensor – can
be worn during the day or at night, and sensor is thrown away each day.
Persons with Obesity, pre-diabetes or Type 2 generally would only need to wear a sensor a few
days a month. sugarBEAT® sensor allows flexible wear on demand, something that no other sensor
can currently offer.
A user pays for only those days of sensor wear they intend, and not 10-15 days by default,
therefore substantially reducing the monthly cost of sensors, yet providing the user with glucose
profile data that acts as a powerful tool to help users manage their health.
17. sugarBEAT® and Time in Range
A critical advantage of CGM-based systems is the ability to measure
the time that glucose levels are in normal range – i.e., time in range
(TIR). Control over TIR leads to a significant reduction in the onset of
complications of diabetes.
The same HbA1C values can give vastly differing TIR profiles and is
inferior to using CGM to measure TIR to prevent the onset of long-
term disease complications.
18. sugarBEAT® vs. HbA1C
40%
high
range
40%
in range
20%
low range
70%
high
range
25%
in range
5%
low
range
100%
in range
The same HbA1C value, yet 3 completely different TIR profiles, demonstrating the
power of TIR over HbA1C as the new gold standard11
19. sugarBEAT® Testimonials*
My Sugar Watch offered me a
needle-free blood glucose
monitoring solution that’s non-
invasive and easy to use. I didn’t
even realize I had the My Sugar
watch device on my arm as it is so
lightweight. It gives me the
assurance that my blood sugar
reading is accurate, and I have
access to my levels on my phone at
all times.
I was diagnosed with gestational
diabetes, and I was informed by my
healthcare professional that this may
lead to a diagnosis of Type 2 diabetes
in the future. Unfortunately, I was
diagnosed with Type 2 diabetes after
this and I have to manage this
diagnosis all by myself and learn to
control my blood glucose levels. Using
My Sugar Watch has alerted me to
changes in my blood glucose levels
and helped me understand how these
changes make an impact on my body
and how I am feeling. To have this
information at my fingertips gives me
so much control to manage my
diabetes.
I have been a Type 2 diabetic for 10
years. I sporadically manage my
blood sugar with a blood glucose
monitoring device. I know that if
not controlled or managed
effectively I can have real highs and
lows and not know when this will
happen. I was wearing the My
Sugar Watch device and it alerted
me to the fact I was about to have a
hypo before it happened. This alert
enabled me to quickly balance my
medication.
*UK Licensee users’ feedback
20. sugarBEAT®
Sales status UK
uUK: 200,000 Sensors ordered by licensee following soft launch
success
uPurchase order forecast for (approximately) a further 100,000
sensors per month for the next 2 years, totaling over 2 million
sensors.
uLicensee selling these based on a diabetes management subscription
service.
21. sugarBEAT®
Germany
uPartnership/Collaboration discussions ongoing
uSubmission for reimbursement made to GBA, the German Regulatory
Authority. GBA confirmed they do not need to review this and it is now
progressing straight to the National Association of Statutory Health Insurance
Funds, thus we expect the process to be a lot quicker.
uPlan to launch as soon as partnership agreement is signed.
24. Type 2 Diabetes prevention
and management program
launched in the U.S.
25. BEAT®diabetes – 3 Components
1. Weight loss program originally developed at the Joslin Diabetes Centre
– over 12 years of clinical evidence (based on an in-clinic program,
subsequently replicated using a virtual program). Sustained long term
weight loss achieved without loss of muscle mass
2. proBEAT™ Intermittent glucose profiling – using world’s first daily-
wearable glucose sensor, developed in-house
3. Coaching: digital 24/7 using app, and specialist 1 to 1 coaching
26. BEAT®diabetes – Glucose Profiling
Intermittent Glucose Profiling: Benefits
7-point glucose profiles every 4 weeks. Patients received
guidance for diet and exercise adjustments based on SMBG.
Outcome: Significant reductions in HbA1c, weight, BMI, systolic
BP, diastolic BP, and LDL Cholesterol
Kempf et. al., Diabetes Technol Ther (2010)
27. BEAT®diabetes
Potential Outcome for Payers
Healthier Employees = Healthier Business
$1,600
$4,700
$6,600
$9,100
Healthy (No
conditions)
Prediabetes only Hypertension Only Diabetes Only
Annual Cost per Employee
On average, diabetes costs both employers
and insurers over $9,000 per year. Potential
savings from prescription medications
alone would amount to over $5,000 per
year.
28. BEAT®diabetes
Current Status
uFirst Pilot Commenced, with approx. 200 participants
planned for a program of up to 2 years.
uAnticipate multiple parallel additional pilots in near
term
29. BEAT Metabolic Health
Metabolism is life.
Can we help 87 MILLION people in the USA
from becoming Diabetic using our
low cost wearable glucose sensor and digital ecosystem?
30. Metabolic Health
A mass-market consumer product
A new program leveraging off the BEAT® wearable sensor platform to address improvements in metabolic
health and well-being. Launching in 2021. Applicable to over 80 million people in the US with pre-diabetes as
well as general health-conscious individuals, and obesity market.
31. CONTINUOUS LACTATE MONITORING
Assists in threshold maximization in
performance athletes
Early identification of tissue hypoperfusion or
shock for aggressive early resuscitation of
critically ill patients to improve the their
chances of survival
BODY TEMPERATURE MONITORING
Gives a more accurate and large data set. For
monitoring viral infections and lower limb blood
circulation tracking the effectiveness of drugs
Wearable temperature sensors market is expected
to register a CAGR of 8.3% during the forecast
period 2021-202622
Future Product Opportunities
Leveraging the BEAT® Technology
A rich portfolio of additional products to complement existing offering and contribute to increased
revenues
32. ALCOHOL MONITORING
Support personal health goals and provide
warnings prior to driving.
Provide physicians with individual’s drinking
habits.
Prevention of progression-to-alcohol-related
disease
DRUG MONITORING
Monitoring the impact of drugs and personalized
treatment plan for patients.
Global therapeutic drug monitoring device market
to reach $3.37B by 202423
Future Product Opportunities
Leveraging the BEAT® Technology
33. BIG DATA
Predictive analytics based on logic drawn from wearable
medical devices using algorithms to seek patterns and
structure in data and cluster them into groups or insights.
Improving efficiencies per patient’s management of health
care. Accuracy of diagnosis and treatment in personal
medicine.
ARTIFICIAL INTELLIGENCE
Empowering users & industry with interpretations of
SugarBEAT® data to enhance treatment & develop
personalized therapy
The U.S. National Institutes of Health is working with
IBM to connect a wide variety of clinical and research
datasets to the IBM Watson system.
BigDataisprojectedtohavesignificantapplicationsthehealthcaretechspace.
Themarketisexpectedtogrowtoover$68Billionby202424
Future Product Opportunities
Leveraging the BEAT® Technology
34. The Team
uWe are building a world class team
uSo far includes senior level appointments, with
experience from companies including: Dexcom,
Lifescan, Roche, Abbvie, & Eli Lilly
35. Intellectual
Property
q Nemaura is building an extensive and
valuable intellectual property portfolio to
position the company to become a global
leader in the non-invasive wearable sensor
market.
q Nemaura has over 30 patents across several
patent families (both approved and
pending), and substantial trade secrets,
providing a strong IP position.
q Nemaura anticipates filing multiple
additional patents over the course of the
next 18 months, based on ongoing
developments.
1. Sensor related
2. Algorithm and methods of
using the CGM data
3. Devices & methods to
enhance glucose sensing
4. Methods to enhance
glucose sensing
5. Devices and methods to
extract glucose
The Company has a number of patent families and trade
secrets spanning the following:
36. Future Milestones
We expect to report the following over the coming months:
- Progress with sales of sugarBEAT® in multiple territories
- Commencement of KOL studies in the UK and USA
- Launch of the Metabolic Health App & Sensor Kit
- Adoption of BEAT®diabetes program/pilot studies in the USA
- Update on FDA PMA application for sugarBEAT®
37. Cash Position
As of 26th July 2021:
Strong balance sheet (>$30M, and <$2M quarterly cash burn)