Sorbitol

Applied Therapeutics Reports Fourth Quarter and Year-end 2023 Financial Results

Retrieved on: 
Wednesday, March 6, 2024

The FDA also noted that it is planning to hold an advisory committee meeting to discuss the application.

Key Points: 
  • The FDA also noted that it is planning to hold an advisory committee meeting to discuss the application.
  • Govorestat was previously granted Pediatric Rare Disease designation and will qualify for a Priority Review Voucher (PRV) upon approval.
  • The Company expects a decision by the EMA in the fourth quarter of 2024.
  • Full study results will be presented at an upcoming medical conference, along with results of the Diabetic Peripheral Neuropathy sub-study, which are still being analyzed.

Tate & Lyle Partners with Cryptobiotix: New ex-vivo study on low and no calorie sweeteners finds positive impact or no impact on human gut microbiota

Retrieved on: 
Thursday, February 15, 2024

Tate & Lyle PLC (Tate & Lyle), a world leader in ingredient solutions for healthier food and drink, partnered with Cryptobiotix, pioneers in preclinical gastrointestinal research, on the study.

Key Points: 
  • Tate & Lyle PLC (Tate & Lyle), a world leader in ingredient solutions for healthier food and drink, partnered with Cryptobiotix, pioneers in preclinical gastrointestinal research, on the study.
  • The doses of low and no calorie sweeteners used were based on actual intakes, regulations and amounts that are generally included in foods and beverages during different timepoints.
  • Assessments of additional low and no calorie sweeteners, including allulose and erythritol, are being completed and details will be shared in due course.
  • The low and no calorie sweeteners studied for this paper included: Acesulfame potassium (aceK), maltitol, sorbitol, stevia, sucralose and tagatose.

Applied Therapeutics Announces Positive Results from 12-month Interim Analysis of Govorestat (AT-007) in the Ongoing INSPIRE Phase 3 Trial in Sorbitol Dehydrogenase (SORD) Deficiency

Retrieved on: 
Thursday, February 15, 2024

The INSPIRE trial is a Phase 3 double-blind placebo-controlled registrational study evaluating the effect of once-daily (QD) oral govorestat (AT-007) in 56 patients aged 16-55 with SORD Deficiency in the US and Europe.

Key Points: 
  • The INSPIRE trial is a Phase 3 double-blind placebo-controlled registrational study evaluating the effect of once-daily (QD) oral govorestat (AT-007) in 56 patients aged 16-55 with SORD Deficiency in the US and Europe.
  • Govorestat is a central nervous system penetrant Aldose Reductase Inhibitor, which blocks the conversion of glucose to sorbitol, and has previously been shown to reduce sorbitol levels in patients with SORD Deficiency.
  • We believe the results from the 12-month interim analysis confirm the role of sorbitol as a key driver of disease severity and progression over time.
  • A replay of the webcast will be available for 90 days on the Investors section of Applied Therapeutics’ website.

New ex-vivo study on low and no calorie sweeteners finds positive impact or no impact on human gut microbiota

Retrieved on: 
Thursday, February 8, 2024

Tate & Lyle and Cryptobiotix's breakthrough ex-vivo* study shows that sucralose does not impact the gut microbiota, while other low and no calorie sweeteners have potentially beneficial health effects

Key Points: 
  • Tate & Lyle and Cryptobiotix's breakthrough ex-vivo* study shows that sucralose does not impact the gut microbiota, while other low and no calorie sweeteners have potentially beneficial health effects
    LONDON, Feb. 8, 2024 /PRNewswire/ - A new, first-of-its-kind study has identified unique and potentially beneficial interactions between certain low and no calorie sweeteners, including stevia, and the human gut microbiota.
  • The doses of low and no calorie sweeteners used were based on actual intakes, regulations and amounts that are generally included in foods and beverages during different timepoints.
  • Assessments of additional low and no calorie sweeteners, including allulose and erythritol, are being completed and details will be shared in due course.
  • The low and no calorie sweeteners studied for this paper included: Acesulfame potassium (aceK), maltitol, sorbitol, stevia, sucralose and tagatose.

Diabetic Tussin Reintroduces Sugar-Free Cold and Cough Solution for People with Diabetes

Retrieved on: 
Wednesday, November 29, 2023

TARRYTOWN, N.Y., Nov. 29, 2023 /PRNewswire/ -- Today, Diabetic Tussin®, the trusted cough syrup brand for people with diabetes and prediabetes, announces its sugar-free cold and cough solution is back on shelves. This restock brings with it the Better Choices for Life mark from the American Diabetes Association® (ADA). This over-the-counter cold and cough solution returns just as the threat of a 'tripledemic' — when cases of COVID-19, flu, and RSV surge at the same time—looms over American households.

Key Points: 
  • TARRYTOWN, N.Y., Nov. 29, 2023 /PRNewswire/ -- Today, Diabetic Tussin®, the trusted cough syrup brand for people with diabetes and prediabetes, announces its sugar-free cold and cough solution is back on shelves.
  • This over-the-counter cold and cough solution returns just as the threat of a 'tripledemic' — when cases of COVID-19, flu, and RSV surge at the same time—looms over American households.
  • "Diabetic Tussin is an essential over-the-counter cold and cough solution for millions of Americans concerned about ingredients in other products that can raise blood sugar levels.
  • Made with the strongest sugar-free formula on the market, Diabetic Tussin Max allows consumers to effectively manage their cough and cold symptoms with the right ingredients.

Global Polyol Sweeteners Strategic Market Report 2023: A $7.5+ Billion Market by 2030 - Focus on Sorbitol, Xylitol, Mannitol, Maltitol, Isomalt - ResearchAndMarkets.com

Retrieved on: 
Friday, September 15, 2023

The global market for Polyol Sweeteners is undergoing significant growth, with the industry expected to flourish in the coming years.

Key Points: 
  • The global market for Polyol Sweeteners is undergoing significant growth, with the industry expected to flourish in the coming years.
  • Independent analysis reveals substantial market potential across various geographic regions, offering valuable insights into past, present, and future trends.
  • With applications ranging from Food & Beverage to Personal Care & Cosmetics, Pharmaceuticals, and more, the Polyol Sweeteners market is poised for impressive growth.
  • The Polyol Sweeteners market in the U.S. is estimated at US$1.2 Billion in the year 2022.

Applied Therapeutics Reports Second Quarter 2023 Financial Results

Retrieved on: 
Thursday, August 10, 2023

NEW YORK, Aug. 10, 2023 (GLOBE NEWSWIRE) -- Applied Therapeutics, Inc. (Nasdaq: APLT), a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need, today reported financial results for the second quarter ended June 30, 2023.

Key Points: 
  • “In the second quarter we continued to advance our programs across Galactosemia, SORD Deficiency and Diabetic Cardiomyopathy,” said Shoshana Shendelman, PhD, Founder, Chief Executive Officer, and Chair of the Board.
  • In June 2023, the Company presented baseline data at the 2023 Annual Meeting of the ADA from the ongoing Phase 3 ARISE-HF study of AT-001 (caficrestat) in Diabetic Cardiomyopathy (DbCM).
  • The Company expects topline data from the study in the fourth quarter of 2023.
  • Net loss for the second quarter of 2023 was $29.6 million, or $0.37 per basic and diluted common share, compared to a net loss of $25.9 million, or $0.96 per basic and diluted common share, for the second quarter 2022.

WHO expert cancer group states that the sweetener aspartame is a possible carcinogen, but evidence is limited – 6 questions answered

Retrieved on: 
Friday, July 21, 2023

The World Health Organization declared on July 14, 2023, that the widely used synthetic sweetener aspartame could be a “possible” carcinogen, or cancer-causing agent, on the basis of “limited evidence for cancer in humans.” But the agency also concluded that the currently available data does not warrant a change of the acceptable daily intake of aspartame at this time.

Key Points: 
  • The World Health Organization declared on July 14, 2023, that the widely used synthetic sweetener aspartame could be a “possible” carcinogen, or cancer-causing agent, on the basis of “limited evidence for cancer in humans.” But the agency also concluded that the currently available data does not warrant a change of the acceptable daily intake of aspartame at this time.
  • The Conversation asked chronic disease epidemiologist Paul D. Terry, public health scholar Jiangang Chen and nutrition expert Ling Zhao, all from the University of Tennessee, to put these seemingly contradictory findings into perspective based on the available scientific evidence.

1. Why is aspartame being classified as ‘possibly’ cancer-causing?

    • Because it is approximately 200 times sweeter than table sugar, smaller amounts of aspartame are added to foods, and they contribute considerably fewer calories.
    • NutraSweet and Equal are well-known brand names for aspartame sold in packages for individual use.
    • The International Agency for Research on Cancer, an entity within the WHO, evaluated findings from both human and animal studies of aspartame and cancer.

2. What are the current guidelines for aspartame consumption?

    • This amount of aspartame per day translates to approximately eight to 12 cans of soda, or approximately 60 packets of aspartame, for a person weighing 132 pounds (60 kilograms).
    • For a child weighing 33 pounds (15 kg), it translates to between two to three cans of aspartame-sweetened soda per day, or approximately 15 packets of aspartame.

3. Does the WHO’s new stance change that recommendation?

    • Independently of the expert panel on cancer, the food safety group also evaluated the available evidence and concluded that there was no “convincing evidence” from either animal or human studies that aspartame consumption causes adverse effects within the currently established daily limits.
    • It is important to note that people with the rare inherited disorder called phenylketonuria, or PKU, should avoid or restrict aspartame intake.

4. How can two consensus groups reach different conclusions?

    • It is not uncommon for scientific consensus groups to differ in how they classify risk based on the results of published studies, even if more than one of those consensus groups is affiliated with the same agency or parent organization.
    • Whereas the WHO’s expert cancer group’s stance may appear to be more worrisome than that of the committee on food safety, in fact, the latter’s “no convincing evidence” is consistent with the cancer group’s “limited evidence” classification.

5. How does aspartame compare to other sweeteners?

    • But, like aspartame, many of these sweeteners have been implicated in developing cancer.
    • This list includes acesulfame potassium, or Ace-K – a synthetic calorie-free sugar substitute – as well as sugar alcohols and even simple sugar.

6. So what should consumers do?

    • And, as noted by the Mayo Clinic, artificial sweeteners may play a beneficial role for some people who are seeking to manage their weight or control their sugar intake.
    • One thing is clear: Scientific studies on aspartame consumption will continue, and it will be important for both consumers and the research community to continue weighing potential risks.

Applied Therapeutics to Present Data on AT-007 (Govorestat) Treatment in SORD Deficiency at the 2023 Annual Meeting of the Peripheral Nerve Society

Retrieved on: 
Thursday, June 15, 2023

Data further elucidates the pathophysiology of sorbitol toxicity, including sorbitol accumulation as the driver of disease in patient-derived motor neurons, as well as in the drosophila model and a new rat model of SORD Deficiency

Key Points: 
  • Data further elucidates the pathophysiology of sorbitol toxicity, including sorbitol accumulation as the driver of disease in patient-derived motor neurons, as well as in the drosophila model and a new rat model of SORD Deficiency
    Clinical study data includes trial design, baseline data and 3-month sorbitol reduction from the Phase 3 INSPIRE study in patients with SORD Deficiency
    NEW YORK, June 15, 2023 (GLOBE NEWSWIRE) -- Applied Therapeutics, Inc. (Nasdaq: APLT), a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need, today announced multiple oral presentations at the 2023 Annual Meeting of the Peripheral Nerve Society to take place June 17 - 20 in Copenhagen, Denmark.
  • Oral Presentation by Michael Shy, MD: Monday, June 19, 11:50 AM CEST
    Oral Presentation by Amanda Lobato: Monday, June 19, 12:35 PM CEST
    Oral Presentation by Adriana Rebelo, PhD: Tuesday, June 20, 9:30 AM CEST

METER Food Uncovers Major Findings Affecting Alternative Sweeteners Viability as Sugar Replacement

Retrieved on: 
Thursday, May 25, 2023

Pressure from consumers and governmental agencies to reduce the amount of sugar in foods has turned the sugar alternative industry into an $18 billion market.

Key Points: 
  • Pressure from consumers and governmental agencies to reduce the amount of sugar in foods has turned the sugar alternative industry into an $18 billion market.
  • “As demand for healthier snacks and treats continues to grow, innovative new sweeteners abound,” said Mary Galloway, METER Food R&D Lab Manager.
  • Simply put, replacing sugar seems simple, but it isn’t.”
    While alternative sweeteners make it possible to create sugar-free versions of old consumer favorites, there’s more to sugar and its substitutes than just taste.
  • Findings from study identifies the benefits and challenges with top alternative sweeteners and the scientific concepts that explain sugar’s unique characteristics.