Valbiotis Announces Positive Preclinical Results for TOTUM•070 in Hypercholesterolemia, Selected and Presented at the American Heart Association (AHA) Annual Meeting
Regulatory News:
This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20211114005021/en/
TOTUM•070 preclinical results AHA 2021 (Graphic: Valbiotis)
Valbiotis (Paris:ALVAL) (FR0013254851 – ALVAL, PEA / SME eligible), a Research and Development company committed to scientific innovation for preventing and combating metabolic diseases, announces the selection of TOTUM•070's positive preclinical results in hypercholesterolemia by the annual meeting of the American Heart Association, the leading American learned society in the cardiovascular field.
Valbiotis is presenting two posters on TOTUM•070 at the AHA meeting, which is being held November 13-15, 2021, in virtual format. The results presented show a significant reduction in total cholesterol and particularly "bad" cholesterol (including LDL cholesterol)*, as well as initial data in favor of a multi-target mode of action on lipid metabolism. They support the potential of TOTUM•070, currently in Phase II of its clinical development against hypercholesterolemia. Recruitment has been completed and results are expected in the second quarter of 2022, with LDL cholesterol reduction as the primary endpoint.
TOTUM•070 is an innovative active substance based on a combination of 5 plant extracts (without phytosterols or red yeast rice), designed to reduce LDL cholesterol, a cardiovascular risk factor and the primary cause of atherosclerosis. It is developed for people with mild to moderate, untreated hypercholesterolemia.
The two studies presented at the AHA congress confirm the efficacy of TOTUM•070 on cholesterol and blood lipids and provide initial data on the mode of action of this active substance. In the two in vivo models explored, the work demonstrates that TOTUM•070 largely prevents hypercholesterolemia, with a dose-dependent reduction in "bad" cholesterol* of up to 47%. The first data on mode of action also reveal significant effects on several key mechanisms for the regulation of lipid metabolism, notably intestinal, hepatic and inflammatory.
This in-depth work is the result of close cooperation between Valbiotis' preclinical platform in Riom (Puy de Dôme) and Bruno GUIGAS' team at the University of Leiden (Netherlands), one of the Company's longstanding academic partners.
Pascal SIRVENT, Director of Discovery, Preclinical and Translational Research, member of the Valbiotis Board of Directors, comments: "These results on TOTUM•070 are striking in their consistency. First, they confirm a strong and dose-dependent preventive effect on blood cholesterol, the ultimate target of this active substance. Furthermore, they confirm the hypothesis of a multi-target mode of action on the regulation of lipid metabolism, a central objective of our plant-based approach. This is an important data set for the development and future commercialization of TOTUM•070 in hypercholesterolemia and a very promising signal for ongoing clinical studies. Their selection by the American Heart Association Congress is of course a great source of pride and recognition of the quality of the work done by our teams and those of the University of Leiden."
Bruno GUIGAS, Assistant Professor at the University of Leiden (Netherlands), adds:
"This research project had an exciting overall ambition for TOTUM•070, for the prevention of hypercholesterolemia. For our part, we focused on the intestinal mode of action of this active substance and demonstrated a significant effect on fat absorption. This is a particularly positive result on this well-known lever of lipid metabolism regulation. As an R&D partner of Valbiotis since 2015, we are very pleased with our contribution to the success of these joint projects, whose benefits and value are clearly demonstrated through their selection by the AHA Congress."
TOTUM•070 efficacy and mode of action results presented at AHA 2021
Both studies were conducted in two in vivo models, predictive of human pathophysiology, where hypercholesterolemia was induced by a high-fat diet. TOTUM•070 was administered according to a prevention protocol together with the high-fat diet. The design included two controls: one with a high-fat diet alone and the other with a normal diet. The first study was mainly oriented to efficacy objectives and tested TOTUM•070 at three different doses for 12 weeks. The second study, oriented to mode of action hypotheses, tested 2 different doses for 6 weeks. In both protocols, the results show a significant reduction of cholesterol levels by TOTUM•070 compared to a high-fat diet alone, confirming the preventive effect sought with this active substance.
The first study demonstrates a profound efficacy of TOTUM•070 on circulating lipids, with a dose-dependent reduction of 37-48% of "bad" cholesterol (non-HDL)*, 31-42% of total cholesterol as well as 30-46% of blood triglycerides, compared to the high-fat diet alone, after 12 weeks.
In terms of mode of action, the second study provided exploratory data indicating two major effects of TOTUM•070: reduction of intestinal absorption of lipids and reduction of their accumulation in the liver.
In both models, gene expression analyses also showed that TOTUM•070 administration normalized many markers involved in lipid metabolism as well as some pro-inflammatory markers, whereas they were strongly altered by a high-fat diet alone.
Link to the posters: https://www.valbiotis.com/en/publications/
About TOTUM•070
TOTUM•070 is an innovative active substance derived from food plant extracts, without phytosterols or red yeast rice, developed to act on lipid metabolism in people with hypercholesterolemia.
TOTUM•070 is currently being tested in a Phase II clinical trial, the HEART study, an international, multi-center, randomized, placebo-controlled study on 120 volunteers with mild to moderate hypercholesterolemia. Enrolment in this study was completed in September 2021 and results are expected in the second quarter of 2022.
At the end of its development, this new Health Nutrition product will be positioned in particular in people with LDL hypercholesterolemia, for levels up to 190 mg/dl, with a moderate overall cardiovascular risk. TOTUM•070 could be recommended to this large population for whom no drug therapy is currently recommended as first-line treatment, with the objective of reducing LDL cholesterol levels and thus the overall cardiovascular risk.
About Valbiotis
Valbiotis is a Research & Development company committed to scientific innovation for preventing and combating metabolic diseases in response to unmet medical needs.
Valbiotis has adopted an innovative approach, aiming to revolutionize healthcare by developing a new class of health nutrition products designed to reduce the risk of major metabolic diseases, relying on a multi-target strategy enabled by the use of plant-based terrestrial and marine resources.
Its products are intended to be licensed to players in the health sector.
Created at the beginning of 2014 in La Rochelle, the Company has forged numerous partnerships with leading academic centers. The Company has established three sites in France – Périgny, La Rochelle (17) and Riom (63) – and a subsidiary in Quebec City (Canada).
Valbiotis is a member of the "BPI Excellence" network and has been recognized as an "Innovative Company" by the BPI label. Valbiotis has also been awarded "Young Innovative Company" status and has received major financial support from the European Union for its research programs via the European Regional Development Fund (ERDF). Valbiotis is a PEA-SME eligible company.
For more information about Valbiotis, please visit: www.valbiotis.com
Name: Valbiotis
ISIN code: FR0013254851
Ticker symbol: ALVAL
EnterNext© PEA-PME 150
1"Bad" cholesterol is the non-HDL fraction of cholesterol. It includes ApoB lipoproteins, i.e. VLDL and LDL cholesterol.
This press release contains forward-looking statements about Valbiotis’ objectives. Valbiotis considers that these projections are based on rational hypotheses and the information available to Valbiotis at the present time. However, in no way does this constitute a guarantee of future performance, and these projections may be affected by changes in economic conditions and financial markets, as well as certain risks and uncertainties, including those described in the Valbiotis Universal Registration Document approved by the French Financial Markets Regulator (AMF) on July 27, 2021 (application number R 21-039). This document is available on the Company’s website ( www.valbiotis.com).
This press release and the information it contains do not constitute an offer to sell or subscribe, or a solicitation to purchase or subscribe to Valbiotis’ shares or financial securities in any country.
To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.
View source version on businesswire.com: https://www.businesswire.com/news/home/20211114005021/en/
Contact information
Corporate communication / Valbiotis
Carole Rocher / Marc Delaunay
+33 5 46 28 62 58
media@valbiotis.com
Financial communication / Actifin
Stéphane Ruiz
+33 1 56 88 11 14
sruiz@actifin.fr
About Business Wire
For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Dompé's Program in NAION Selected for Landmark FDA Commissioner’s National Priority Voucher Program17.10.2025 03:42:00 EEST | Press release
Dompé, a leading biopharmaceutical company with operations in Italy and the US, announced today its selection by the United States Food and Drug Administration (FDA) to participate in the Commissioner’s National Priority Voucher (CNPV) program. Because of its selection, Dompé has been awarded a voucher granting a significantly shortened review timeline for marketing application and enhanced collaboration with the FDA. Dompé intends to apply the voucher for the Biologic License Application (BLA) for an intranasally administered formulation of Nerve Growth Factor (Cenegermin-bkbj) for the treatment of non-arteritic anterior ischemic optic neuropathy (NAION). The intranasal administration of NGF is a novel approach, patented by Dompé, offering a non-invasive delivery method. “The CNPV represents a strategic lever to accelerate access to transformative therapies for patients with unmet medical needs as NAION,” said Sergio Dompé, Executive President at Dompé. “Building on our pioneering ach
Bentley Systems Announces Winners of the 2025 Going Digital Awards17.10.2025 02:00:00 EEST | Press release
(Bentley Systems’ Year in Infrastructure 2025) – Bentley Systems, Incorporated (Nasdaq: BSY), the infrastructure engineering software company, today announced the winners of the 2025 Going Digital Awards. The annual awards honor the extraordinary work of infrastructure professionals and their innovative use of Bentley software to improve the way infrastructure is designed, built, and operated. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251016841527/en/ Bentley Systems announced the winners of the 2025 Going Digital Awards on October 16, 2025 (Photo courtesy of Bentley Systems) This year, nearly 250 projects were nominated by organizations in 47 countries. Winners were selected across 12 categories by a panel of independent judges during Bentley’s Year in Infrastructure conference, held October 15-16 in Amsterdam. “Congratulations to this year’s Going Digital Award winners,” said Chris Bradshaw, chief sustainability and e
Kinaxis Inc. to Host Third Quarter 2025 Financial Results Conference Call on November 6, 202517.10.2025 00:00:00 EEST | Press release
Kinaxis® Inc. (TSX:KXS), a global leader in end-to-end supply chain orchestration, today announced that it has scheduled its conference call to discuss the financial results for its third quarter ended September 30, 2025. The call will be hosted on Thursday, November 6 at 8:30 a.m. Eastern Time by Bob Courteau, interim chief executive officer and chair, and Blaine Fitzgerald, chief financial officer, followed by a question and answer period. The Company will report its financial results for the third quarter after the close of markets on Wednesday, November 5, 2025. CONFERENCE CALL DETAILS DATE: Thursday, November 6, 2025 TIME: 8:30 a.m. Eastern Time CALL REGISTRATION:https://registrations.events/direct/Q4I91416498WEBCAST:https://events.q4inc.com/attendee/875765587 (available for three months) Advance call registration Participants must register in advance for the live call. After registering, instructions on how to join the call will automatically be emailed, including dial-in informa
HCLTech and Zscaler Expand Partnership for AI-Powered Security and Network Transformation16.10.2025 21:13:00 EEST | Press release
HCLTech, a leading global technology company, and Zscaler™, a leader in cloud security, announced the expansion of their strategic partnership to provide AI-powered network transformation and enhanced zero-trust security services to enterprises worldwide. Under the new partnership scope, Zscaler's Zero Trust Exchange™ platform has been integrated with HCLTech's Cybersecurity Fusion Center (CSFC) platform. HCLTech’s AI capabilities, including SecOps and Responsible AI guardrails within HCLTech AI Force and AI Foundry are key to this partnership. This collaboration aims to enhance enterprise resilience and achieve business outcomes with a cloud-first, scalable security solution. HCLTech's Universal Managed Detection and Response (UMDR) services now integrate with Zscaler Internet Access™ (ZIA™), Zscaler Private Access™ (ZPA™) and other Zscaler components, providing context-rich threat detection, advanced analytics and faster response powered by AI and automation. Other key highlights of
Beyon Cyber and Haven Sign MoU to Launch Advanced AI-Powered SOC Capabilities in the UK and Worldwide16.10.2025 20:58:00 EEST | Press release
Beyon Cyber, part of the Beyon Group and the fastest growing cyber security company in the Middle East, has signed a Memorandum of Understanding (MoU) with Haven Cyber Technologies, a global cyber security services provider and a Microsoft Solutions Partner, through its UK-based subsidiary ITC Secure. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251016047852/en/ Beyon Cyber and Haven Sign MoU Under the MoU, Beyon Cyber and Haven will form a strategic partnership to revolutionize cyber security operations through the launch of advanced AI-driven Security Operations Centers (AI SOCs) in the United Kingdom and worldwide. As part of this collaboration, Haven will integrate Beyon Cyber’s cutting-edge AI SOC platform, Orryx AI, into its operations; harnessing the power of smart automation and agentic AI workflows to enhance threat detection, investigation, hunting, intelligence, and response. This partnership will enable both or
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom