-
Japan's only two pandas to be sent back to China
-
Zelensky, US envoys to push on with Ukraine talks in Berlin
-
Australia to toughen gun laws after deadly Bondi shootings
-
Lyon poised to bounce back after surprise Brisbane omission
-
Australia defends record on antisemitism after Bondi Beach attack
-
US police probe deaths of director Rob Reiner, wife as 'apparent homicide'
-
'Terrified' Sydney man misidentified as Bondi shooter
-
Cambodia says Thai air strikes hit home province of heritage temples
-
EU-Mercosur trade deal faces bumpy ride to finish line
-
Inside the mind of Tolkien illustrator John Howe
-
Mbeumo faces double Cameroon challenge at AFCON
-
Tongue replaces Atkinson in only England change for third Ashes Test
-
England's Brook vows to rein it in after 'shocking' Ashes shots
-
Bondi Beach gunmen had possible Islamic State links, says ABC
-
Lakers fend off Suns fightback, Hawks edge Sixers
-
Louvre trade unions to launch rolling strike
-
Far-right Kast wins Chile election landslide
-
Asian markets drop with Wall St as tech fears revive
-
North Korean leader's sister sports Chinese foldable phone
-
Iran's women bikers take the road despite legal, social obstacles
-
Civilians venture home after militia seizes DR Congo town
-
Countdown to disclosure: Epstein deadline tests US transparency
-
Desperate England looking for Ashes miracle in Adelaide
-
Far-right Kast wins Chile election in landslide
-
What we know about Australia's Bondi Beach attack
-
Witnesses tell of courage, panic in wake of Bondi Beach shootings
-
Chiefs out of playoffs after decade as Mahomes hurts knee
-
Chilean hard right victory stirs memories of dictatorship
-
Volunteers patrol Thai villages as artillery rains at Cambodia border
-
Apex Discovers Mineralized Carbonatite at its Lac Le Moyne Project, Québec
-
Lin Xiang Xiong Art Gallery Officially Opens
-
Fintravion Business Academy (FBA) Aligns Technology Development Strategy Around FintrionAI 6.0 Under Adrian T. Langshore
-
Pantheon Resources PLC - Retirement of Director
-
HyProMag USA Provides Positive Update to Valuation Of Expanded Dallas-Fort Worth Plant And Commences Strategic Review to Explore a U.S. Listing
-
Relief Therapeutics and NeuroX Complete Business Combination and Form MindMaze Therapeutics
-
Far-right candidate Kast wins Chile presidential election
-
Father and son gunmen kill 15 at Jewish festival on Australia's Bondi Beach
-
Rodrygo scrapes Real Madrid win at Alaves
-
Jimmy Lai, the Hong Kong media 'troublemaker' in Beijing's crosshairs
-
Hong Kong court to deliver verdicts on media mogul Jimmy Lai
-
Bills rein in Patriots as Chiefs eliminated
-
Chiefs eliminated from NFL playoff hunt after dominant decade
-
Far right eyes comeback as Chile presidential polls close
-
Freed Belarus dissident Bialiatski vows to keep resisting regime from exile
-
Americans Novak and Coughlin win PGA-LPGA pairs event
-
Zelensky, US envoys to push on with Ukraine talks in Berlin on Monday
-
Toulon edge out Bath as Saints, Bears and Quins run riot
-
Inter Milan go top in Italy as champions Napoli stumble
-
ECOWAS threatens 'targeted sanctions' over Guinea Bissau coup
-
World leaders express horror at Bondi beach shooting
One-Year Data from the VenoValve(R) U.S. Pivotal Trial Highlighting Impact on Patients' Quality of Life (QOL) to be Presented Today at the 37th Annual Meeting of the American Venous Forum
One-year follow-up data demonstrates sustained improvements across venous specific quality-of-life (QoL) indicators.
PMA application for the VenoValve submitted in November 2024, with an FDA decision expected in the second half of 2025.
IRVINE, CA / ACCESS Newswire / February 19, 2025 / enVVeno Medical Corporation (NASDAQ:NVNO) ("enVVeno" or the "Company"), a company setting new standards of care for the treatment of venous disease, today announced that one-year follow-up data on 75 subjects from the VenoValve U.S. pivotal trial will be presented by Dr. Cassius Iyad Ochoa Chaar, Associate Professor Surgery, Yale School of Medicine, Division of Vascular and Endovascular Surgery, Principal Investigator, and lead enroller for the trial, at the 37th Annual Meeting of the American Venous Forum (VENOUS2025) being held February 16-19, 2025 in Atlanta, GA. The presentation is scheduled for today at 9:47 AM ET.

The data show that trial subjects who had the SAVVE procedure experienced statistically significant improvements in QoL metrics related to venous disease at 12 months compared to baseline as demonstrated by the VEINS-SYM/QOL scores. To view results from the trial, please visit www.venovalve.com. The Company has submitted a pre-market authorization (PMA) application for the VenoValve to the U.S. Food and Drug Administration (FDA), with a decision anticipated in the second half of 2025.
"We continue to be asked to present our data at leading vascular conferences throughout the world as news of the potential for the VenoValve spreads among vascular surgeons whose practices include the treatment of venous diseases," said Robert Berman, enVVeno Medical's Chief Executive Officer. "The VenoValve has the potential to be the first FDA approved treatment for deep venous CVI, and we are attempting to reach the top of a mountain that nobody has successfully climbed and with many failed attempts over the past several decades. With the summit of the mountain finally in sight, this is an exciting time for our company and for the millions of patients with severe deep venous CVI who have no effective treatment options."
Severe, deep venous CVI is a debilitating disease that is most often caused by blood clots (deep vein thromboses or DVTs) in the deep veins of the leg. When valves inside of the veins of the leg fail, blood flows in the wrong direction and pools in the lower leg, causing pressure within the veins of the leg to increase (venous hypertension). Symptoms of severe CVI include leg swelling, pain, edema, and in the most severe cases, recurrent open sores known as venous ulcers. The disease can severely impact everyday functions such as sleeping, bathing, dressing, and walking, and is known to result in high rates of depression and anxiety. There are currently no effective treatments for severe CVI of the deep vein system caused by valvular incompetence. Estimates indicate that CVI costs the U.S. healthcare system in excess of $4 billion each year.
The Venous Insufficiency Epidemiological and Economic Study Quality of Life/Symptoms (VEINES-QoL/Sym) questionnaire is a validated, disease-specific instrument to measure patient-reported quality of life and symptom severity in individuals with chronic venous disease. By assessing factors such as pain, functional limitations, and psychosocial impacts, VEINES-QoL/Sym provides a standardized framework for evaluating treatment outcomes and guiding clinical decision-making.
About enVVeno Medical Corporation
enVVeno Medical (NASDAQ:NVNO) is an Irvine, California-based, late clinical-stage medical device Company focused on the advancement of innovative bioprosthetic (tissue-based) solutions to improve the standard of care for the treatment of venous disease. The Company's lead product, the VenoValve®, is a first-in-class surgical replacement venous valve being developed for the treatment of deep venous Chronic Venous Insufficiency (CVI). The Company is also developing a non-surgical, transcatheter based replacement venous valve for the treatment of deep venous CVI called enVVe®. CVI occurs when valves inside of the veins of the leg become damaged, resulting in the backwards flow of blood (reflux), blood pooling in the lower leg, increased pressure in the veins of the leg (venous hypertension) and in severe cases, venous ulcers that are difficult to heal and become chronic. Both the VenoValve and enVVe are designed to act as one-way valves, to help assist in propelling blood up the leg, and back to the heart and lungs. The VenoValve is currently being evaluated in the SAVVE U.S. pivotal study and the Company is currently performing the final testing necessary to seek approval for the pivotal trial for enVVe.
Cautionary Note on Forward-Looking Statements
This press release and any statements of stockholders, directors, employees, representatives and partners of enVVeno Medical Corporation (the "Company") related thereto contain, or may contain, among other things, certain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements involve significant risks and uncertainties. Such statements may include, without limitation, statements identified by words such as "projects," "may," "will," "could," "would," "should," "believes," "expects," "anticipates," "estimates," "intends," "plans," "potential" or similar expressions. These statements are based upon the current beliefs and expectations of the Company's management and are subject to significant risks and uncertainties, including those detailed in the Company's filings with the Securities and Exchange Commission. Actual results and timing (may differ significantly from those set forth or implied in the forward-looking statements. Forward-looking statements involve certain risks and uncertainties that are subject to change based on various factors (many of which are beyond the Company's control). The Company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future presentations or otherwise, except as required by applicable law.
###
INVESTOR CONTACT:
Jenene Thomas, JTC Team, LLC
[email protected]
(908) 824-0775
SOURCE: enVVeno Medical Corporation
View the original press release on ACCESS Newswire
Ch.P.Lewis--AT