logo
Audifort Update Reveals Breakthrough Botanical Formulation for Hearing Health Support in 2025

Audifort Update Reveals Breakthrough Botanical Formulation for Hearing Health Support in 2025

Business Upturn26-06-2025
New York, June 25, 2025 (GLOBE NEWSWIRE) —
In a notable update from the natural health community, Audifort has announced the latest iteration of its research-driven formula. Built on principles of botanical synergy and holistic hearing support, Audifort introduces a reimagined approach to auditory wellness.
In This Release, You'll Learn: What Audifort is and how its formulation aligns with hearing health goals
The natural ingredients backed by scientific inquiry
Why auditory support is gaining attention in 2025
Key insights into emerging research on inner ear health
Educational context around supporting hearing naturally
How users are approaching lifestyle-based hearing wellness
Answers to frequently asked questions from new users
Botanical Formulation Centered Around Holistic Support
Audifort is positioned at the intersection of herbal science and functional health strategies, focusing on nurturing auditory function through a carefully selected blend of plant-based ingredients. Rather than framing itself as a treatment or cure, Audifort is designed as a support mechanism rooted in nutritional science.
The blend includes over 20 plant-based ingredients, each selected for its role in maintaining healthy auditory processes. Some of the primary ingredients featured include: Grape Seed Extract : Known for its antioxidant activity, contributing to the protection of delicate cells involved in hearing.
: Known for its antioxidant activity, contributing to the protection of delicate cells involved in hearing. Green Tea : Commonly referenced for circulatory support, potentially aiding in improved blood flow to inner ear structures.
: Commonly referenced for circulatory support, potentially aiding in improved blood flow to inner ear structures. Capsicum Annuum : Recognized for its role in supporting a healthy inflammatory response, essential to the inner ear environment.
: Recognized for its role in supporting a healthy inflammatory response, essential to the inner ear environment. Gymnema Sylvestre : Traditionally used in wellness formulas and included for its potential synergy with other botanicals.
: Traditionally used in wellness formulas and included for its potential synergy with other botanicals. Maca Root and GABA: Included for their adaptogenic and neurological support roles.
This multifaceted ingredient profile aims to provide support for individuals seeking non-invasive, dietary-based strategies to bolster hearing function.
A Broad Appeal Across Demographics
Audifort has been used by men and women across a wide range of age groups—from individuals in their 30s to those in their 70s. Its development is grounded in modern scientific perspectives, yet the formula remains gentle and plant-based. It is assembled in the United States and follows quality control measures aimed at maintaining ingredient integrity.
Whether you're noticing the signs of hearing fatigue or simply looking for a more natural addition to your wellness routine, Audifort's thoughtful blend makes it a versatile companion to daily health habits.
What Users Have Reported
Some people say the first thing they noticed was a shift in clarity—an easier time picking up conversations, or less buzzing in quiet moments. Others mention a gentle uptick in energy and mental sharpness. These stories aren't unusual, especially for those who've taken the formula consistently over several weeks.
That said, results can vary. The team behind Audifort emphasizes that benefits are gradual, building with time as the body incorporates the nutrients. Most consistent outcomes tend to emerge after three to four months of daily use, aligning with the broader science around plant-based nutritional support.
Exploring Daily Lifestyle Synergies
Many users who integrate Audifort into their wellness routines also explore parallel habits to promote overall cognitive clarity and auditory balance. These may include mindfulness practices, dietary awareness, better sleep routines, and reduced exposure to environmental noise.
Educational materials bundled with Audifort often emphasize these holistic practices—not as a substitute for professional medical advice, but as part of a more intentional lifestyle. The goal is to help individuals become more conscious of their auditory environment and the small choices that influence sensory resilience over time.
The value of such choices lies in consistency. Something as simple as reducing headphone volume or taking mindful breaks from noise pollution can work in tandem with nutritional support to foster a more protective daily rhythm.
Nutritional Support and the Modern Wellness Landscape
In an era where digital connectivity has dramatically increased the average person's exposure to sound, the need for proactive auditory support has never been more relevant. Urban environments, earbuds, and device alerts all contribute to constant stimulation that can, over time, take a toll on the auditory system.
This shift has sparked growing interest in nutritional strategies that can complement conventional self-care routines. Products like Audifort reflect a broader movement toward plant-based, integrative approaches to wellness—ones that prioritize prevention, self-education, and consistent daily practices.
While medical technology has made major advances in hearing devices, many individuals are looking to support their health naturally before problems progress to the point of intervention. For these consumers, formulas like Audifort serve as one tool among many in crafting a more intentional lifestyle.
Best Practices for Incorporation
Audifort is taken twice a day: once in the morning before breakfast, and again before lunch. You can use a full dropper directly under your tongue or dissolve it in a glass of water or juice. It's a flexible process—simple enough to become part of your routine without disruption.
Every dropper delivers a measured amount of the formula, and according to guidance on the official site, regular use is key to experiencing its full potential.
Transparent Policies and Fulfillment
Audifort is offered exclusively through its official website to ensure quality and authenticity. Orders typically ship within 24 business hours via premium carriers, and most domestic deliveries arrive in 5 to 10 business days. Users receive email tracking to follow each step of the shipment.
Payment is processed securely through encrypted SSL technology, and there are no subscriptions or surprise charges—just a one-time payment and clear fulfillment.
Navigating the Fine Print: A Human-Centered Approach
Navigating terms and conditions doesn't have to feel like reading a legal document. At its core, the Audifort site exists to provide educational information and a platform for responsible wellness choices. It's designed for adults, age 18 and older, who understand that supplements are not substitutes for medical care.
The creators emphasize that Audifort is not intended to treat, cure, or diagnose any disease. It is best understood as part of a holistic lifestyle—something to be discussed with your doctor, especially if you're taking medication, managing allergies, or exploring other health changes.
Your experience with any nutritional formula is deeply personal. Factors such as consistency, individual health background, and lifestyle habits all play a role. The team encourages users to reach out with questions and stay engaged with any health decisions they make.
Frequently Asked Questions (FAQs)
Q: Who can take Audifort?
A: Adults aged 18 and older who are interested in nutritional hearing support. Not suitable for children or those managing serious health conditions without physician oversight.
Q: When will I start noticing changes?
A: Many users start to notice subtle shifts in clarity or energy within a week. Deeper results often appear over three to four months of consistent use.
Q: How should Audifort be taken?
A: One dropper in the morning before breakfast, another before lunch. Place under your tongue or mix with water or juice.
Q: What if I have food sensitivities or allergies?
A: Review the label and speak with your healthcare provider to confirm suitability.
Q: Can I take Audifort while on medication?
A: Always consult your physician before beginning any new nutritional supplement while taking medication.
Q: Is the website secure for purchase?
A: Yes. Transactions use encrypted SSL protocols, and purchases are one-time only with no recurring charges.
Q: What is the refund policy?
A: There's a 90-day return policy for customers who would like to explore the formula risk-free. Details are available on the official returns page.
Growing Interest in Hearing Wellness
As public awareness of age-related hearing challenges increases, many are turning to lifestyle-based approaches to maintain cognitive and sensory performance. Audifort's positioning aligns with this trend, focusing on preventative support rather than reactive treatment.
Recent studies, including those published by the National Institute on Deafness and Other Communication Disorders (NIDCD) and Georgetown University Medical Center, have shed light on the connection between neuroplasticity and auditory function. These insights contribute to a broader understanding of how brain regions interact with hearing pathways and how certain nutrients and antioxidants may play a supportive role.
Distinct From Conventional Hearing Aids or Medical Interventions
Audifort is not a device, treatment, or substitute for clinical care. It does not replace hearing aids, medical diagnostics, or prescriptions. Instead, it serves as an integrative tool for individuals focused on nutritional wellness. The formula's design is consistent with ongoing exploration into dietary supplementation and wellness practices.
Educational content provided alongside the formulation includes resources like: The Deep Sleep Activation Protocol
The Brainwire Regeneration Blueprint
These materials focus on lifestyle and sleep support as part of a comprehensive approach to well-being.
A Natural Strategy, Not a Substitute for Medical Advice
While botanical ingredients have long been explored for their antioxidant and adaptogenic properties, users are advised to consult with a healthcare provider before initiating any nutritional regimen. Audifort is intended for adult consumers as part of a balanced lifestyle.
Supporting Materials and Reference Studies
Audifort's ingredient selection draws from published literature and ongoing inquiry into nutritional neurobiology. Scientific references associated with relevant areas of study include: Kennedy, D.O. (2016). B Vitamins and the Brain: Mechanisms, Dose and Efficacy.
White et al. (2006). Mammalian Cochlear Supporting Cells Can Divide and Transdifferentiate into Hair Cells. Nature.
Nature. Schlee, W. et al. (2009). Mapping Cortical Hubs in Tinnitus.
Kumar, G.P. & Khanum, F. Neuroprotective Potential of Phytochemicals.
Additional research from NIDCD, Georgetown University Medical Center, and related institutions
These citations provide academic context for the formulation, although no direct therapeutic claims are made.
Pricing, Fulfillment, and Disclosures
Audifort is made available by BuyGoods, a Delaware-based retailer, and is currently offered with bundled educational resources for consumers. Delivery logistics and fulfillment services are handled directly by the distributor.
Disclaimer: Statements regarding Audifort have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease. Individuals with a known medical condition should consult a licensed physician prior to use. No results are guaranteed, and individual outcomes may vary.
Affiliate Disclosure: Some references or links associated with Audifort may generate commissions to the publisher. This disclosure ensures transparency in compliance with applicable advertising regulations.
Contact: Company: Audifort
Audifort Customer Support: [email protected]
[email protected] Phone: +1-866-374-5018 (Mon – Sun, 10 AM – 1 AM EST)
+1-866-374-5018 (Mon – Sun, 10 AM – 1 AM EST) Returns Address: 19655 E 35th Dr #100, Aurora, CO 80011, USA
19655 E 35th Dr #100, Aurora, CO 80011, USA Official Website: www.audifort.com/
Disclaimer: The above press release comes to you under an arrangement with GlobeNewswire. Business Upturn takes no editorial responsibility for the same.
Ahmedabad Plane Crash
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Onco360 adds Modeyso™ (dordaviprone) to portfolio of Oncology and Rare Cancer therapies as a National Specialty Pharmacy Provider
Onco360 adds Modeyso™ (dordaviprone) to portfolio of Oncology and Rare Cancer therapies as a National Specialty Pharmacy Provider

Yahoo

time2 hours ago

  • Yahoo

Onco360 adds Modeyso™ (dordaviprone) to portfolio of Oncology and Rare Cancer therapies as a National Specialty Pharmacy Provider

LOUISVILLE, Ky., Aug. 13, 2025 (GLOBE NEWSWIRE) -- Onco360®, the nation's leading independent Specialty Pharmacy, has been selected as a pharmacy partner by Jazz Pharmaceuticals for Modeyso™ (dordaviprone). It is indicated for the treatment of adult and pediatric patients one year of age and older with diffuse midline glioma harboring an H3 K27M-mutation with progressive disease following prior therapy.1 This indication was approved based on five open-label, non-randomized clinical trials conducted in the U.S. (ONC006 [NCT02525692], ONC013 [NCT03295396], ONC014 [NCT03416530], ONC016 [NCT05392374], and ONC018 [NCT03134131]).1 'Onco360 is grateful for the opportunity to add Modeyso™ to our expansive portfolio of cancer and rare disease therapies as the first and only FDA-approved treatment for pediatric and adult patients with diffuse midline glioma,' said Benito Fernandez. 'We are proud and humbled to be part of this innovative treatment in support of patients, caregivers and families impacted by this devastating disease.' Dordaviprone is a protease activator of the mitochondrial caseinolytic protease P (ClpP) and inhibits dopamine D2 receptor (DRD2). In vitro, dordaviprone activates the integrated stress response, induces apoptosis, and alters mitochondrial metabolism, leading to restored histone H3 K27 trimethylation in H3 K27M-mutant diffuse glioma.1 The efficacy of Modeyso was evaluated in an integrated efficacy population of 50 adult and pediatric patients with recurrent H3 K27M-mutant diffuse midline glioma enrolled across five open-label, non-randomized clinical trials.1 The primary outcome was overall response rate (ORR) of 22% (95% CI: 12,36). The trial also demonstrated a duration of response of 10.3 months (95% CI: 7.3, 15.2) with 73% maintaining their response for at least six months and 27% for at least 12 months.1 Dordaviprone demonstrated manageable safety and tolerability adverse events. The most common adverse reactions (≥20 %; all causality) experienced with dordaviprone were fatigue, headache, nausea, vomiting, and musculoskeletal pain.1 Please see the full Prescribing Information for Modeyso. About Onco360 Oncology Pharmacy:Onco360 is the nation's largest independent Oncology Pharmacy and clinical support services company. Onco360 was founded in 2003 to bring together the stakeholders involved in the cancer treatment process and serve the specialized needs of oncologists, patients, hospitals, cancer centers of excellence, manufacturers, health plans, and payers. It dispenses nationally through its network of URAC-, and ACHC-accredited Oncology Pharmacies. Onco360 is headquartered in Louisville, Kentucky, and is a flagship specialty pharmacy brand of PharMerica Corporation, a leading institutional pharmacy, specialty infusion, and hospital services company servicing healthcare facilities in the United States. For more information about Onco360, please visit Media Contact: Benito Fernandez, Chief Commercial References:1Modeyso™ (Dordaviprone) [Package Insert]. Palo Alto, CA. Jazz Pharmaceuticals. in to access your portfolio

Iterum Therapeutics launches ORLYNVAH™, the first and only oral penem antibiotic in the U.S.
Iterum Therapeutics launches ORLYNVAH™, the first and only oral penem antibiotic in the U.S.

Yahoo

time3 hours ago

  • Yahoo

Iterum Therapeutics launches ORLYNVAH™, the first and only oral penem antibiotic in the U.S.

FDA-approved antibiotic with the power of a penem in a novel oral formulation, offering a vital alternative in treating uncomplicated urinary tract infections DUBLIN and CHICAGO, Aug. 20, 2025 (GLOBE NEWSWIRE) -- Iterum Therapeutics plc (Nasdaq: ITRM), a company focused on delivering next generation oral and IV antibiotics to treat infections caused by multi-drug resistant pathogens in both community and hospital settings, today announced the U.S. commercial launch of ORLYNVAH™ (sulopenem etzadroxil and probenecid) oral tablets. The Food and Drug Administration (FDA) approved ORLYNVAH™ for adult women with uncomplicated urinary tract infections (uUTIs) caused by Escherichia coli, Klebsiella pneumoniae or Proteus mirabilis with limited or no alternative oral antibacterial options in October 2024. ORLYNVAH™ is the first oral penem antibiotic commercially available in the U.S. and the first new branded product to be introduced in the U.S. for uUTI in more than 25 years – offering a critical option for patients and physicians facing a shrinking arsenal of effective oral therapies. Sixty percent of women experience a urinary tract infection in their lifetime and 44% experience three or more episodes annually. It is the most common outpatient infection in women in the United States, and resistance continues to increase. According to a 2024 U.S. study in approximately 150,000 patients with uncomplicated UTIs: 57% of initial infections were resistant to at least one antibiotic class; and 13% were resistant to three or more. Without new, safe and effective oral therapies, resistant uUTIs are expected to inflate healthcare costs and may lead to poor patient outcomes in the U.S., including the need for additional courses of therapy, emergency room visits or hospitalizations, all of which underscore the urgent need for innovation in this space. 'The availability of ORLYNVAH™ is tremendous news for clinicians and patients alike,' said Marjorie Golden, MD, FIDSA, Site Chief, Infectious Disease, St. Raphael Campus Yale New Haven Hospital. 'The launch of ORLYNVAH™ provides a new treatment option with impressive efficacy data to treat appropriate adult women suffering from difficult-to-treat uUTIs.' Dr. Golden added, 'For patients who currently have limited treatment options, ORLYNVAH™ provides a long overdue oral alternative that allows for treatment in the community. This paradigm shift in the management of patients with uUTI will not only reduce emergency department visits and hospital admissions, but it will also favorably impact patients' quality of life.' 'Our mission is to create new antibiotics for patients and to be a treatment alternative to address substantial unmet medical needs in the community,' said Corey Fishman, Chief Executive Officer of Iterum Therapeutics. 'For many people with multidrug-resistant uUTIs, options have been exhausted. We're proud to introduce ORLYNVAH™—the first oral penem ever approved by the FDA—giving clinicians and patients a much-needed new therapy.' To support patient access, Iterum Therapeutics is launching a copay savings program allowing eligible patients to obtain ORLYNVAH™ for as little as $25. For more information about ORLYNVAH™, including full prescribing information, please visit Uncomplicated urinary tract infections (uUTIs) are a common bladder infection typically confined to the lower urinary tract in otherwise healthy women with no structural abnormalities of the urinary tract—caused by Escherichia coli, Klebsiella pneumoniae or Proteus mirabilis. About Iterum Therapeutics plcIterum Therapeutics plc is focused on delivering differentiated anti-infectives aimed at combatting the global crisis of multi-drug-resistant pathogens to significantly improve the lives of people affected by serious and life-threatening diseases around the world. Iterum is advancing the development of its first compound, sulopenem, a novel penem anti-infective compound, with an oral formulation and IV formulation. Sulopenem has demonstrated potent in vitro activity against a wide variety of gram-negative, gram-positive and anaerobic bacteria resistant to other antibiotics. Iterum has received U.S. Food and Drug Administration approval for ORLYNVAH™ (oral sulopenem) for the treatment of uncomplicated urinary tract infections (uUTIs) caused by Escherichia coli, Klebsiella pneumoniae or Proteus mirabilis in adult women with limited or no alternative oral antibacterial treatment options, and ORLYNVAH™ is commercially available in the United States. Iterum has also been granted Qualified Infectious Disease Product (QIDP) and Fast Track designations for its oral and IV formulations of sulopenem in seven indications. For more information, please visit About ORLYNVAH™ORLYNVAH™ is a novel oral penem antibiotic for the treatment of uUTIs. ORLYNVAH™ possesses potent activity against species of Enterobacterales including those that encode ESBL or AmpC-type ß-lactamases that confer resistance to third generation cephalosporins. Cautionary Note Regarding Forward-looking StatementsThis press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. These forward-looking statements include, without limitation, statements regarding Iterum's plans, strategies and prospects for its business, including the development, therapeutic and market potential of ORLYNVAH™ and the success of Iterum's commercialization of ORLYNVAH™ in the U.S. In some cases, forward-looking statements can be identified by words such as 'may,' 'believes,' 'intends,' 'seeks,' 'anticipates,' 'plans,' 'estimates,' 'expects,' 'should,' 'assumes,' 'continues,' 'could,' 'would,' 'will,' 'future,' 'potential' or the negative of these or similar terms and phrases. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause Iterum's actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Forward-looking statements include all matters that are not historical facts. Actual future results may be materially different from what is expected due to factors largely outside Iterum's control, including Iterum's successful commercialization of ORLYNVAH™ in the U.S. with its commercial partner, EVERSANA, including Iterum's ability to maintain and continue to build a sales force for the commercialization of ORLYNVAH™ in the U.S., the ability of shareholders and other stakeholders to realize any value or recovery as part of a wind down process if the commercialization of ORLYNVAH™ in the U.S. is unsuccessful, the market opportunity for and the potential market acceptance of ORLYNVAH™ for uUTIs caused by certain designated microorganisms in adult women who have limited or no alternative oral antibacterial treatment options, the potential impact of resistant uUTIs on healthcare costs and medical outcomes for uUTI patients in the U.S., Iterum's ability to continue as a going concern, uncertainties inherent in the conduct of clinical and non-clinical development, changes in regulatory requirements or decisions of regulatory authorities, the timing or likelihood of regulatory filings and approvals, changes in public policy or legislation, the actions of third-party clinical research organizations, suppliers and manufacturers, the accuracy of Iterum's expectations regarding how far into the future Iterum's cash on hand will fund Iterum's ongoing operations, Iterum's ability to maintain its listing on the Nasdaq Capital Market and other factors discussed under the caption 'Risk Factors' in its Quarterly Report on Form 10-Q filed with the SEC on August 5, 2025, and other documents filed with the SEC from time to time. Forward-looking statements represent Iterum's beliefs and assumptions only as of the date of this press release. Except as required by law, Iterum assumes no obligation to update these forward-looking statements publicly, or to update the reasons actual results could differ materially from those anticipated in the forward-looking statements, even if new information becomes available in the future. PRESS CONTACTJennifer PerciballiOak+Cannon PR for Iterumjennifer@ Investor RelationsJudy MatthewsChief Financial Officer Iterum Therapeutics 312-778-6073IR@

The Wistar Institute Receives $17 Million NIH Grant for Personalized HIV Cure Research
The Wistar Institute Receives $17 Million NIH Grant for Personalized HIV Cure Research

Yahoo

time20 hours ago

  • Yahoo

The Wistar Institute Receives $17 Million NIH Grant for Personalized HIV Cure Research

Philadelphia-led consortium is selected to tailor HIV curative strategies to participant Philadelphia, PA, Aug. 19, 2025 (GLOBE NEWSWIRE) -- The Wistar Institute announces the National Institutes of Health (NIH) granted a five-year, $17 million research award to launch iCure Consortium to develop individualized 'cure regimens' for HIV. The Wistar-led, iCure Consortium's objective is to advance strategies to cure HIV through tailored personalized medicine. 'Today 38 million people still live with HIV worldwide, and 1.3 million contract the virus each year,' said Luis J. Montaner, D.V.M., iCure principal investigator, executive vice president of The Wistar Institute and director of Wistar's HIV Cure and Viral Diseases Center. 'For the first time, this grant brings our best team together working towards a cure tailored to each participant by pairing the latest in neutralizing antibody and cell-therapy breakthroughs against the unique, person-specific features of HIV.' iCure Consortium will test a six-part, individually-tailored therapy designed to wipe out the persistent viral reservoir that remains after antiretroviral therapy in an effort to deliver durable, drug-free remission. The project combines six advanced tactics—neutralizing antibodies, mRNA therapy, viral binders, engineered CAR-T and 'Natural Killer' (NK) cells, and precision latency 'wake-up' drugs—all designed against each patient's unique virus. 'Ending HIV demands more than management—it demands eradication,' said Drew Weissman, M.D., Ph.D., iCure co‑principal investigator, 2023 Nobel Laureate and Roberts Family Professor in Vaccine Research at the Perelman School of Medicine at the University of Pennsylvania. 'This project now allows us to apply our breakthroughs in RNA therapy as part of a cure-directed strategy.' How iCure Works• Wake the latent virus• Map and target unique weak spots with tailored antibodies• Destroy infected cells using 'super‑charged' CAR‑T and NK cells• Enhance clearance and block relapse with bispecific binders In the first step, researchers reactivate the virus in a sample of the participant's blood and identify mutations that the participant has not yet developed antibodies against. They then develop a tailored antibody therapy cocktail specifically designed against these specific mutations. In the next stage, researchers focus on preventing HIV from returning. To do this, they develop person-specific antibodies or small molecule binders that can act as 'homing devices' — beacons that can lead immune cells to the latent virus. Then they genetically modify CAR-T cells and NK cells (immune cells that destroy viruses) to express or use these homing devices to better clear infected cells. Finally, researchers further enhance NK cells. First, they develop stronger and more durable cells, called adaptive NK cells, by supercharging their virus-killing ability. Then, they deploy small-molecule drugs called bispecifics, which bind NK cells to the infected cells they are targeting. "iCure takes full advantage of the advances made in understanding how and where HIV hides from the immune system," said Montaner. "We've built on our knowledge and can use that information to identify a first of its kind targeting to a person's unique HIV features." iCure furthers the research groundwork laid by the BEAT-HIV Martin Delaney Collaboratory ( a Philadelphia-based consortium of more than 95 leading HIV researchers co-led by Dr. Montaner. Montaner called the NIH grant a 'once in a lifetime opportunity' that reflects Wistar's track record as a scientific leader in the effort to develop an HIV cure, as well as its grassroots support and collaboration with the HIV community. 'By the end of this study we hope to have a process by which to identify the virus that we need to go after in each person and have a basis to design clinical trials choosing the best of these strategies to move forward,' said Montaner. Other institutions participating in this study include Johns Hopkins Medicine and iCure co-principal investigator Robert Siliciano, M.D., Ph.D., the University of Pennsylvania, Philadelphia FIGHT, the Ragon Institute at Harvard University, George Washington University, Duke University, and Massachusetts Institute of Technology. The iCure program is funded by the National Institute of Allergy and Infectious Diseases, part of NIH, under award number UM1AI191272. ### The Wistar Institute is an international leader in biomedical research with special expertise in cancer research and vaccine development. Founded in 1892 as the first independent nonprofit biomedical research institute in the United States, Wistar has held the prestigious Cancer Center designation from the National Cancer Institute since 1972. The Institute works actively to ensure that research advances move from the laboratory to the clinic as quickly as possible. CONTACT: Darien Sutton The Wistar Institute 215-870-2048 dsutton@ in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store