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Watchdog bans host of ads for prescription-only weight-loss medications

Watchdog bans host of ads for prescription-only weight-loss medications

Yahooa day ago
A watchdog has cracked down on a host of weight-loss jab providers for advertising the prescription-only medications to the public.
The Advertising Standards Authority (ASA) said the nine rulings against the ads – one featuring reality TV personality Gemma Collins – made it 'crystal clear' that all injectable forms of weight-loss medication were prescription-only and therefore could not advertised to the public.
In December, the ASA warned businesses and individuals who were targeting members of the public with ads for the medicines.
It said no-one operating in the industry could say they had not been warned that weight-loss prescription-only medicines 'must not be promoted to the public'.
The ads banned this week include an Instagram post by Collins, posted on January 6, which promoted the weight-loss service Yazen.
In a video, Collins stated: 'I'm starting this year two sizes down, thanks to Yazen's weight loss app and medication. It's really quick and easy to get started with Yazen, it has absolutely changed my life… I finally found something that actually I lose weight on.'
She continued: 'Yes, there's, you know, reports and stuff. And I'm not telling anyone to go on this medication, but it is prescribed on the NHS.'
Two complainants challenged whether the ad breached rules because it promoted prescription-only medication to the public.
Yazen said the post had been intended to share information about their 'holistic, responsible approach to weight loss', and had not been intended to focus solely on medication.
Following notification of the complaint, and in agreement with Collins, the post has been amended to remove any reference to prescription-only medications.
Yazen said they would ensure that future posts were compliant with the advertising code.
Collins said she took her responsibilities under the advertising code seriously and strove to comply with them.
She accepted that her posts had promoted the Yazen weight-loss service and app, and said Yazen would approve any marketing materials she might post in future, and she would follow any guidance that the ASA provided.
The ASA also banned an ad for prescription-only weight-loss medication posted by CheqUp, which read: 'No GP or pharmacy visit, just a 2 minute online consultation.'
CheqUp told the ASA that they believed the ad had been created in line with what had become widespread industry practice in the weight-loss sector.
They assured the ASA that the ad would not appear again.
Other providers who have had their ads banned include pharmacyonline.co.uk, HealthExpress.co.uk, Juniper UK, Cloud Pharmacy, and Phlo Clinic and SemaPen.
The ASA said the rulings established the advertising of named weight-loss drugs such as Wegovy, Mounjaro, Ozempic and Saxenda was banned, as was the use of various claims such as 'obesity treatment jab' and 'weight loss pen'.
In April, the ASA said a search in January found around 1,800 unique paid-for weight-loss ads which were identified as potentially advertising a prescription-only medicine.
It has published a joint Enforcement Notice with the Medicines and Healthcare products Regulatory Agency and General Pharmaceutical Council, making clear that ads for named weight-loss prescription-only medications are prohibited, including online, on social media and by influencers.
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Inventiva names Jason Campagna as President of R&D and Chief Medical Officer and Martine Zimmermann as Executive Vice President of Regulatory Affairs and Quality Assurance
Inventiva names Jason Campagna as President of R&D and Chief Medical Officer and Martine Zimmermann as Executive Vice President of Regulatory Affairs and Quality Assurance

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Inventiva names Jason Campagna as President of R&D and Chief Medical Officer and Martine Zimmermann as Executive Vice President of Regulatory Affairs and Quality Assurance

Jason Campagna, MD, PhD, joins Inventiva as President of R&D and Chief Medical Officer, succeeding Pierre Broqua, PhD, and Michael Cooreman, MD Martine Zimmermann, PharmD, joins as Executive Vice President of Regulatory Affairs and Quality Assurance These key leadership appointments underscore Inventiva's commitment to long-term growth and operational excellence, with topline results from NATiV3 on track for the second half of 2026 Daix (France), New York City (New York, United States), July 9, 2025 – Inventiva (Euronext Paris and Nasdaq: IVA) ('Inventiva' or the 'Company'), a clinical-stage biopharmaceutical company focused on the development of oral therapies for the treatment of metabolic dysfunction-associated steatohepatitis ('MASH'), today announced a leadership transition with the appointment of Jason Campagna, MD, PhD, as President of Research and Development ('R&D') and Chief Medical Officer ('CMO') and Martine Zimmermann, PharmD, as Executive Vice President ('EVP') of Regulatory Affairs and Quality Assurance. Dr. Campagna is joining Inventiva's executive leadership team and brings extensive expertise in the MASH field. He succeeds Pierre Broqua, PhD, co-founder and Chief Scientific Officer, who is transitioning to a consulting role as Scientific Advisor, and Michael Cooreman, MD, departing as CMO of the Company. Dr. Campagna most recently was the CMO at Q32 Bio and prior to that was the MASH Global Program Lead and CMO at Intercept Pharmaceuticals. Dr. Zimmermann is also joining the Company's executive leadership team. She was most recently Senior Vice President, Head of Regulatory Affairs at Ipsen where she successfully led a team that secured regulatory approvals of two liver disease drugs, including Iqirvo®, a dual PPARα/δ agonist, for the treatment of primary biliary cholangitis. Prior to Ipsen, Dr. Zimmermann was Senior Vice President and Head of Global Regulatory Affairs & Quality at Alexion Pharma (also known as AstraZeneca Rare Disease). Frederic Cren, CEO of Inventiva stated: 'Jason and Martine both bring exceptional leadership and experience during this pivotal time for the Company as we plan for the readout of our NATiV3 Phase 3 study next year and lanifibranor's potential regulatory approval and commercialization. Having played an integral part in the creation and building of Inventiva, Pierre will continue to actively support the team in a scientific consulting role. I would also like to express my gratitude to Michael for his scientific leadership and contributions in advancing lanifibranor to this stage and we wish him every success in his future endeavors.' Jason Campagna, MD, PhD, President, R&D and CMO of Inventiva commented: 'Inventiva has built a robust scientific and clinical foundation, and I'm thrilled to join the team at this pivotal moment as we advance lanifibranor toward anticipated regulatory submissions. Having led the design and execution of one of the field's most advanced clinical programs at Intercept—including the first-ever NDA submission in this indication—I've seen firsthand both the scientific complexity and the urgency of bringing effective therapies to patients with MASH. I believe the promising results of the Phase 2b NATIVE trial reflect the thoughtful design of lanifibranor development program—and that's deeply exciting to me. With lanifibranor well on its way in the Phase 3 NATiV3 registrational trial, I look forward to working closely with the exceptional team at Inventiva to deliver on the promise of bringing a novel treatment to patients with MASH.' Martine Zimmermann, PharmD, Executive Vice President of Regulatory Affairs and Quality Assurance of Inventiva said: "I'm excited to take on this leadership role at a time when Inventiva is entering a critical regulatory phase for lanifibranor, a first-in-class pan-PPAR agonist for the treatment of MASH. In my career, I've been closely involved in leading global regulatory strategy and approval of compounds for the treatment of chronic liver diseases, including a PPAR, in a number of geographies, including the US, Europe and Japan. I am now eager to apply that experience to support lanifibranor toward a potential approval." About Inventiva Inventiva is a clinical-stage biopharmaceutical company focused on the research and development of oral small molecule therapies for the treatment of patients with MASH and other diseases with significant unmet medical need. The Company is currently evaluating lanifibranor, a novel pan-PPAR agonist, in the NATiV3 pivotal Phase 3 clinical trial for the treatment of adult patients with MASH, a common and progressive chronic liver disease. Inventiva is a public company listed on compartment B of the regulated market of Euronext Paris (ticker: IVA, ISIN: FR0013233012) and on the Nasdaq Global Market in the United States (ticker: IVA). Contacts InventivaPascaline ClercEVP, Strategy and Corporate Affairsmedia@ 202 499 8937 ICR HealthcareMedia relations Alexis Feinberg inventivapr@ +1 203 939 2225 ICR HealthcarePatricia L. BankInvestor relations +1 415 513 1284 Important Notice This press release contains certain 'forward-looking statements' within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, included in this press release are forward-looking statements. These statements include, but are not limited to, Inventiva's clinical trials, including Inventiva's ongoing NATiV3 Phase 3 clinical trial of lanifibranor in MASH, including related timing and regulatory matters with respect thereto, clinical trial data releases and publications, the information, insights and impacts that may be gathered from clinical trials, the potential therapeutic benefits of Inventiva's product candidates, potential regulatory submissions, approvals and commercialization, the effective start date of Dr. Campagna and Mrs. Zimmerman, the clinical development of and regulatory plans and pathway for lanifibranor, and future activities, expectations, plans, growth and prospects of Inventiva. Certain of these statements, forecasts and estimates can be recognized by the use of words such as, without limitation, 'believes', 'anticipates', 'expects', 'intends', 'plans', 'seeks', 'estimates', 'may', 'will', 'would', 'could', 'might', 'should', 'designed', 'hopefully', 'target', 'potential', 'possible', 'aim', and 'continue' and similar expressions. Such statements are not historical facts but rather are statements of future expectations and other forward-looking statements that are based on management's beliefs. These statements reflect such views and assumptions prevailing as of the date of the statements and involve known and unknown risks and uncertainties that could cause future results, performance, or future events to differ materially from those expressed or implied in such statements. Actual events are difficult to predict and may depend upon factors that are beyond Inventiva's control. There can be no guarantees with respect to product candidates that the clinical trial results will be available on their anticipated timeline, that future clinical trials will be initiated as anticipated, that product candidates will receive the necessary regulatory approvals, or that any of the anticipated milestones by Inventiva or its partners will be reached on their expected timeline, or at all. Future results may turn out to be materially different from the anticipated future results, performance or achievements expressed or implied by such statements, forecasts and estimates due to a number of factors, including that interim data or data from any interim analysis of ongoing clinical trials may not be predictive of future trial results, the recommendation of the DMC may not be indicative of a potential marketing approval, Inventiva cannot provide assurance on the impacts of the Suspected Unexpected Serious Adverse Reaction on the results or timing of the NATiV3 trial or regulatory matters with respect thereto, that Inventiva is a clinical-stage company with no approved products and no historical product revenues, Inventiva has incurred significant losses since inception, Inventiva has never generated any revenue from product sales, Inventiva will require additional capital to finance its operations, in the absence of which, Inventiva may be required to significantly curtail, delay or discontinue one or more of its research or development programs or be unable to expand its operations or otherwise capitalize on its business opportunities and may be unable to continue as a going concern, Inventiva's ability to obtain financing, to enter into potential transactions, Inventiva's future success is dependent on the successful clinical development, regulatory approval and subsequent commercialization of lanifibranor, preclinical studies or earlier clinical trials are not necessarily predictive of future results and the results of Inventiva's and its partners' clinical trials may not support Inventiva's and its partners' product candidate claims, Inventiva's expectations with respect to its clinical trials may prove to be wrong and regulatory authorities may require additional holds and/or amendments to Inventiva's clinical trials, Inventiva's expectations with respect to the clinical development plan for lanifibranor for the treatment of MASH may not be realized and may not support the approval of a New Drug Application, Inventiva's ability to identify additional products or product candidates with significant commercial potential, Inventiva's expectations with respect to its pipeline prioritization plan and related workforce reduction, including whether the plan will be implemented and the timing, potential benefits, expenses and consequences relating thereto, Inventiva's ability to execute on its commercialization, marketing and manufacturing capabilities and strategy, Inventiva's ability to successfully cooperate with existing partners or enter into new partnerships, and to fulfill its obligations under any agreements entered into in connection with such partnerships, the benefits of its existing and future partnerships on the clinical development, regulatory approvals and, if approved, commercialization of its product candidates, and the achievement of milestones thereunder and the timing thereof, Inventiva and its partners may encounter substantial delays beyond expectations in their clinical trials or fail to demonstrate safety and efficacy to the satisfaction of applicable regulatory authorities, the ability of Inventiva and its partners to recruit and retain patients in clinical studies, enrollment and retention of patients in clinical trials is an expensive and time-consuming process and could be made more difficult or rendered impossible by multiple factors outside Inventiva's and its partners' control, Inventiva's product candidates may cause adverse drug reactions or have other properties that could delay or prevent their regulatory approval, or limit their commercial potential, Inventiva faces substantial competition and Inventiva's and its partners' business, and pre-clinical studies and clinical development programs and timelines, its financial condition and results of operations could be materially and adversely affected by changes in law and regulations, unfavorable conditions in its industry, geopolitical events, such as the conflict between Russia and Ukraine and related sanctions, the conflict in the Middle East and the related risk of a larger conflict, health epidemics, and macroeconomic conditions, including developments in international trade policies, global inflation, financial and credit market fluctuations, tariffs and other trade barriers, political turmoil and natural catastrophes, uncertain financial markets and disruptions in banking systems. The review of potential financial and strategic options may not result in any particular action or transaction being pursued, entered into or consummated, and there is no assurance as to the timing, sequence or outcome of any action or transaction or series of actions or transactions. Given these risks and uncertainties, no representations are made as to the accuracy or fairness of such forward-looking statements, forecasts, and estimates. Furthermore, forward-looking statements, forecasts and estimates only speak as of the date of this press release. Readers are cautioned not to place undue reliance on any of these forward-looking statements. Please refer to the Universal Registration Document for the year ended December 31, 2024, filed with the Autorité des Marchés Financiers on April 15, 2025, and the Annual Report on Form 20-F for the year ended December 31, 2024, filed with the Securities and Exchange Commission (the 'SEC') on April 15, 2025 for other risks and uncertainties affecting Inventiva, including those described under the caption 'Risk Factors' and in future filings with the SEC. Other risks and uncertainties of which Inventiva is not currently aware may also affect its forward-looking statements and may cause actual results and the timing of events to differ materially from those anticipated. All information in this press release is as of the date of the release. Except as required by law, Inventiva has no intention and is under no obligation to update or review the forward-looking statements referred to above. Consequently, Inventiva accepts no liability for any consequences arising from the use of any of the above statements. Attachment Inventiva - PR - Leadership Team Changes- EN - 07 09 2025Sign in to access your portfolio

Is Novo Nordisk Increasing Dosage to Defend Wegovy's Edge in Obesity?
Is Novo Nordisk Increasing Dosage to Defend Wegovy's Edge in Obesity?

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Is Novo Nordisk Increasing Dosage to Defend Wegovy's Edge in Obesity?

Novo Nordisk NVO announced that it has submitted a regulatory application to the European Medicines Agency (EMA) seeking approval for a new and higher dose of its popular obesity medication, Wegovy (subcutaneous semaglutide 7.2 mg). Wegovy is also indicated for major adverse cardiovascular events risk reduction, improvements in HFpEF-related symptoms and physical function, as well as pain reduction related to knee osteoarthritis. Novo Nordisk also markets semaglutide as Ozempic injection and Rybelsus oral tablet for type II diabetes (T2D). The EMA submission is backed by data from the STEP UP and STEP UP T2D studies, which evaluated semaglutide 7.2 mg in obese adult patients, with and without T2D. In the STEP UP study, the higher dose of Wegovy led to an average weight loss of 21%, with one-third of participants shedding at least 25% of their body weight compared with placebo. The 7.2 mg dose was well-tolerated and demonstrated a favorable safety profile, aligning with that of the 2.4 mg dose and previous semaglutide studies. Novo Nordisk submitted the 7.2 mg dose of Wegovy to offer a tailored option for people with obesity who need greater weight loss support. It is designed to enhance both weight reduction and related health outcomes, such as cardiovascular and kidney function, liver disease, T2D and mobility issues linked to knee osteoarthritis. Backed by a reaffirmed safety and tolerability profile, the company believes the new dose has strong potential to benefit a broader patient population, thereby expanding its reach. Novo Nordisk also plans to submit the Wegovy 7.2 mg dose for the obesity indication across several other geographies. Eli Lilly LLY is NVO's fierce competitor in the obesity space, which markets its tirzepatide medicines as Mounjaro for T2D and Zepbound for obesity. NVO's latest EMA submission for the Wegovy 7.2 mg dose is also to tackle the increasing competition from LLY's Zepbound. Lilly's Zepbound had earlier outperformed Novo Nordisk's Wegovy (20.2% compared with 13.7%, respectively) in a weight-loss head-to-head study. Despite being on the market for less than three years, Lilly's Mounjaro and Zepbound have witnessed strong sales driven by rapid demand. Several other companies, like Viking Therapeutics VKTX, are also making rapid progress in the development of GLP-1-based candidates in their clinical pipeline. Viking Therapeutics' dual GIPR/GLP-1 receptor agonist, VK2735, is being developed both as oral and subcutaneous formulations for the treatment of obesity. Recently, Viking Therapeutics initiated a late-stage program (VANQUISH), comprising two phase III studies evaluating the subcutaneous version of VK2735 in obesity and T2D patients. VKTX had also initiated a mid-stage study (VENTURE) on the oral formulation of the candidate earlier this year. Year to date, Novo Nordisk shares have lost 19% compared with the industry's 1.2% decline. The company has also underperformed the sector and the S&P 500 during the same time frame, as seen in the chart below. Image Source: Zacks Investment Research Novo Nordisk is trading at a premium to the industry, as seen in the chart below. Going by the price/earnings ratio, the company's shares currently trade at 16.33 forward earnings, which is higher than 14.93 for the industry. However, the stock is trading much below its five-year mean of 29.25. Image Source: Zacks Investment Research Earnings estimates for 2025 have improved from $3.89 to $3.93 per share over the past 60 days. During the same time frame, Novo Nordisk's 2026 earnings per share estimates have decreased from $4.70 to $4.58. Image Source: Zacks Investment Research The stock's return on equity on a trailing 12-month basis is 80.95%, which is higher than 33.55% for the large drugmaker industry, as seen in the chart below. Image Source: Zacks Investment Research Novo Nordisk currently carries a Zacks Rank #3 (Hold). You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here. Want the latest recommendations from Zacks Investment Research? Today, you can download 7 Best Stocks for the Next 30 Days. Click to get this free report Novo Nordisk A/S (NVO) : Free Stock Analysis Report Eli Lilly and Company (LLY) : Free Stock Analysis Report Viking Therapeutics, Inc. (VKTX) : Free Stock Analysis Report This article originally published on Zacks Investment Research ( Zacks Investment Research

Okay, Do I Really Need a Bath Water Filter?
Okay, Do I Really Need a Bath Water Filter?

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Okay, Do I Really Need a Bath Water Filter?

Fact checked by Sarah Scott Many of us filter our tap water for better health, safety reasons, or because we prefer the taste. But it may surprise you that some people use a filter for their bath water, especially when they have young kids who take frequent baths. Using a bath water filter isn't for everyone but experts say it may have benefits, especially for little ones with sensitive skin. Let's take a close look at bath water filters—what they are, how they work, and whether using one is a good idea for your family. So, how exactly do you filter the water that goes into your bath? Most bath water filters on the market are quite simple, actually. They are small devices that you hang on your bathtub faucet, so that the water gets filtered as it flows into your bathtub. 'Bath water filters are devices designed to remove or reduce contaminants from tap water used in bathtubs,' explains David T. Dyjack, CIH, chief executive director at National Environmental Health Association. 'They typically attach to the faucet or sit in the tub and filter out unwanted biological and chemical contaminants.' Bath water filters are relatively easy to use, says Kelly Russum, owner of KC's 23 ½ Hour Plumbing & Air Conditioning, and a plumber with 46+ years experience. 'You just attach the filter to your tub spout every time you're going to use it, and before the water fills the bathtub, it passes through the media, becoming gentler and lower on chlorine on the output.' There are several different contaminants that bath water filters can potentially filter. While not all bath filters work the same, according to Dr. Dyjack, bath water filters may be able to filter out unwanted biological and chemical contaminants, including: Chlorine, a chemical added by public water facilities to disinfect water Chloramines, used to disinfect drinking water Heavy metals, such as lead Volatile organic compounds (VOCs) like benzene, toluene. and xylene Sediment and rust Some bacteria and other impurities, though this depends on the filtering type Bath water filters aren't for everyone, but they may have benefits for certain children, and for other members of the family, says Joshua R. Resa, MD, pediatrician at Hoag Medical Group. 'For children, especially those with sensitive skin or conditions such as eczema, using a bath filter may help reduce irritation or dryness,' he explains. Filtered bath water can also be helpful for children with allergies, or whose skin is just generally sensitive. On a broader note, using bath water filters can potentially improve water quality and reduce your exposure to certain unwanted chemicals. 'While not essential for every home, it's a simple step that may help support skin health and comfort,' Dr. Resa says. According to Dr. Dyjack, other potential benefits are that bath water filters may limit the inhalation of chlorine vapors during a warm bath or shower. Additionally, though there isn't hard evidence for this, manufacturers of bath filters say their customers report softer skin and hair, Dr. Dyjack notes. Finally, bath water filters may offer peace of mind for families who live with older plumbing or who live in areas with questionable water infrastructure, says Dr. Dyjack. Bath water filters aren't perfect, and they aren't for everyone. One downside of using one is that it will end up taking longer to draw your child's bath. "The drawbacks of using bath water filters are more about inconvenience—and the main one is time,' Russum says. 'If you use a bath water filter, you need to reduce the flow, meaning it might now take two times as long to fill your tub.' As Dr. Dyjack shares, other potential drawback include: Their effectiveness is limited. 'Bath filters don't purify water to the same extent as whole-house or drinking water systems/filters do,' Dr. Dyjack explains. 'They typically reduce (not eliminate) contaminants.' They require maintenance, as the filters need to be replaced every two or three months. Many aren't effective against microbial contaminants. Okay, so what's the bottom line here? Should you run out and buy a bath filter for your family? Is it actually necessary? Bath water filters may be a good idea if you have a child with sensitive skin or a skin condition like eczema, says Dr. Resa. Reducing exposure to irritants like chlorine can be helpful there. 'That said, they're not essential for every household,' Dr. Resa emphasizes. 'Prioritizing regular skin care and hydration remains key to keeping children's skin healthy, whether or not a filter is used.' If serious larger-scale filtering is what you are looking for, you might want to consider alternatives like a full-house or RO water purification system, says Russum. These are much more thorough and effective than bath water filters that you attach to your faucet. But they are also much more expensive. A bath water filter might be something to try if you or your child takes frequent baths and has sensitive skin. 'Filters can be particularly helpful for children with eczema, sensitive, or easily irritated skin, especially if you notice dryness or irritation after bathing,' Dr. Resa shares. 'If you're unsure, it's always a good idea to consult a pediatrician or dermatologist who can provide personalized guidance based on your child's specific needs.' Keep in mind that not all bath filters are the same. These are Dr. Dyjack's tips for selecting a reliable bath water filter: Pick a filter that's NSF-certified (the gold standard) Choose a filter that clearly states it removes chlorine and chloramines Select one that offers easy installation and filter replacement Make sure filter replacements are easy to purchase, as they'll need to be replaced every few months Read the original article on Parents

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