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		<title>Concord Biotech jumps 8% on USFDA nod for Mycophenolate Mofetil oral suspension</title>
		<link>https://lsd.hu/concord-biotech-jumps-8-on-usfda-nod-for-mycophenolate-mofetil-oral-suspension/</link>
		
		<dc:creator><![CDATA[LSD News Szerkesztőség]]></dc:creator>
		<pubDate>Wed, 03 Jun 2026 05:59:13 +0000</pubDate>
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		<category><![CDATA[Biotech]]></category>
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		<category><![CDATA[Concord Biotech]]></category>
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					<description><![CDATA[Shares of Concord Biotech surged as much as 8.46% on Wednesday, hitting an intraday high of Rs 1,264.90, after the company announced that it had received approval from the U.S. Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Mycophenolate Mofetil for Oral Suspension USP, 200 mg/mL. According to the company&#8217;s [&#8230;]]]></description>
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<div data-brcount="15">Shares of Concord Biotech surged as much as 8.46% on Wednesday, hitting an intraday high of Rs 1,264.90, after the company announced that it had received approval from the U.S. Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Mycophenolate Mofetil for Oral Suspension USP, 200 mg/mL.</p>
<p>According to the company&#8217;s regulatory filing, the approved product is an antimetabolite immunosuppressant used for the prophylaxis of organ rejection in adult and pediatric patients aged three months and older undergoing kidney, heart, or liver transplants. The medication is administered in combination with other immunosuppressive therapies.</p>
<p>The company highlighted that the approval aligns with its long-term growth strategy and is expected to strengthen its presence in the U.S. pharmaceutical market. Industry estimates suggest that the U.S. market for Mycophenolate Mofetil is valued at approximately US$30 million, providing Concord Biotech with a significant commercial opportunity.</p>
<p>In its disclosure, Concord Biotech stated that the approval was granted by the U.S. Food and Drug Administration (USFDA) and pertains specifically to Mycophenolate Mofetil for Oral Suspension USP, 200 mg/mL. The company noted that the approval will enhance its product portfolio and support expansion across both U.S. and international markets. There were no instances of withdrawal, cancellation, or suspension of the approval, and therefore no associated penalties or adverse financial impact.<b></p>
<h2>Stock Performance and Valuation</h2>
<p></b>Despite Tuesday&#8217;s rally, Concord Biotech&#8217;s stock remains significantly below its 52-week high of Rs 2,150. The stock&#8217;s 52-week low stands at Rs 987. The company currently commands a market capitalization of approximately Rs 12,200 crore.</p>
<p>On the valuation front, the stock is trading at a price-to-earnings (P/E) ratio of 42.56 and a price-to-book (P/B) ratio of 6.13.<b></p>
<h2>Technical Indicators</h2>
<p></b>The stock&#8217;s Relative Strength Index (RSI-14) stands at 56.2, indicating neutral-to-positive momentum. An RSI reading below 30 is generally considered oversold, while a reading above 70 signals overbought conditions.</p>
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<div class="imgBox"><img decoding="async" alt="ET logo" src="https://img.etimg.com/photo/118783427.cms" width="90%" title="Concord Biotech jumps 8% on USFDA nod for Mycophenolate Mofetil oral suspension 2"></div>
<h3 class="logoTitle">Live Events</h3>
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<p>From a trend perspective, Concord Biotech is trading above six of its eight key simple moving averages (SMAs), reflecting a broadly positive technical setup.<b></p>
<h2>Shareholding Pattern</h2>
<p></b>Institutional investor activity remained mixed during the March 2026 quarter. Foreign Institutional Investors (FIIs) marginally increased their stake in Concord Biotech to 7.79% from 7.58% in the previous quarter, reflecting continued investor interest. In contrast, mutual funds trimmed their holdings, reducing their stake from 4.44% to 4.30% during the same period.</p>
<p>(Disclaimer: Recommendations, suggestions, views and opinions given by the experts are their own. These do not represent the views of The Economic Times)</p></div>
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		<title>Eli Lilly&#8217;s obesity pill remains a viable rival to Novo&#8217;s oral Wegovy despite data that underwhelmed investors</title>
		<link>https://lsd.hu/eli-lillys-obesity-pill-remains-a-viable-rival-to-novos-oral-wegovy-despite-data-that-underwhelmed-investors/</link>
		
		<dc:creator><![CDATA[LSD News Szerkesztőség]]></dc:creator>
		<pubDate>Sun, 24 Aug 2025 20:56:42 +0000</pubDate>
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		<guid isPermaLink="false">https://www.lsd.hu/eli-lillys-obesity-pill-remains-a-viable-rival-to-novos-oral-wegovy-despite-data-that-underwhelmed-investors/</guid>

					<description><![CDATA[A sign with the company logo sits outside of the headquarters of Eli Lilly in Indianapolis, Indiana, on March 17, 2024. Scott Olson &#124; Getty Images Eli Lilly&#8216;s stock is still recovering after the drugmaker released trial data earlier this month on its closely watched obesity pill that underwhelmed Wall Street. In a key late-stage trial, [&#8230;]]]></description>
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<p>A sign with the company logo sits outside of the headquarters of Eli Lilly in Indianapolis, Indiana, on March 17, 2024.</p>
<p>Scott Olson | Getty Images</p>
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<p><span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-1">Eli Lilly<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span>&#8216;s stock is still recovering after the drugmaker released trial data earlier this month on its closely watched obesity pill that underwhelmed Wall Street.</p>
<p>In a key late-stage trial, Eli Lilly&#8217;s pill, orforglipron, caused less weight loss and had higher side effects than what analysts were expecting. The pill&#8217;s efficacy also appeared to come in slightly below that of <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-4">Novo Nordisk<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span>&#8216;s oral semaglutide for obesity, which showed strong data in a separate study.</p>
<p>Shares of Eli Lilly fell about 13% on the day the trial results were released, although they&#8217;re up about 12% since then.</p>
<p>But some analysts say Eli Lilly&#8217;s daily pill, if approved, could still be a viable competitor in the weight loss drug space — even if it will likely be second to enter the market. It&#8217;s a highly lucrative area that is eager for more convenient options that could ease the supply shortfalls and access hurdles created by the pricey weekly injections currently dominating it.</p>
<p>Analysts note that Eli Lilly&#8217;s pill could have a few advantages over the daily oral version of Novo Nordisk&#8217;s weight loss drug semaglutide, which is on track to become the<a href="https://www.prnewswire.com/news-releases/fda-accepts-filing-application-for-oral-semaglutide-25-mg-which-if-approved-would-be-the-first-oral-glp-1-treatment-for-obesity-302445232.html" target="_blank" rel="noopener"> first needle-free alternative</a> for obesity to win approval in the U.S. later this year. Eli Lilly hopes to launch its pill globally &#8220;this time next year,&#8221; CEO David Ricks told CNBC in early August.</p>
<p>Both drugs work by mimicking a gut hormone called GLP-1 to suppress appetite and regulate blood sugar. But while Novo Nordisk&#8217;s pill is a peptide medication, orforglipron is a small-molecule drug.</p>
<p>That means Eli Lilly&#8217;s pill is absorbed more easily in the body and doesn&#8217;t require dietary restrictions like Novo Nordisk&#8217;s does. Orforglipron will also be easier to manufacture at scale, which is crucial as demand for obesity and diabetes injections outpaces supply.</p>
<p>Neither company has released prices for its respective pill, but some analysts said Eli Lilly&#8217;s drug could potentially have a lower price than Novo Nordisk&#8217;s pill. That would be a notable edge, as many health plans in the U.S. still don&#8217;t cover obesity treatments.</p>
<p>&#8220;It&#8217;s a little bit of an apples and oranges comparison because Novo Nordisk could have difficulty manufacturing enough of the product, given the high cost and requirements to manufacture oral semaglutide,&#8221; Leerink Partners analyst David Risinger said in an interview. </p>
<p>&#8220;Whereas Lilly plans to blanket the world with orforglipron, and very quickly it will generate dramatically more sales,&#8221; he continued. &#8220;It can launch globally in an extraordinary manner with lower prices and with no food intake consideration.&#8221;</p>
<p>Goldman Sachs analysts seem to agree, based on a note in August. They forecast daily oral pills will capture 24% share — or around $22 billion — of the 2030 global weight loss drug market, which they expect to be worth $95 billion. </p>
<p>The Goldman analysts said they expect Eli Lilly&#8217;s pill to have a 60% share — or roughly $13.6 billion — of the daily oral segment of the market in 2030. They expect Novo Nordisk&#8217;s oral semaglutide to have a 21% share — or around $4 billion — of that segment. The remaining 19% slice will go to other emerging pills, the analysts said.</p>
<p>The race to develop a more convenient obesity pill has been fraught, as companies such as <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-7">Pfizer<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span> have had to scrap previous contenders and bring forward new ones. Novo Nordisk and Eli Lilly are also exploring other experimental oral drugs, along with a slate of other companies such as <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-9">Viking Therapeutics<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span>, <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-10">Structure Therapeutics<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span>, <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-11">AstraZeneca<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span> and <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-12">Roche<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span>. </p>
<p>In a statement, Novo Nordisk CEO Mike Doustar said &#8220;we strongly believe in the efficacy&#8221; of the oral drug. The Danish company added it will be &#8220;laser-focused on getting this product to patients without supply constraints&#8221; in the U.S. </p>
<p>Dr. Mihail &#8220;Misha&#8221; Zilbermint, director of endocrine hospitalists at Johns Hopkins Community Physicians, said it&#8217;s hard to crown a winner between Eli Lilly and Novo Nordisk without knowing how their respective pills will be priced and whether insurance will cover them. </p>
<p>&#8220;I think both of the drugs are going to be gamechangers,&#8221; he said. &#8220;When it comes to which company is going to win the game — cost is the biggest issue.&#8221;</p>
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<h2 class="ArticleBody-subtitle"><a id="headline0"/>Weight loss, side effect comparisons</h2>
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<p>It&#8217;s difficult to directly compare the results of separate clinical trials, especially as investors wait for Eli Lilly and Novo Nordisk to release the full data from their phase three studies.</p>
<p>Eli Lilly&#8217;s ATTAIN-1 trial also followed 3,000 patients, while Novo Nordisk&#8217;s OASIS 4 study evaluated a<a href="https://clinicaltrials.gov/study/NCT05564117" target="_blank" rel="noopener"> much smaller group </a>of roughly 300. There are currently no studies directly comparing the two drugs, a Novo Nordisk spokesperson said.</p>
<p>But Novo Nordisk&#8217;s oral semaglutide appears to cause a greater level of weight loss than Eli Lilly&#8217;s pill based on the available data, said BMO Capital Markets analyst Evan Seigerman. </p>
<p>In the trial, the highest dose of Eli Lilly&#8217;s pill helped patients lose 12.4% of their body weight on average at 72 weeks. The pill&#8217;s weight loss was 11.2% when analyzing all patients regardless of discontinuations.</p>
<p>Wall Street had hoped Eli Lilly&#8217;s pill would generate weight loss of around 15%, the same level as Novo Nordisk&#8217;s blockbuster weight loss injection Wegovy. Semaglutide is the active ingredient in Wegovy and its diabetes counterpart Ozempic. </p>
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<p>Novo Nordisk flags flutter outside its office in Bagsvaerd, on the outskirts of Copenhagen, Denmark, on July 14, 2025.</p>
<p>Tom Little | Reuters</p>
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<p>Meanwhile, the 25-milligram dose of Novo Nordisk&#8217;s oral semaglutide helped patients lose up to 16.6% of their weight on average at 64 weeks, according to results from the trial presented at a medical conference in 2024. That weight loss was 13.6% when the company analyzed all patients regardless of whether they stopped the drug. </p>
<p>A Novo Nordisk spokesperson added that 20% of weight loss was observed in nearly one-third of patients in the trial.</p>
<p>Still, the slightly lower efficacy of Eli Lilly&#8217;s pill may not be significant enough to deter patients from taking it. </p>
<p>&#8220;For many patients, 12% is a really great number,&#8221; said Seigerman. &#8220;There&#8217;s definitely a market there&#8221; for orforglipron.</p>
<p>In a note earlier this month, Bank of America analysts shared a similar sentiment. </p>
<p>&#8220;Yes, weight loss fell a bit short, but ask 100 prescribers whether this new data will really make a difference in who they&#8217;d put on orforglipron, and our belief is the vast majority would say, &#8216;not really,'&#8221; they wrote, referring to Eli Lilly&#8217;s trial data. </p>
<p>Some investors raised concerns about the side effects and discontinuation rates in the trial of Eli Lilly&#8217;s pill. But Seigerman said the drug&#8217;s tolerability data — how well patients tolerate it — appears to be relatively in line with that of Novo Nordisk&#8217;s oral semaglutide. </p>
<p>About 10.3% of patients who took the highest dose of Eli Lilly&#8217;s pill — 36 milligrams — discontinued treatment due to side effects, compared with around 2.6% of those who took a placebo.</p>
<p>Those side effects were mainly gastrointestinal, such as nausea and vomiting, and mild to moderate in severity. An estimated 24% of those who took the highest dose of Eli Lilly&#8217;s pill reported vomiting, while 33.7% had nausea. </p>
<p>Leerink&#8217;s Risinger said he is watching to see how persistent those gastrointestinal issues are once Eli Lilly presents the full data. </p>
<p>The side effects in the trial on Novo Nordisk&#8217;s pill were mostly gastrointestinal-related: 30.9% of those who took oral semaglutide reported vomiting and 46.6% reported nausea, according to the trial results. </p>
<p>Johns Hopkins&#8217; Zilbermint said it&#8217;s difficult for him to decide which one has a better safety and tolerability profile based on the available data. </p>
<p>Meanwhile, Seigerman pointed to a different factor &#8220;that will also matter a lot&#8221;: dietary requirements. </p>
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<h2 class="ArticleBody-subtitle"><a id="headline1"/>Food requirements, manufacturing, price </h2>
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<p>Unlike Eli Lilly&#8217;s pill, patients need to take Novo Nordisk&#8217;s oral semaglutide in the morning on an empty stomach with no more than four ounces of plain water. They&#8217;re instructed to wait 30 minutes before eating, drinking or taking other oral medicines.</p>
<p>Seigerman said that could be a hurdle for some patients. </p>
<p>For example, &#8220;if you&#8217;re a parent with kids and you have to take this drug and wait half an hour before you can drink your coffee, you&#8217;re going to drive yourself crazy, especially if you have to take this every day,&#8221; he said. &#8220;I try to think about the real-world use of these drugs in a market like this. It&#8217;s going to matter.&#8221; </p>
<p>Leerink&#8217;s Risinger said oral semaglutide will also be &#8220;extremely expensive to manufacture&#8221; since it is a peptide medication, and &#8220;is likely going to have to be priced higher than orforlipgron.&#8221;</p>
<p>A Novo Nordisk spokesperson said the pill will be made mostly in the U.S., and the company is excited about the potential the pill &#8220;provides millions of Americans living with obesity.&#8221;</p>
<p>&#8220;Currently, all typical launch readiness activities [for the pill] are fully underway and building momentum,&#8221; the spokesperson said. They added that over the past decade, the company has invested $24 billion in the U.S. to expand manufacturing capacity and fuel research and development. That includes investments aimed at increasing manufacturing of active pharmaceutical ingredients and capacity for the final stages of production for both current and future injectable and oral products. </p>
<p>Small molecules are chemically simpler and easier to produce at scale, making them generally cheaper for companies to formulate. But it is still unclear how Eli Lilly will price orforglipron. </p>
<p>During an earnings call in August, Eli Lilly&#8217;s Ricks said the pricing will be based on the value orforglipron brings, considering health-care savings and the comorbidities it can address.</p>
<p>In the note earlier this month, Goldman Sachs analysts said they expect the pill to be &#8220;priced at parity&#8221; to Eli Lilly&#8217;s tirzepatide, the active ingredient in the company&#8217;s obesity injection Zepbound and diabetes counterpart Mounjaro, which list for just over $1,000 for a month&#8217;s supply. </p>
<p>&#8220;They should be cheaper than injections because they are easier to produce. But it does not mean they will be cheaper,&#8221; Johns Hopkins&#8217; Zilbermint said. &#8220;We just don&#8217;t know — for example, we don&#8217;t know how much went into research and development.&#8221;</p>
<p>Seigerman said commercialization strategies will also be key when the pills compete on the market. </p>
<p>He questioned whether Novo Nordisk will lean into the deal it recently struck with <span class="QuoteInBody-quoteNameContainer" data-test="QuoteInBody" id="RegularArticle-QuoteInBody-14">CVS<span class="QuoteInBody-inlineButton"><span class="AddToWatchlistButton-watchlistContainer" id="-WatchlistDropdown" data-analytics-id="-WatchlistDropdown"><button class="AddToWatchlistButton-watchlistButton" aria-label="Add To Watchlist" data-testid="dropdown-btn"><span class="AddToWatchlistButton-addWatchListFromTag"/></button></span></span></span>&#8216;s pharmacy benefit manager, Caremark. Under the deal, Caremark started to prioritize Novo Nordisk&#8217;s Wegovy on its standard formularies on July 1, making that weekly injection the preferred GLP-1 drug for obesity over Zepbound. </p>
<p>But it is unclear whether oral semaglutide could receive a similar preferential status.</p>
<p>Seigerman also questioned whether Eli Lilly will offer orforglipron through its direct-to-consumer pharmacy, LillyDirect. That offering bypasses insurers and pharmacy benefit managers, allowing patients to directly purchase Zepbound and some of Eli Lilly&#8217;s other drugs from the company. </p>
<p>Seigerman said he expects &#8220;a lot of nuances in the go-to-market campaign for these drugs,&#8221; adding &#8220;that&#8217;s going to matter.&#8221;</p>
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<h2 class="ArticleBody-subtitle"><a id="headline2"/>Other competitors trail behind</h2>
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<p>Other obesity pills are in earlier stages of development, making it difficult to directly compare them to the drugs from Eli Lilly and Novo Nordisk without longer and larger trials. </p>
<p>But so far, some experts think they pale in comparison.</p>
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<p>For example, Viking Therapeutics on Tuesday released mid-stage trial data that disappointed investors, sending its stock down as much as 40%. </p>
<p>Jared Holz, Mizuho health care equity strategist, said in an email Tuesday that the results on Viking&#8217;s drug &#8220;look inferior&#8221; to those of Eli Lilly&#8217;s pill &#8220;on almost all metrics.&#8221; </p>
<p>Viking&#8217;s once-daily pill helped patients lose up to 12.2% of their weight at around three months, with no plateau, which means patients could lose even more in a longer-term study.</p>
<p>Holz pointed to the high rate of patients who discontinued Viking&#8217;s drug for any reason over 13 weeks, which was around 28%. Meanwhile, around a quarter of people discontinued Eli Lilly&#8217;s pill, orforglipron, for any reason over 72 weeks.</p>
<p>That&#8217;s &#8220;a much longer trial and therefore [Lilly] looks far better head-to-head,&#8221; Holz said.</p>
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		<title>Supreme Court set to hear oral arguments on challenge to TikTok ban</title>
		<link>https://lsd.hu/supreme-court-set-to-hear-oral-arguments-on-challenge-to-tiktok-ban/</link>
		
		<dc:creator><![CDATA[LSD News Szerkesztőség]]></dc:creator>
		<pubDate>Fri, 10 Jan 2025 04:35:19 +0000</pubDate>
				<category><![CDATA[Tech]]></category>
		<category><![CDATA[arguments]]></category>
		<category><![CDATA[Ban]]></category>
		<category><![CDATA[Breaking News: Technology]]></category>
		<category><![CDATA[business news]]></category>
		<category><![CDATA[Challenge]]></category>
		<category><![CDATA[court]]></category>
		<category><![CDATA[hear]]></category>
		<category><![CDATA[Internet]]></category>
		<category><![CDATA[oral]]></category>
		<category><![CDATA[Set]]></category>
		<category><![CDATA[Social media]]></category>
		<category><![CDATA[Supreme]]></category>
		<category><![CDATA[Technology]]></category>
		<category><![CDATA[TikTok]]></category>
		<guid isPermaLink="false">https://www.lsd.hu/supreme-court-set-to-hear-oral-arguments-on-challenge-to-tiktok-ban/</guid>

					<description><![CDATA[Tik Tok creators gather before a press conference to voice their opposition to the &#8220;Protecting Americans from Foreign Adversary Controlled Applications Act,&#8221; pending crackdown legislation on TikTok in the House of Representatives, on Capitol Hill in Washington, U.S., March 12, 2024. Craig Hudson &#124; Reuters The Supreme Court on Friday will hear oral arguments in [&#8230;]]]></description>
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<p>Tik Tok creators gather before a press conference to voice their opposition to the &#8220;Protecting Americans from Foreign Adversary Controlled Applications Act,&#8221; pending crackdown legislation on TikTok in the House of Representatives, on Capitol Hill in Washington, U.S., March 12, 2024. </p>
<p>Craig Hudson | Reuters</p>
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<p>The Supreme Court on Friday will hear oral arguments in the case involving the future of TikTok in the U.S., which could ban the popular app as soon as next week.</p>
<p>The justices will consider whether the Protecting Americans from Foreign Adversary Controlled Applications Act, the law that targets TikTok&#8217;s ban and imposes harsh civil penalties for app &#8220;entities&#8221; that continue to carry the service after Jan.19, violates the U.S. Constitution&#8217;s free speech protections.</p>
<p>It&#8217;s unclear when the court will hand down a decision, and if China&#8217;s ByteDance continues to refuse to divest TikTok to an American company, it faces a complete ban nationwide.</p>
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<h2 class="ArticleBody-subtitle"><a id="headline0"/>What will change about the user experience?</h2>
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<p>The roughly 115 million U.S. TikTok monthly active users could face a range of scenarios depending on when the Supreme Court hands down a decision.</p>
<p>If no word comes before the law takes effect on Jan. 19 and the ban goes through, it&#8217;s possible that users would still be able to post or engage with the app if they already have it downloaded. However, those users would likely be unable to update or redownload the app after that date, multiple legal experts said.</p>
<p>Thousands of short-form video creators who generate income from TikTok through ad revenue, paid partnerships, merchandise and more will likely need to transition their businesses to other platforms, like YouTube or Instagram.</p>
<p>&#8220;Shutting down TikTok, even for a single day, would be a big deal, not just for people who create content on TikTok, but everyone who shares or views content,&#8221; said George Wang, a staff attorney at the Knight First Amendment Institute who helped write the institute&#8217;s amicus briefs on the case. </p>
<p>&#8220;It sets a really dangerous precedent for how we regulate speech online,&#8221; Wang said.</p>
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<h2 class="ArticleBody-subtitle"><a id="headline1"/>Who supports and opposes the ban?</h2>
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<p>Dozens of high-profile amicus briefs from organizations, members of Congress and President-elect Donald Trump were filed supporting both the government and ByteDance.</p>
<p>The government, led by Attorney General Merrick Garland, alleges that until ByteDance divests TikTok, the app remains a &#8220;powerful tool for espionage&#8221; and a &#8220;potent weapon for covert influence operations.&#8221;</p>
<p><a href="https://www.supremecourt.gov/DocketPDF/24/24-656/336151/20241227163400981_2024-12-27%20-%20TikTok%20v.%20Garland%20-%20Amicus%20Brief%20of%20President%20Donald%20J.%20Trump.pdf" target="_blank" rel="noopener">Trump&#8217;s brief</a> did not voice support for either side, but it did ask the court to oppose banning the platform and allow him to find a political resolution that allows the service to continue while addressing national security concerns. </p>
<p>The short-form video app played a notable role in both Trump and Democratic nominee Kamala Harris&#8217; presidential campaigns in 2024, and it&#8217;s one of the most common news sources for younger voters.</p>
<p>In a September Truth Social post, Trump wrote in all caps Americans who want to save TikTok should vote for him. The post was quoted in his amicus brief. </p>
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<h2 class="ArticleBody-subtitle"><a id="headline2"/>What comes next?</h2>
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<p>It&#8217;s unclear when the Supreme Court will issue its ruling, but the case&#8217;s expedited hearing has some predicting that the court could issue a quick ruling. </p>
<p>The case will have &#8220;enormous implications&#8221; since TikTok&#8217;s user base in the U.S. is so large, said Erwin Chemerinsky, dean of Berkeley Law. </p>
<p>&#8220;It&#8217;s unprecedented for the government to prohibit platforms for speech, especially one so many people use,&#8221; Chemerinsky said. &#8220;Ultimately, this is a tension between free speech issues on the one hand and claims of national security on the other.&#8221;</p>
<p><strong>WATCH: </strong>It appears TikTok could really get shut down, says Jim Cramer</p>
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