{"id":62485,"date":"2024-01-11T09:00:44","date_gmt":"2024-01-11T14:00:44","guid":{"rendered":"https:\/\/www.singlecare.com\/blog\/?p=62485"},"modified":"2025-01-09T10:20:35","modified_gmt":"2025-01-09T15:20:35","slug":"upcoming-fda-approvals","status":"publish","type":"post","link":"https:\/\/www.singlecare.com\/blog\/upcoming-fda-approvals\/","title":{"rendered":"10 new drugs expected to make waves in 2025"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The drug development pipeline for 2025 looks promising, with several new medications set to hit pharmacy shelves. These upcoming treatments may help tackle a range of health issues, from <\/span><a href=\"https:\/\/www.singlecare.com\/blog\/tag\/cancer\/\"><span style=\"font-weight: 400;\">cancer<\/span><\/a><span style=\"font-weight: 400;\"> to rare genetic disorders.<\/span> <span style=\"font-weight: 400;\">Some notable drugs to watch include new cancer treatments like ivonescimab for non-small cell lung cancer and potential breakthroughs for chronic pain and hemophilia.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">As artificial intelligence increasingly influences drug development, pharmacists may see faster rollouts of personalized treatments. This shift could mean more tailored dosing and better drug safety profiles for patients.\u00a0<\/span><\/p>\n<h2 id=\"10-potential-upcoming-fda-approvals-for-2025\"><span style=\"font-weight: 400;\">10 potential upcoming FDA approvals for 2025<\/span><\/h2>\n<p><span style=\"font-weight: 400;\">Read on for some of the newest drugs that could transform patient care and improve health outcomes in the coming years.<\/span><\/p>\n<h3 id=\"ivonescimab-for-pd-l1-positive-nsclc\"><span style=\"font-weight: 400;\">Ivonescimab for PD-L1 positive NSCLC<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Ivonescimab is making waves as a promising new treatment for PD-L1 positive non-small cell lung cancer (NSCLC). This drug has shown noteworthy results in clinical trials,<\/span> <a href=\"https:\/\/www.onclive.com\/view\/ivonescimab-outperforms-pembrolizumab-as-frontline-therapy-in-pd-l1-advanced-nsclc\"><span style=\"font-weight: 400;\">outperforming the current standard of care, pembrolizumab<\/span><\/a><span style=\"font-weight: 400;\">. In a recent phase 3 study, ivonescimab reduced the risk of disease progression or death by 49% compared to pembrolizumab.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">The drug is expected to seek FDA approval in 2025. Its distinct mechanism of action involves dual targeting of both PD-1 and VEGF pathways to attack cancer cells. In addition, strong clinical results make it a particularly attractive option in <\/span><a href=\"https:\/\/www.singlecare.com\/conditions\/lung-cancer-treatment-and-medications\"><span style=\"font-weight: 400;\">lung cancer treatment<\/span><\/a><span style=\"font-weight: 400;\">.<\/span><\/p>\n<h3 id=\"cagrisema-for-obesity\"><span style=\"font-weight: 400;\">CagriSema for obesity<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">CagriSema is a new weight-loss drug that&#8217;s getting a lot of attention. It combines two active ingredients\u2014semaglutide (found in Ozempic) and cagrilintide\u2014and is expected to be <\/span><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/37364590\/\"><span style=\"font-weight: 400;\">more powerful<\/span><\/a><span style=\"font-weight: 400;\"> than current obesity treatments.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Novo Nordisk, the company behind CagriSema, plans to finish important clinical trials soon. Results from one large study are due by the end of 2024, with another coming in early 2025. If these go well, CagriSema could hit the market in late 2025. Early tests show it might help people <\/span><a href=\"https:\/\/www.reuters.com\/business\/healthcare-pharmaceuticals\/novo-nordisk-says-its-experimental-drug-cagrisema-has-similar-side-effects-2024-11-06\/\"><span style=\"font-weight: 400;\">lose up to 25%<\/span><\/a><span style=\"font-weight: 400;\"> of their body weight, which is pretty impressive. This new drug could be an advanced option for treating <\/span><a href=\"https:\/\/www.singlecare.com\/blog\/news\/weight-loss-statistics\/\"><span style=\"font-weight: 400;\">obesity<\/span><\/a><span style=\"font-weight: 400;\">.<\/span><\/p>\n<h3 id=\"suzetrigine-for-moderate-to-severe-acute-pain\"><span style=\"font-weight: 400;\">Suzetrigine for moderate-to-severe acute pain<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Suzetrigine is set to shake up pain management in 2025. The FDA has given it priority review, with a <\/span><a href=\"https:\/\/news.vrtx.com\/news-releases\/news-release-details\/vertex-announces-fda-acceptance-new-drug-application-suzetrigine\"><span style=\"font-weight: 400;\">target action date<\/span><\/a><span style=\"font-weight: 400;\"> of January 30, 2025. This new drug works by blocking sodium channels in nerve cells, offering a new method to manage pain.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">What&#8217;s exciting is that suzetrigine could be the first new class of acute pain medicine in over 20 years. It&#8217;s shown promise in clinical trials, with positive results in three Phase 3 studies and <\/span><a href=\"https:\/\/www.tandfonline.com\/doi\/full\/10.1080\/17581869.2024.2421749\"><span style=\"font-weight: 400;\">two Phase 2 studies<\/span><\/a><span style=\"font-weight: 400;\"> for moderate-to-severe acute pain. The drug has also been well-tolerated by patients, which is a plus.<\/span><\/p>\n<h3 id=\"enhertu-for-her2-low-or-her2-ultralow-metastatic-breast-cancer\"><span style=\"font-weight: 400;\">Enhertu for HER2-low or HER2-ultralow metastatic breast cancer<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Enhertu (trastuzumab deruxtecan) is making waves in breast cancer treatment. It&#8217;s under<\/span> <a href=\"https:\/\/www.astrazeneca.com\/media-centre\/press-releases\/2024\/enhertu-granted-priority-review-us-for-patients-her2-low-or-her2-ultralow-metastatic-breast-cancer-who-have-received-at-least-1-line-endocrine-therapy.html\"><span style=\"font-weight: 400;\">Priority Review by the FDA<\/span><\/a><span style=\"font-weight: 400;\"> for patients with HER2-low or HER2-ultralow metastatic breast cancer who&#8217;ve had at least one round of endocrine therapy. This drug is a big deal because it targets cancers that were tough to treat before.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Enhertu works by delivering cancer-killing drugs right to the tumor cells. In a recent study, it<\/span> <a href=\"https:\/\/www.astrazeneca.com\/media-centre\/press-releases\/2024\/Enhertu-demonstrated-median-progression-free-survival-thirteen-months.html\"><span style=\"font-weight: 400;\">showed remarkable results<\/span><\/a><span style=\"font-weight: 400;\">, keeping cancer at bay for about 13 months in patients with HR-positive, HER2-low <\/span><a href=\"https:\/\/www.singlecare.com\/conditions\/metastatic-breast-cancer-symptoms\"><span style=\"font-weight: 400;\">metastatic breast cancer<\/span><\/a><span style=\"font-weight: 400;\">. That&#8217;s a lot better than standard chemo. With potential FDA approval on the horizon, Enhertu could be a useful option for many breast cancer patients in 2025.<\/span><\/p>\n<h3 id=\"fitusiran-for-hemophilia\"><span style=\"font-weight: 400;\">Fitusiran for hemophilia<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Fitusiran is a new drug that might change how we treat hemophilia A and B. The<\/span> <a href=\"https:\/\/hemophilianewstoday.com\/news\/fda-reviewing-fitusiran-application-hemophilia-a-b-with-without-inhibitors\/\"><span style=\"font-weight: 400;\">FDA is considering its approval<\/span><\/a><span style=\"font-weight: 400;\">, which may be decided by March 28, 2025. This drug works for both types of hemophilia, even in people with inhibitors.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Sanofi, the company making fitusiran, says it&#8217;s given as a shot under the skin once a month. In a large study, people who got fitusiran had <\/span><a href=\"https:\/\/publications.aap.org\/aapgrandrounds\/article-abstract\/50\/3\/35\/193729\/Fitusiran-Prophylaxis-Reduces-Bleeding-in\"><span style=\"font-weight: 400;\">fewer bleeding episodes<\/span><\/a><span style=\"font-weight: 400;\"> than those using other treatments. The average was just 1.7 bleeds per year. This could be great news for people with hemophilia who want an easier way to manage their condition.<\/span><\/p>\n<h3 id=\"sebetralstat-for-hereditary-angioedema-hae-attacks\"><span style=\"font-weight: 400;\">Sebetralstat for hereditary angioedema (HAE) attacks<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Sebetralstat is a new oral drug that&#8217;s expected to change how <\/span><a href=\"https:\/\/www.dermatologyadvisor.com\/news\/sebetralstat-effective-for-on-demand-treatment-of-hereditary-angioedema-attacks\/\"><span style=\"font-weight: 400;\">hereditary angioedema (HAE) attacks<\/span><\/a><span style=\"font-weight: 400;\"> are treated. It&#8217;s taken as needed when an attack starts, offering a more convenient option than current injected or infused treatments. The FDA might approve it in June 2025, which would be exciting news for HAE patients.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">This drug works by<\/span> <a href=\"https:\/\/www.jacionline.org\/article\/S0091-6749(23)02391-6\/fulltext\"><span style=\"font-weight: 400;\">blocking plasma kallikrein<\/span><\/a><span style=\"font-weight: 400;\">, a key factor in HAE attacks. In a recent study, sebetralstat helped people feel better faster than a placebo. The<\/span> <a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa2314192\"><span style=\"font-weight: 400;\">300 mg and 600 mg doses both worked well<\/span><\/a><span style=\"font-weight: 400;\">, giving quick relief from HAE symptoms. This drug is appealing because it could let people treat attacks at home without needles.<\/span><\/p>\n<h3 id=\"cardamyst-for-psvt\"><span style=\"font-weight: 400;\">Cardamyst for PSVT<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Cardamyst (etripamil) is a promising new drug for treating paroxysmal supraventricular tachycardia (PSVT). The FDA is reviewing the New Drug Application for Cardamyst, with a target decision date of <\/span><a href=\"https:\/\/www.globenewswire.com\/news-release\/2024\/11\/12\/2979320\/0\/en\/Milestone-Pharmaceuticals-Reports-Third-Quarter-2024-Financial-Results-and-Provides-Regulatory-and-Corporate-Update.html\"><span style=\"font-weight: 400;\">March 27, 2025<\/span><\/a><span style=\"font-weight: 400;\">. This nasal spray could offer PSVT patients a quick and easy way to manage their symptoms at home.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Positive results from the pivotal Phase 3 RAPID trial demonstrated that etripamil, the active ingredient in Cardamyst, was twice as effective and three times as fast as a placebo in restoring normal heart rhythm. Specifically, <\/span><a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC11216497\/\"><span style=\"font-weight: 400;\">64.3% of etripamil patients<\/span><\/a><span style=\"font-weight: 400;\"> experienced PSVT termination within 30 minutes compared with 31.2% of placebo patients. Milestone Pharmaceuticals is the company behind Cardamyst.<\/span><\/p>\n<h3 id=\"moderna-s-combined-covid-19-and-flu-vaccine\"><span style=\"font-weight: 400;\">Moderna\u2019s combined COVID-19 and flu vaccine<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Moderna&#8217;s new combo shot could make getting yearly vaccines much easier. The company has created a single vaccine that protects against both <\/span><a href=\"https:\/\/investors.modernatx.com\/news\/news-details\/2024\/Moderna-RD-Day-Highlights-Progress-and-Strategic-Priorities\/default.aspx\"><span style=\"font-weight: 400;\">COVID-19 and the flu<\/span><\/a><span style=\"font-weight: 400;\">. If it gets FDA approval, this 2-in-1 jab might hit pharmacies in 2025.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">In the Phase 3 study, the combo vaccine worked better than getting separate flu and COVID shots. It sparked a stronger immune response in adults over 50. The vaccine uses mRNA technology, which helps the body make its virus-fighting proteins. A combined vaccine could be a helpful option for busy folks who don&#8217;t want to schedule multiple vaccine appointments.<\/span><\/p>\n<h3 id=\"sunlenca-for-long-acting-hiv-prevention-treatment\"><span style=\"font-weight: 400;\">Sunlenca for long-acting HIV prevention treatment<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Sunlenca (lenacapavir) is a promising new drug for HIV prevention. It&#8217;s a twice-yearly injection that could be a game-changer for people who struggle with daily pills. In a recent trial, Sunlenca was <\/span><a href=\"https:\/\/clinicalinfo.hiv.gov\/en\/drugs\/lenacapavir-hiv-prevention\"><span style=\"font-weight: 400;\">96% effective in preventing HIV infection<\/span><\/a><span style=\"font-weight: 400;\">.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">The FDA might approve Sunlenca for HIV prevention by 2025. It&#8217;s already approved for <\/span><a href=\"https:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/label\/2022\/215973s000lbl.pdf\"><span style=\"font-weight: 400;\">treating HIV<\/span><\/a><span style=\"font-weight: 400;\"> in some people. This drug works differently from other HIV meds. It&#8217;s a capsid inhibitor, which means it stops the virus from making copies of itself. For people who can&#8217;t or prefer not to take daily pills, Sunlenca could be a great option to stay HIV-negative.<\/span><\/p>\n<h3 id=\"ozempic-for-chronic-kidney-disease\"><span style=\"font-weight: 400;\">Ozempic for chronic kidney disease<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Ozempic (semaglutide) might soon be used to treat <\/span><a href=\"https:\/\/www.singlecare.com\/blog\/chronic-kidney-disease\/\"><span style=\"font-weight: 400;\">chronic kidney disease<\/span><\/a><span style=\"font-weight: 400;\"> in people with Type 2 diabetes. This popular diabetes drug has shown promise in slowing kidney disease progression.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A recent study found that Ozempic reduced the risk of kidney complications and heart issues in people with Type 2 diabetes and <\/span><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/38785209\/\"><span style=\"font-weight: 400;\">chronic kidney disease<\/span><\/a><span style=\"font-weight: 400;\">. The drug cut the risk of kidney disease-related events by 24% compared to a placebo. Ozempic works by mimicking a hormone that regulates blood sugar and appetite. The FDA is now reviewing an application to expand Ozempic&#8217;s use for kidney disease. If approved, it could offer a new treatment option for millions of people with this condition.<\/span><\/p>\n<h3 id=\"zepbound-for-obstructive-sleep-apnea\"><span style=\"font-weight: 400;\">Zepbound for obstructive sleep apnea<\/span><\/h3>\n<p><span style=\"font-weight: 400;\">Zepbound (tirzepatide) might soon help people with <\/span><a href=\"https:\/\/www.singlecare.com\/conditions\/sleep-apnea-treatment-and-medications\"><span style=\"font-weight: 400;\">sleep apnea<\/span><\/a><span style=\"font-weight: 400;\"> breathe easier at night. Eli Lilly expects the FDA to decide on approving this drug for obstructive sleep apnea by early 2025. This is big news because Zepbound works differently than current sleep apnea treatments. It helps people lose weight, which may, in turn, help improve breathing during sleep.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Recent studies have shown promising results for Zepbound. It<\/span> <span style=\"font-weight: 400;\">effectively resolved sleep apnea, reducing the <\/span><a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa2404881\"><span style=\"font-weight: 400;\">Apnea-Hypopnea Index (AHI)<\/span><\/a><span style=\"font-weight: 400;\"> by 20.0 events per hour in trial 1 and 23.8 events per hour in trial 2. This drug could be a useful treatment for those struggling with both obesity and sleep apnea, as it provides a new way to manage these linked health issues with just one medication.<\/span><\/p>\n<h2 id=\"looking-ahead\"><span style=\"font-weight: 400;\">Looking ahead<\/span><\/h2>\n<p><span style=\"font-weight: 400;\">The year 2025 is set to be noteworthy for new drug approvals, with many innovative medicines in development. Key focus areas include cancer treatments, pain management, heart disease therapies, and rare disease drugs. Suzetrigine, in particular, could revolutionize pain management, while other medications like Ozempic are being explored for new potential uses, such as managing chronic kidney disease. While the FDA&#8217;s thorough approval process can take years, it can ultimately bring new treatment options for patients and healthcare providers alike.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The drug development pipeline for 2025 looks promising, with several new medications set to hit pharmacy shelves. These upcoming treatments may help tackle a range of health issues, from cancer to rare genetic disorders. Some notable drugs to watch include new cancer treatments like ivonescimab for non-small cell lung cancer and potential breakthroughs for chronic [&hellip;]<\/p>\n","protected":false},"author":135,"featured_media":62423,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[9340],"tags":[4141,743,7],"coauthors":[8669],"class_list":["post-62485","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-the-checkout","tag-fda-approvals","tag-pharmacies","tag-singlecare","wpautop"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.4 (Yoast SEO v27.4) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Upcoming FDA approvals expected in 2025<\/title>\n<meta name=\"description\" content=\"Stay ahead of the curve! 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