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- An FDA advisory panel voted 10-3 on Thursday in favor of Replimune Group's experimental melanoma treatment, RP1.
- The committee concluded that efficacy results from the company's IGNYTE clinical trial were both evaluable and clinically meaningful.
- This positive recommendation significantly increases the likelihood of FDA approval following two previous rejections of the therapy.
- The decision marks a critical step forward for Replimune Group in bringing its specialized cancer treatment to the market.
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Medical Bulletin 31/July/2026
• A new AI tool called MEDWACS has been developed to identify undiagnosed individuals with type 2 diabetes using over 30 years of U.S. health data. • The findings, published in the Journal of Clinical Epidemiology, highlight the tool's ability to detect the disease before patients seek medical testing.
Read original · medicaldialogues.inFederal government could improve infectious disease monitoring, says federal government
• The nominee for the director of the Centers for Disease Control and Prevention (CDC) has advanced to a full Senate vote. • The federal government indicated that Medicaid work requirements will not be delayed, maintaining current policy timelines.
Read original · statnews.com
StatnewsFlorida Investigates Fauci; Obesity Drug Trial Sparks Lawsuit; 'Early Bird' Dinners
• The FTC and multiple states are suing telehealth company Hims & Hers for allegedly sharing sensitive patient health data with third-party advertisers. • Novo Nordisk is facing a shareholder lawsuit claiming the company misled investors regarding clinical trial results for its investigational weight-loss drug, CagriSema.
Read original · medpagetoday.com
MedPage TodayFDA panel endorses Replimune's previously rejected melanoma drug
• An FDA advisory committee has voted in favor of RP1, an experimental melanoma drug developed by Replimune, despite the therapy being rejected in April. • The decision comes during a review meeting where experts evaluated the drug's efficacy and safety for treating melanoma patients.
Read original · statnews.com
StatnewsMonday, July 27, 2026 - KFF Health News
• The FDA’s Pharmacy Compounding Advisory Committee has approved the peptides epitalon and semax for compounding. • Medical experts warn that this decision may mislead the public into believing the FDA has thoroughly evaluated the safety and efficacy of these compounds.
Read original · kffhealthnews.orgI’m a Doctor Who Treated Measles in the 2015 Outbreak. 7 Things People Keep Getting Wrong
• An infectious disease specialist is debunking common misconceptions about measles as U.S. cases reach a 35-year high. • The doctor draws on professional experience treating patients during the 2014-2015 Disneyland outbreak, which spread across six U.S. states and into Canada.
Read original · today.com
TODAY.comSARS-CoV-2 Point-of-Care Testing Modalities: Integrating Molecular, Immunological, Biosensor, and AI Approaches
• The COVID-19 pandemic underscored an urgent requirement for rapid, accurate, and accessible diagnostic tools to improve clinical decision-making and public health surveillance. • Point-of-care testing (POCT) has become a vital component of decentralized healthcare, allowing for diagnostic procedures to be performed outside of traditional laboratory environments.
Read original · mdpi.com“Tipping Point”: Ex-CDC Official Links Cyclospora & Measles Outbreaks to Trump’s Public Health Cuts
• Former CDC chief medical officer Debra Houry links current outbreaks of measles and foodborne cyclosporiasis to significant public health funding cuts. • Houry resigned from her position one year ago to protest political interference and the leadership of HHS Secretary Robert F. Kennedy Jr.
Read original · democracynow.org
Democracy Now!More than 12 million eye drops recalled nationwide over contamination fears that could harm vision
• The FDA has issued a Class II recall for more than 12 million eye drops nationwide due to contamination concerns. • The recall was triggered by fears that the contaminated products could cause temporary damage to users' eyes or vision.
Read original · dailymail.com
Mail OnlineFeds shut down ‘dangerous’ gain-of-function research, tighten oversight of foreign collaboration
• The Trump administration has implemented a new policy ending federal support for "dangerous" gain-of-function (DGOF) research. • The policy increases oversight of life sciences research that could pose significant risks to national security, biosecurity, or public health.
Read original · cidrap.umn.eduResearch updates, July 28 - The Sick Times
• A study published in Neurophysiologie Clinique found that 50 individuals with Long COVID exhibited persistent neuromuscular abnormalities. • Researchers used two types of electromyography tests to provide objective measurements of muscle function, offering a potential biological marker for the condition.
Read original · thesicktimes.org
The Sick Times

