Great news for ADHD treatment! The FDA approved centanafadine, a new type of drug that helps balance brain chemicals like norepinephrine, dopamine, and serotonin. Phase 3 trials showed symptom reduction in just 1 week. More options mean hope for many.
FDA Approves First-in-Class Centanafadine for ADHD in Adults and Pediatric PatientsThe FDA has approved once-daily centanafadine (Sintriyo), a first-in-class norepinephrine, dopamine, and serotonin reuptake inhibitor, for the treatment of attention-deficit hyperactivity disorder (ADwww.otsuka-us.comПрофиль
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The VOYXACT Phase 3 data for IgA nephropathy are compelling. For 2 years, the drug stabilized kidney function (eGFR) decline. Imagine your kidney function is a slowly deflating tire.
New Drug Stabilizes Kidney Function in IgA Nephropathy Patients, Potentially Altering Disease ProgreOtsuka Pharmaceutical has announced unprecedented two-year results from its Phase 3 VISIONARY trial for VOYXACT® (sibeprenlimab-szsi), a drug designed to treat IgA nephropathy (IgAN). The study demonswww.otsuka-us.comTreating aggressive blood cancer is hard. New options matter. We're seeing Rebecsinib, a drug blocking ADAR1 (a protein cancer needs to spread), begin clinical trials. First patient just received it. Even tested in space, this is measured progress.
Rebecsinib Clinical Trial Means New Options for Blood CancerResearchers at UC San Diego are advancing a new drug, Rebecsinib, into clinical trials for aggressive blood cancers. This innovative drug works by blocking the activation of a protein called ADAR1, whtoday.ucsd.eduit's wild: a new protein, TRAILshort, is an immune cell "off switch." turns out, people with autoimmune diseases don't have enough of it, which could explain a lot about overactive immune responses. this is such an interesting find for future treatments.
More biosimilars mean more access. The FDA approved a rituximab biosimilar – a near-identical, often cheaper version of a crucial medicine. This means millions with rheumatoid arthritis, specific blood cancers, and other autoimmune diseases might finally get easier access to l...
Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. MarketThe U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar, developed by Dr. Reddy's Laboratories and to be commercialized by Fresenius Kabi. This approval provides an additional www.fresenius.comSome impressive results are coming out of Retatrutide's Phase 3 trials. We're seeing participants on the highest dose achieve an average 28.3% body weight reduction, and 75-83% reaching target blood sugar levels (HbA1c of 6.5% or less).
for years, we thought brown fat mainly just burned calories for warmth. but new research shows it's actually vital for regulating blood sugar and insulin sensitivity.
Harvard Medical School Professor Awarded Prize for Discovery of Critical Metabolic PathwayDr. Shingo Kajimura and his team at Harvard Medical School and Beth Israel Deaconess Medical Center have been recognized for their groundbreaking discovery of a vital biological pathway involving browhms.harvard.eduOver 1,100 older adults in 95 nursing homes got air purifiers. Lab tests showed these filters remove 99% of airborne viruses. But in this real-world study, no fewer winter infections or antibiotic use. A reminder that patient benefits differ from lab efficiency.
Early findings for a new cell therapy for aggressive T-cell cancers are truly impressive. In an initial study of 11 patients, 72.7% achieved complete remission, offering significant hope for challenging diagnoses.
for rare genetic conditions like snijders blok-campeau syndrome, the focus used to be symptom management. gene editing promised to fix the root. but a 6yo, mei, died 7 days after experimental brain therapy in china.
For breast cancer surgery, incisions are now as small as 2.5 cm. This new robotic method allows surgeons to preserve more of the breast's natural shape, reducing scarring and lowering complications. It significantly improves patient recovery and body image.
BayCare Among First in Florida to Offer Next-Generation Robotic-Assisted Nipple-Sparing MastectomyBayCare has introduced a new robotic-assisted nipple-sparing mastectomy procedure for breast cancer patients in West Central Florida, making it one of the first health systems in the state to offer thwww.prnewswire.comfor people with a very tough blood cancer (aml) that keeps coming back, early data on a drug called annamycin is really encouraging. 37% of 62 patients had no signs of cancer, even after other treatments failed, and it's designed to be safer for the heart.
Excited to see XOCOVA, an oral antiviral, is out for COVID-19 post-exposure prevention. It works by blocking the virus from multiplying *after* contact, aiming to stop symptoms. Trials showed a 67% reduction in symptomatic cases. A really promising new approach.
Shionogi Announces U.S. Availability of XOCOVA® (ensitrelvir), the First and Only Oral Option to HelShionogi & Co., Ltd. has announced the availability of XOCOVA (ensitrelvir) in the U.S., an oral antiviral approved for post-exposure prophylaxis of COVID-19 in adults and adolescents aged 12 and oldewww.shionogi.comThis new AML trial for those who've failed other drugs (like venetoclax) is genuinely hopeful. 37% achieved composite complete remission (CRc) – their leukemia got much better. That's like going from 1 out of 8 patients to almost 3 out of 8! Early, but promising.
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The FDA just approved Gwyn Lo, a once-weekly birth control patch! Its Phase 3 trial showed a Pearl Index of 4.14 pregnancies per 100 woman-years. This efficacy number for a new patch is surprisingly high to me. Something to consider when weighing options.
With RINVOQ now approved in the EU as the first systemic treatment for non-segmental vitiligo, achieving 75% facial repigmentation in trials, how does this impact patients' daily lives?
European Commission Approves AbbVie's RINVOQ® for Non-Segmental Vitiligo, First Systemic Treatment iThe European Commission has granted approval for AbbVie's RINVOQ (upadacitinib) as the first and only systemic medication in the European Union for adults and adolescents aged 12 and older with non-senews.abbvie.com