Sydney Jennings

Takeda reported phase 3 data showing zasocitinib achieved higher week 16 PASI 100 responses than deucravacitinib in plaque psoriasis.

Late-breaking SLEEP 2026 findings bring primary-care-ready insights on insomnia drugs, sleep apnea genetics, menopausal sleep, and GLP-1 links.

SLEEP 2026: Women with moderate-to-severe obstructive sleep apnea reported worse sleep, fatigue, anxiety, headaches, and nocturia than men.

The first guideline for cardiovascular-kidney-metabolic syndrome details staging, screening, risk assessment, and treatment.

Retatrutide phase 3 trials showed reductions in weight, A1C, osteoarthritis pain, and sleep apnea severity.

New FLOW trial data presented at ERA 2026 showed semaglutide improved health-related quality of life in adults with type 2 diabetes and CKD.

Recent FDA updates include new actions in diabetes, hypertension, chronic HDV infection, bipolar depression, and CKD in type 1 diabetes.

A natural experiment found pediatric influenza vaccination reduced influenza diagnoses among children aged 2 to 5 years.

A national survey found US adults recognize STI transmission routes but remain uncertain about HPV and mpox vaccine prevention.

The FDA today issued a Complete Response Letter for Cingulate’s CTx-1301 for ADHD, citing CMC-related requests and no current safety or efficacy concerns.

FDA approved ensitrelvir for COVID-19 postexposure prophylaxis in adults and adolescents aged 12 years and older after exposure.

FDA approval expands Afrezza as an inhaled mealtime insulin option for pediatric patients with diabetes aged 6 years and older.

A national survey found high awareness of prenatal health guidance but gaps on alcohol avoidance, iron use, and gestational weight gain.

Post hoc phase 3 analyses linked centanafadine to improved executive function and emotional regulation in adults with ADHD.

ACS updated colorectal cancer screening guidance, reaffirming screening at age 45 and adding newer stool-based and blood-based options.

Elunetirom received FDA Fast Track designation as an adjunctive therapy for bipolar depression, with phase 2 AMPLIFY-BD data expected in 2026.

FDA approved bulevirtide-gmod (Hepcludex; Gilead Sciences) for adults with chronic HDV infection without cirrhosis or with compensated cirrhosis, based on phase 3 data.

Orforglipron reduced body weight versus placebo in adults aged 65 years or older with obesity or overweight in ATTAIN-1 and ATTAIN-2.

FDA grants priority review to finerenone for adults with type 1 diabetes and chronic kidney disease based on FINE-ONE data.

Retatrutide reduced body weight by up to 28.3% at 80 weeks in adults with obesity or overweight in the phase 3 TRIUMPH-1 trial.

FDA accepted Bayer's asundexian NDA for recurrent stroke prevention after noncardioembolic ischemic stroke or TIA.

A NHANES analysis suggests a ferritin cutoff below 24 μg/L may identify more iron deficiency in children aged 5 to 14 years.

Embedding addiction treatment in a resident primary care clinic increased confidence in SUD diagnosis, medication use, and harm-reduction counseling.

A Massachusetts claims study found rising pediatric primary care visits with mental health diagnoses, led by anxiety-related care.

FDA approved baxdrostat for adults with hypertension not controlled on other agents, adding a new aldosterone-targeting option.

A 5-day course of ensitrelvir reduced symptomatic COVID-19 risk by 67% after household exposure in the phase 3 SCORPIO-PEP trial.

A large claims analysis suggests most US patients with prediabetes receive annual diabetes screening, although methods were not peer reviewed.

Global experts have redefined PCOS as PMOS, spotlighting metabolic and heart risks to speed diagnosis, reduce stigma, and improve care.

MR-100A-01 weekly contraceptive patch data will be presented ahead of an FDA decision on the investigational lower-estrogen product.

South London data show stroke rates climbing again, hitting Black communities and poorer areas hardest, and exposing gaps in prevention and follow-up.