Findings showed both zanidatamab treatment arms demonstrated statistically significant and clinically meaningful improvements in PFS vs the SOC arm.

Immigration experts warn the policy could make it easier for officers to deny visas based on their own judgment.

The sNDA was supported by data from a 4 week MUSE study and a long-term open-label study in children aged 2 to 5 years.

The indication was restricted to only patients with DMD who are 4 years of age and older with a confirmed mutation in the DMD gene; the indication for non-ambulatory patients with DMD was removed.

Tyruko ® (natalizumab-sztn), a biosimilar to Tysabri ® (natalizumab), has been made available by Sandoz, according to developer Polpharma Biologics.

Nonopioids are noninferior on days 2 and 3 and during the postoperative period; higher patient satisfaction reported with nonopioids.

The allergy develops after a bite from the Lone Star tick, which can make the body react to alpha-gal, a sugar found in beef, pork, lamb and other mammalian meats. Many people experience hives, nausea ...

HealthDay News — Commonly used noncancer medications, including proton pump inhibitors, are associated with poorer survival and adverse events for patients with breast cancer, according to a study ...

Naphazoline HCl 0.025%, pheniramine maleate 0.3%; oph. soln; contains benzalkonium chloride. Avoid prolonged use. Narrow-angle glaucoma. Hypertension. Cardiovascular disease. Urinary hesitancy.

The phase 3 Librexia ACS trial evaluating the safety and efficacy of milvexian after a recent acute coronary syndrome has been discontinued.

Poherdy can be dispensed as a substitute for Perjeta without requiring a prescription change from a health care provider.

The FDA requests boxed warnings be removed from HRT product labels; Caplyta approved for MDD; Darzalex Faspro gains new indication; investigational MS treatment looks promising; trial investigates ...