SEEKING BIOTECH ALPHA = BIOTECMAX
THE HEART OF BIOTEC 12/7/2025
SEEKING BIOTECH ALPHA = BIOTECMAX
THE HEART OF BIOTEC 12/7/2025
SEEKING BIOTECH ALPHA = BIOTECMAX
THE HEART OF BIOTEC 12/7/2025
SEEKING BIOTECH ALPHA = BIOTECMAX
THE HEART OF BIOTEC 12/7/2025
SEEKING BIOTECH ALPHA = BIOTECMAX
THE HEART OF BIOTEC 12/7/2025
biotecHEART™
biotecHEART-information/data on Heart related medications
Baxdrostat demonstrated a statistically significant and highly clinically meaningful placebo-adjusted reduction of 14.0 mmHg in 24-hour ambulatory systolic blood pressure in patients with resistant hypertension in the Bax24 Phase III trial PUBLISHED 9 November 2025 Baxdrostat demonstrated a statistically significant placebo-adjusted reduction of 13.9 mmHg in night-time ambulatory systolic blood pressure at 12 weeks with a safety profile consistent with the BaxHTN trial Full results presented at the American Heart Association Scientific Sessions 2025 Positive full results from the Bax24 Phase III trial showed baxdrostat demonstrated a statistically significant and highly clinically meaningful reduction in ambulatory 24-hour average systolic blood pressure (SBP) compared with placebo at 12 weeks. Patients with treatment-resistant hypertension (rHTN) received baxdrostat 2mg or placebo on top of standard of care.1 Efficacy was observed throughout the 24-hour period, including early morni
REPATHA® NOW INDICATED FOR ADULTS AT INCREASED RISK FOR MAJOR ADVERSE CARDIOVASCULAR EVENTS DUE TO UNCONTROLLED LDL-C THOUSAND OAKS, Calif., Aug. 25, 2025 /PRNewswire/ -- Amgen (NASDAQ:AMGN) today announced that the U.S. Food and Drug Administration (FDA) has broadened the approved use of Repatha® (evolocumab) to include adults at increased risk for major adverse cardiovascular events (MACE) due to uncontrolled low-density lipoprotein cholesterol (LDL-C), commonly known as 'bad cholesterol.' The update removes a prior requirement for a patient to have been diagnosed with cardiovascular (CV) disease.
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