Publications by authors named "R Ward Hagar"
Etavopivat is an investigational, once daily, oral, selective erythrocyte pyruvate kinase (PKR) activator. A multicenter, randomized, placebo-controlled, double-blind, 3-part, phase 1 study was conducted to characterize the safety and clinical activity of etavopivat. Thirty-six patients with sickle cell disease (SCD) were enrolled into 4 cohorts: 1 single-dose, 2 multiple ascending doses, and 1 open-label (OL).
View Article and Find Full Text PDFArticle Synopsis
- Renewable energy development is crucial for meeting global energy needs and addressing climate change, but its effects on wildlife need further investigation.
- Traditional methods for identifying bird species from collected samples can miss many due to difficulties in recognizing partial remains, or "feather spots."
- A DNA barcoding technique utilizing mitochondrial genetic data was successfully applied to identify bird samples from solar facilities, improving the accuracy of wildlife impact assessments and enabling better comparisons across different energy projects.
Background: Patients with sickle cell disease (SCD) have a unique form of cardiomyopathy. However, left ventricular ejection fraction (LVEF) is often preserved. Monoplanar long-axis strain (LAS) can be assessed from MRI four-chamber views and may be better at detecting mild systolic dysfunction in these patients.
View Article and Find Full Text PDFObjectives: L-Glutamine was FDA-approved for sickle cell disease (SCD) in 2017, yet the mechanism(s)-of-action are poorly understood. This study investigates the potential activation of autophagy as a previously unexplored mechanism-of-benefit.
Design: Prospective, open-label, 8-week, phase-2 trial of oral L-glutamine (10 g TID) in patients with SCD at risk for pulmonary hypertension identified by Doppler-echocardiography by an elevated tricuspid-regurgitant-jet-velocity (TRV)≥ 2.
Objectives: L-Glutamine is FDA-approved for sickle cell disease (SCD), yet the mechanism(s)-of-action are poorly understood. We performed a pharmacokinetics (pK) study to determine the metabolic fate of glutamine supplementation on plasma and erythrocyte amino acids in patients with SCD.
Design: A pK study was performed where patients with SCD fasting for > 8 h received oral L-glutamine (10 g).