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Putting Heavy into Heavy Slow Resistance

Further experience with the use of anti-CD38 antibodies in RRMM after prior treatment with daratumumab will stem from a current phase Ib trial of SC isatuximab in combination with Pd (NCT04045795) and for daratumumab from a phase II study in combination with Kd (NCT03871829)

It was authorized for marketing in the United States in 2023 following its designation as a Breakthrough Device by the US Food and Drug Administration and remains the only clinically validated, non-pharmaceutical treatment available for patients with RLS

In fact, gluten-dependent subepithelial deposits involving IgA-tTG are among the hallmark markers for early CD, even in seronegative patients and before histological damage occurs

doi:10.1101/gad.927301

Graduate Subspecialty and Perceptions of Cardiothoracic Surgery Training: A 60-Year Retrospective Study