AACE Releases Updated Guidance on Dyslipidemia Drug Therapy

AACE Releases Updated Guidance on Dyslipidemia Drug Therapy

The American Association of Clinical Endocrinology (AACE) has introduced a new guideline for managing dyslipidemia, which refers to abnormal cholesterol levels. This guideline provides evidence-based recommendations for newer drug therapies and emphasizes patient-centered outcomes, particularly the reduction of cardiovascular disease (CVD) risk. It is intended for adults aged 18 and older who have dyslipidemia or high triglycerides and are already receiving standard treatment but may need additional medications.

FDA Clears Brentuximab Combo for Advanced Large B-Cell Lymphoma Treatment

FDA Clears Brentuximab Combo for Advanced Large B-Cell Lymphoma Treatment

The U.S. Food and Drug Administration (FDA) has given the green light to a new combination therapy for adults suffering from specific types of relapsed or hard-to-treat large B-cell lymphomas (LBCL) who are not suitable candidates for stem cell transplants or CAR-T therapy. This innovative treatment consists of brentuximab vedotin (Adcetris), lenalidomide, and rituximab (BV+R2). It specifically targets types of LBCL such as diffuse large B-cell lymphoma (DLBCL), high-grade B-cell lymphoma, and DLBCL that arises from slower-growing lymphoma.

FDA Approves ADCETRIS® Combination Therapy for Relapsed/Refractory Diffuse Large B-Cell Lymphoma

FDA Approves ADCETRIS® Combination Therapy for Relapsed/Refractory Diffuse Large B-Cell Lymphoma

The U.S. Food and Drug Administration (FDA) has approved a new treatment regimen that includes Pfizer’s ADCETRIS® (brentuximab vedotin) for patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). This is an important development as it provides a new option for individuals who have not responded to at least two previous therapies and are not candidates for more aggressive treatments such as stem cell transplantation or CAR T-cell therapy.

FDA Expands IZERVAY™ Approval for Long-Term Geographic Atrophy Treatment

FDA Expands IZERVAY™ Approval for Long-Term Geographic Atrophy Treatment

The US FDA has approved a new expanded label for Astellas Pharma’s IZERVAY™ (avacincaptad pegol intravitreal solution) to treat geographic atrophy (GA) due to age-related macular degeneration (AMD) long-term. The expansion provides physicians and patients with more options for treating this progressive and chronic eye disease, which can cause irreversible vision loss.