ReportGem ReportGem EN

普通外文研报

US Biopharmaceuticals: Reminder: Expert call on Agios’ AQVESME launch in thalassemia; TODAY at 10am ET

发布日期: 2026-06-08研究机构: BofA Global Research报告页数: 4原文语言: 英语证据页码: 1

研报英文原文证据摘录

US Biopharmaceuticals: Reminder: Expert call on Agios’ AQVESME launch in thalassemia; TODAY at 10am ET

Accessible version

US Biopharmaceuticals

Reminder: Expert call on Agios’ AQVESME

launch in thalassemia; TODAY at 10am ET

Invitation

Topic 08 June 2026

With the AQVESME launch now underway in thalassemia, we hope to provide an updated Equity

perspective on real-world uptake, early physician and patient experience, and the United States

practical considerations shaping intended use. We are hosting a conference call with Dr. Biopharmaceuticals

Sujit Sheth, MD, Chief of Pediatric Hematology/Oncology at Weill Cornell Medicine and

Related ResearchNewYork-Presbyterian Hospital, who currently manages ~250 thalassemia patients.

We will discuss Dr. Sheth’s hands-on AQVESME experience (as an investigator on the Agios Pharmaceuticals: Tebapivat LR-MDS miss

ENERGIZE studies and in the commercial setting), including patient selection, response narrows AGIO focus to thal launch and SCD

expectations, monitoring logistics, and how REMS requirements are affecting treatment readouts

initiation and follow-up in the U.S. The discussion will also touch on how labeling and Agios Pharmaceuticals: EU thalassemia

access considerations may differ outside the U.S., including markets without a approved without REMS; further validates

launch trajectorymandatory REMS program, and what that could imply for labeling/adoption over time. Agios Pharmaceuticals: Solid demand signals

More broadly, we will discuss how AQVESME may fit into the evolving thalassemia in thalassemia, SCD a larger debate with

treatment landscape alongside supportive care, luspatercept, and potentially curative sNDA filing in 2Q26e

approaches including gene therapy and gene editing. Agios Pharmaceuticals: Etavopivat topline data

本摘录由系统从所标注的 PDF 证据页直接提取并保留英文原文,不做批量翻译;登录后在阅读器切换中文时才按需翻译。

打开研报阅读器