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Fulcrum Therapeutics to Present at the 31st Annual FSHD Society International Research Congress

Fulcrum Therapeutics to Present at the 31st Annual FSHD Society International Research Congress

fulcrum therapeutics將在第31屆FSHD協會國際研究大會上發表演講
GlobeNewswire ·  06/12 20:00

CAMBRIDGE, Mass., June 12, 2024 (GLOBE NEWSWIRE) -- Fulcrum Therapeutics, Inc. (the "Company") (Nasdaq: FULC), a clinical-stage biopharmaceutical company focused on developing small molecules to improve the lives of patients with genetically defined rare diseases, today announced upcoming presentations to be made at the 31st Annual FSHD Society International Research Congress being held June 13-14, 2024 in Denver, Colorado, including an abstract outlining the baseline characteristics of patients enrolled in the Phase 3 REACH trial of losmapimod in facioscapulohumeral muscular dystrophy (FSHD).

美國馬薩諸塞州劍橋市,2024年6月12日(GLOBE NEWSWIRE)——fulcrum therapeutics董事會(Nasdaq: FULC)宣佈,該公司將在2024年6月13日至14日舉行的第31屆FSHD學會國際研究大會上做出即將到來的演講,這包括一篇摘要,概述了losmapimod在面部、肩胛骨和上臂肌肉萎縮症(FSHD)3期REACH試驗中,患者基線特徵的情況。作爲一家臨床階段生物製藥公司,fulcrum therapeutics專注於開發小分子藥物,改善患有基因定義罕見疾病的患者的生活。(納斯達克:FULC)21世紀醫療改革法案本次演講的主題如下:

The presentations to be made are as follows:

所做的演講如下所示:

Title: Characteristics of the Enrolled Population in the Phase 3 REACH Trial in Facioscapulohumeral Muscular Dystrophy (FSHD)
Poster Number: P7.01
Format: Poster
First Author: Nicol Voermans, MD, PhD, Radboud University Medical Center
Presentation Date and Time: Thursday, June 13, 2024, between 5:30-8:30 PM MDT

題目:面部、肩胛骨和上臂肌肉萎縮症(FSHD)3期REACH試驗中受試者群體的特徵
海報編號:P7.01
格式:海報
第一作者:Nicol Voermans, MD, PhD,Radboud大學醫學中心
演示日期和時間:2024年6月13日星期四,MDT時間下午5:30至8:30之間

Title: Facioscapulohumeral Muscular Dystrophy (FSHD) Disease Progression and Losmapimod Efficacy Assessed by Reachable Workspace in Both Arms
Presentation Number: S6.06
Format: Oral presentation
Presenter: Joost Kools, MD, Radboud University Medical Center
Presentation Date and Time: Friday, June 14, 2024 at 3:50 PM MDT

題目:通過可達工作區域評估面部、肩胛骨和上臂肌肉萎縮症(FSHD)疾病進展和Losmapimod療效
演講編號:S6.06
格式:口頭報告
演講者:Joost Kools, MD,Radboud大學醫學中心
演講日期和時間:2024年6月14日星期五下午3:50 MDT

Title: Safety and Tolerability of Losmapimod for the Treatment of FSHD
Poster Number: P6.05
Format: Poster
First Author: Mihaela Levitchi Benea, MD, Executive Director of Medical Affairs at Fulcrum Therapeutics
Presentation Date and Time: Thursday, June 13, 2024, between 5:30-8:30 PM MDT

題目:Losmapimod治療FSHD的安全性和耐受性
海報編號:P6.05
格式:海報
第一作者:Mihaela Levitchi Benea, MD,fulcrum therapeutics醫學事務執行主任
演示日期和時間:2024年6月13日星期四,MDT時間下午5:30至8:30之間

Title: Reliability and Validity of Reachable Workspace Total Score with Wrist Weights in
Facioscapulohumeral Muscular Dystrophy
Poster Number: P7.06
Format: Poster
First Author: Lena Hubig, Acaster Lloyd Consulting
Presentation Date and Time: Thursday, June 13, 2024, between 5:30-8:30 PM MDT

題目:使用手腕重量對可達工作區域總分數的可靠性和有效性進行評估
肌肉萎縮性側腹肌肌 dystrophy
海報編號:P7.06
格式:海報
第一作者:Lena Hubig,阿卡斯特洛伊德諮詢
演示日期和時間:2024年6月13日星期四,MDT時間下午5:30至8:30之間

The presentation and posters will be available on the publications page of Fulcrum's website at

演示和海報可在Fulcrum網站的出版物頁面上進行查看

About Fulcrum Therapeutics
Fulcrum Therapeutics is a clinical-stage biopharmaceutical company focused on developing small molecules to improve the lives of patients with genetically defined rare diseases in areas of high unmet medical need. Fulcrum's two lead programs in clinical development are losmapimod, a small molecule in development for the treatment of facioscapulohumeral muscular dystrophy (FSHD), and pociredir, a small molecule designed to increase expression of fetal hemoglobin and in development for the treatment of sickle cell disease (SCD) and other hemoglobinopathies. Fulcrum uses proprietary technology to identify drug targets that can modulate gene expression to treat the known root cause of gene mis-expression. For more information, visit and follow us on Twitter/X (@FulcrumTx) and LinkedIn.

Fulcrum Therapeutics是一家臨床階段的生物製藥公司,專注於開發小分子化合物,改善遺傳定義罕見病領域的高度醫療需求患者的生活質量。Fulcrum在臨床開發中的兩個主要項目是losmapimod,一種用於治療面肌肩帶肌肌肉萎縮症(FSHD)的小分子化合物,以及pociredir,一種設計用於增加胎兒血紅蛋白表達並用於治療鐮狀細胞病(SCD)和其他血紅蛋白病的小分子化合物。Fulcrum使用專有技術識別藥物靶點,以調節基因表達來治療已知的基因錯配根本原因。有關更多信息,請訪問並在Twitter/X上關注我們(@FulcrumTx)和LinkedIn。
Fulcrum Therapeutics是一家臨床階段的生物製藥公司,致力於開發小分子藥物,改善罕見遺傳性疾病患者在高度未滿足醫療需求領域的生活質量。Fulcrum的兩個領先臨床開發項目是losmapimod,一種小分子藥物,用於治療肌肉萎縮性側腹肌肌萎縮症(FSHD),以及pociredir,一種小分子藥物,旨在增加胎兒血紅蛋白的表達,並用於治療鐮狀細胞貧血症(SCD)和其他血紅蛋白病。Fulcrum使用專有技術識別可調節基因表達以治療已知基因錯配根本原因的藥物靶點。欲了解更多信息,請訪問網站並關注我們的Twitter / X(@ FulcrumTx)和LinkedIn。

Contact:
Chris Calabrese
LifeSci Advisors, LLC
ccalabrese@lifesciadvisors.com
917-680-5608

聯繫方式:
Chris Calabrese
LifeSci Advisors,LLC
ccalabrese@lifesciadvisors.com
917-680-5608


譯文內容由第三人軟體翻譯。


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