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Applied Therapeutics to Sponsor and Present at the 2022 Galactosemia Foundation Conference

Applied Therapeutics to Sponsor and Present at the 2022 Galactosemia Foundation Conference

應用治療公司贊助並出席2022年半乳糖症基金會會議
GlobeNewswire ·  2022/07/28 19:27
  • Gold sponsor of the 2022 Galactosemia Foundation Conference; new website and educational resources as part of ongoing commitment to the Galactosemia community
  • Applied Therapeutics to present research and clinical update
  • 2022年半乳糖症基金會會議的黃金贊助商;新的網站和教育資源,作為對半乳糖症社區持續承諾的一部分
  • 應用治療學呈現研究和臨牀最新進展

NEW YORK, July 28, 2022 (GLOBE NEWSWIRE) -- Applied Therapeutics, Inc. (Nasdaq: APLT), a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need, today announced its sponsorship and presentations at the 2022 Galactosemia Foundation Conference being held July 28-30 in Orlando, Florida.

紐約,2022年7月28日(環球網)--臨牀階段生物製藥公司應用治療公司(納斯達克代碼:APLT)今天宣佈贊助2022年半乳糖症基金會會議,並在7月28-30日在佛羅裏達州奧蘭多舉行的2022年半乳糖症基金會會議上發表演講。該公司正在開發一系列針對高度未得到滿足的醫療需求的已驗證分子靶標的新型候選藥物。

"We are proud to be a gold sponsor of the Galactosemia Foundation Conference, and to sponsor the Galactosemia Foundation's new website and educational resources to help families navigate the challenges of living with Galactosemia," said Shoshana Shendelman, PhD, CEO, Founder and Chair of the Board of Applied Therapeutics. "The Galactosemia Conference is a unique event, bringing together patients, families, and researchers to work together towards a shared goal of improving the lives of patients with Galactosemia."

Shoshana Shendelman博士、首席執行官、應用治療委員會主席Shoshana Shendelman説:“我們很榮幸成為半乳糖症基金會會議的黃金贊助商,並贊助半乳糖症基金會的新網站和教育資源,以幫助家庭應對半乳糖症患者的挑戰。半乳糖症會議是一次獨特的活動,將患者、家屬和研究人員聚集在一起,朝着改善半乳糖症患者生活的共同目標而努力。

"Galactosemia is a serious progressive disease that significantly impacts quality of life. Long-term complications are caused by galactitol, a toxic metabolite of galactose," said Riccardo Perfetti, MD, PhD, Chief Medical Officer of Applied Therapeutics. "We look forward to providing the community with an update on our research at the conference, and express our deep appreciation to the patients, families and researchers who have made this work possible."

應用治療公司首席醫療官裏卡多·佩爾菲蒂説:“半乳糖血症是一種嚴重的進行性疾病,嚴重影響生活質量。長期的併發症是由半乳糖的有毒代謝物半乳糖醇引起的。”我們期待着在會議上向社會提供我們研究的最新情況,並對使這項工作成為可能的患者、家屬和研究人員表示深切的感謝。

"Applied Therapeutics is a strong partner to the Galactosemia community and the Galactosemia Foundation. We are excited to launch our new website and resources at the Galactosemia Conference, which would not have been possible without the support of Applied Therapeutics," said Nicole Casale, President of the Galactosemia Foundation.

“應用治療公司是半乳糖症社區和半乳糖症基金會的強大合作伙伴。我們很高興能在半乳糖症會議上推出我們的新網站和資源,如果沒有應用治療公司的支持,這是不可能的,”半乳糖症基金會的妮可·卡薩萊、總裁説。

Applied Therapeutics Presentation Details

應用治療學演示文稿詳情

Presentation: Applied Therapeutics Update
Shoshana Shendelman, PhD, CEO and Founder, Applied Therapeutics
Date and Time: Friday, July 29, 2022, 11:30 AM EST

演示文稿:應用治療學最新進展
Shoshana Shendelman,博士,應用治療公司首席執行官兼創始人
日期和時間:美國東部時間2022年7月29日星期五上午11:30

Presentation: ACTION-Galactosemia Clinical Program Update
Shoshana Shendelman, PhD, CEO and Founder, Applied Therapeutics; Riccardo Perfetti, MD, PhD, Chief Medical Officer, Applied Therapeutics; Evan Bailey, MD, Executive Medical Director, Applied Therapeutics
Date and Time: Friday, July 29, 2022, 1:30 PM EST

演示文稿:行動-半乳糖血症臨牀方案更新
應用治療公司首席執行官和創始人Shoshana Shendelman博士;應用治療公司首席醫療官Riccardo Perfetti醫學博士;應用治療公司董事執行醫學博士Evan Bailey
日期和時間:美國東部時間2022年7月29日星期五下午1:30

Meet-the-Expert Panel
Riccardo Perfetti, MD, PhD, Chief Medical Officer, Applied Therapeutics; Laura Saltonstall, MD, MBA, Vice President of Medical Affairs, Applied Therapeutics; Evan Bailey, MD, Executive Medical Director, Applied Therapeutics
Date and Time: Saturday, July 30, 2022, 1:30 PM EST

專家見面會
應用治療公司首席醫療官裏卡多·佩爾菲蒂,醫學博士,博士;應用治療公司醫療事務副主任,醫學博士,工商管理碩士勞拉·薩爾頓斯托爾;應用治療公司醫學董事執行董事,埃文·貝利
日期和時間:美國東部時間2022年7月30日星期六下午1:30

For additional information on the Galactosemia Conference and to register, please visit: app.mobilecause.com/e/9g0ESQ?vid=rf10s 

有關半乳糖症會議和註冊的更多信息,請訪問:app.mobilecause.com/e/9g0ESQ?vid=rf10s

To access the Galactosemia Foundation's new website and resources, please visit:  

要訪問半乳糖症基金會的新網站和資源,請訪問:

About AT-007

關於AT-007

AT-007 is a central nervous system (CNS) penetrant Aldose Reductase inhibitor (ARI) in development for the treatment of several rare neurological diseases, including Galactosemia, SORD Deficiency, and PMM2-CDG. In clinical trials, AT-007 significantly reduced plasma galactitol levels vs. placebo in adults and children with Galactosemia. AT-007 is currently being studied in a Phase 3 clinical outcomes trial (ACTION-Galactosemia Kids) in children ages 2-17 with Galactosemia, as well as a long-term open-label study in adults with Galactosemia. In a pilot study, AT-007 significantly reduced blood sorbitol levels in adults with SORD Deficiency. AT-007 is currently being studied in a Phase 3 trial (INSPIRE) investigating biomarker efficacy, clinical outcomes, and significantly reduced blood sorbitol levels in adults with SORD Deficiency. AT-007 has received both Orphan Drug and Pediatric Rare Disease designations from the U.S. Food and Drug Administration (FDA) for the treatment of Galactosemia and PMM2-CDG, and Fast Track designation for Galactosemia.

AT-007是一種中樞神經系統(CNS)穿透性醛糖還原酶抑制劑(ARI),正在開發中,用於治療幾種罕見的神經系統疾病,包括半乳糖血症、SORD缺乏症和PMM2-CDG。在臨牀試驗中,與安慰劑相比,AT-007顯著降低了患有半乳糖血症的成人和兒童的血漿半乳糖醇水平。AT-007目前正在進行一項針對2-17歲半乳糖血症兒童的3期臨牀結果試驗(ACTION-半乳糖血症兒童),以及一項針對患有半乳糖血症的成人的長期開放式研究。在一項初步研究中,AT-007顯著降低了SORD缺乏症成年人的血液山梨醇水平。AT-007目前正在進行3期試驗(INSPIRE)研究,調查SORD缺乏症成年人的生物標記物療效、臨牀結果和顯著降低的血液山梨醇水平。AT-007已經獲得了美國食品和藥物管理局(FDA)對治療半乳糖症和PMM2-CDG的孤兒藥物和兒科罕見疾病的指定,以及對半乳糖症的快速跟蹤指定。

About Applied Therapeutics

關於應用治療學

Applied Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need. The Company's lead drug candidate, AT-007, is a novel central nervous system penetrant Aldose Reductase Inhibitor (ARI) for the treatment of CNS rare metabolic diseases, including Galactosemia, SORD Deficiency, and PMM2-CDG. The Company is also developing AT-001, a novel potent ARI, for the treatment of Diabetic Cardiomyopathy, or DbCM, a fatal fibrosis of the heart. The preclinical pipeline also includes AT-003, an ARI designed to cross through the back of the eye when dosed orally, for the treatment of Diabetic retinopathy, as well as novel dual PI3k inhibitors in preclinical development for orphan oncology indications.

應用治療公司是一家臨牀階段的生物製藥公司,針對高度未得到滿足的醫療需求的適應症,針對經過驗證的分子靶標開發一系列新藥候選藥物。該公司的主要候選藥物AT-007是一種新型中樞神經系統穿透性醛糖還原酶抑制劑(ARI),用於治療中樞神經系統罕見的代謝性疾病,包括半乳糖血症、SORD缺乏症和PMM2-CDG。該公司還在開發AT-001,一種新的有效的ARI,用於治療糖尿病心肌病(DbCM),這是一種致命的心臟纖維化。臨牀前流水線還包括AT-003,一種口服時可穿過眼後部的ARI,用於治療糖尿病視網膜病變,以及用於孤兒腫瘤學適應症的臨牀前開發的新型雙PI3K抑制劑。

To learn more, please visit and follow the company on Twitter @Applied_Tx.

欲瞭解更多信息,請訪問並關注該公司的Twitter@Applied_TX。

Forward-Looking Statements

前瞻性陳述

This press release contains "forward-looking statements" that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact, included in this press release regarding strategy, future operations, prospects, plans and objectives of management, including words such as "may," "will," "expect," "anticipate," "plan," "intend," and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are forward-looking statements. Forward-looking statements in this release involve substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by the forward-looking statements, and we, therefore cannot assure you that our plans, intentions, expectations, or strategies will be attained or achieved.

本新聞稿包含“前瞻性陳述”,這些陳述涉及根據1995年“私人證券訴訟改革法”提供的安全港所涉及的重大風險和不確定性。本新聞稿中包含的關於戰略、未來業務、前景、計劃和管理目標的任何陳述,除有關歷史事實的陳述外,包括“可能”、“將會”、“預期”、“預期”、“計劃”、“打算”和類似的表述(以及涉及未來事件、條件或情況的其他詞語或表述)都是前瞻性表述。本新聞稿中的前瞻性陳述涉及大量風險和不確定性,可能導致實際結果與前瞻性陳述中明示或暗示的結果大不相同,因此我們不能向您保證我們的計劃、意圖、期望或戰略一定會實現或實現。

Such risks and uncertainties include, without limitation, factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in our filings with the U.S. Securities and Exchange Commission, including the "Risk Factors" contained therein. Except as otherwise required by law, we disclaim any intention or obligation to update or revise any forward-looking statements, which speak only as of the date they were made, whether as a result of new information, future events or circumstances or otherwise.

此類風險和不確定因素包括但不限於可能導致實際結果與本新聞稿中的前瞻性陳述中明示或暗示的結果不同的因素,這些因素在我們提交給美國證券交易委員會的文件中進行了討論,包括其中包含的“風險因素”。除非法律另有要求,否則我們沒有任何更新或修改任何前瞻性陳述的意圖或義務,這些前瞻性陳述僅在作出之日發表,無論是由於新信息、未來事件或情況或其他原因。

Contacts

聯繫人

Investors:

投資者:

Maeve Conneighton
(212) 600-1902
appliedtherapeutics@argotpartners.com

梅芙·康希頓
(212) 600-1902
郵箱:AppliedTreateutics@argopartners.com

Media:

媒體:

media@appliedtherapeutics.com

郵箱:Media@AppliedTreateutics.com

Applied Therapeutics, Inc.

應用治療公司


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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