U.S. Investigator-Initiated Trial (IIT) to Evaluate Jaguar Health's Crofelemer for Short Bowel Syndrome With Intestinal Failure (SBS-IF) Begins
U.S. Investigator-Initiated Trial (IIT) to Evaluate Jaguar Health's Crofelemer for Short Bowel Syndrome With Intestinal Failure (SBS-IF) Begins
The study is one of five clinical efforts - three IIT proof-of-concept studies and two Phase 2 studies - of crofelemer for the rare disease indications of SBS-IF and/or microvillus inclusion disease (MVID), an ultrarare congenital diarrheal disorder, in the US, EU, and/or Middle East/North Africa (MENA) regions; availability of IIT proof-of-concept results potentially in Q2 2025
這項研究是關於crofelemer用於罕見疾病SBS-IF和/或微絨毛包涵體疾病(MVID)的五個臨床努力之一,包括三個IIt概念驗證研究和兩個2期研究,覆蓋美國產、歐洲及中東/北非(MENA)地域板塊;IIt概念驗證結果預計將在2025年第二季度提供。
Crofelemer, Jaguar's novel plant-based prescription drug, has been granted Orphan Drug Designation by the FDA and the European Medicines Agency for both SBS-IF and MVID
crofelemer是Jaguar公司開發的一種新型植物基處方藥,已獲得FDA和歐洲藥品管理局對SBS-IF和MVID的孤兒藥資格認證。
SAN FRANCISCO, CA / ACCESSWIRE / December 6, 2024 / Jaguar Health, Inc. (NASDAQ:JAGX) (Jaguar) family company Napo Pharmaceuticals (Napo) today announced that an independent IIT in the U.S. to evaluate the efficacy and safety of crofelemer, Jaguar's novel plant-based anti-diarrheal prescription drug, for the rare disease indication of short bowel syndrome with intestinal failure (SBS-IF) in adults has begun. An overview of the study can be viewed on the ClinicalTrials.gov website.
舊金山,加利福尼亞州 / ACCESSWIRE / 2024年12月6日 / Jaguar Health, Inc.(納斯達克:JAGX)(Jaguar)旗下公司Napo Pharmaceuticals(Napo)今天宣佈,在美國進行的一項獨立的IIt研究已經開始,旨在評估crofelemer的療效和安全性,這是Jaguar開發的一種新型植物基抗腹瀉處方藥,用於成人短腸綜合徵伴腸功能不全(SBS-IF)的罕見疾病指徵。該研究的概述可在ClinicalTrials.gov網站上瀏覽。
Lisa Conte, Jaguar's founder, president, and CEO, said, "This study is one of five clinical efforts - three IIT proof-of-concept studies and two Phase 2 studies - of crofelemer for the rare disease indications of SBS-IF and/or MVID in the US, European Union, and/or MENA regions. These studies are evaluating a novel powder formulation of crofelemer for oral solution - which is different from the FDA-approved oral formulation of crofelemer available for people living with HIV/AIDS. Dosing of the first patient in each of these five studies is expected to occur throughout December 2024 and Q1 2025, with availability of IIT proof-of-concept results potentially in Q2 2025. In accordance with the guidelines of specific EU countries, published data from clinical investigations in SBS-IF and MVID could support reimbursed early patient access to crofelemer for these debilitating conditions in those countries."
Lisa Conte,Jaguar的創始人、總裁和首席執行官表示:"這項研究是關於crofelemer用於罕見疾病SBS-IF和/或MVID的五個臨床努力之一,包括三個IIt概念驗證研究和兩個2期研究,覆蓋美國、歐洲聯盟和中東/北非(MENA)地域板塊。這些研究正在評估crofelemer的新型粉末配方口服溶液——這一配方不同於FDA批准的針對HIV/AIDS患者的口服配方。預計將於2024年12月和2025年第一季度進行這五項研究的首位患者的給藥,並且IIt概念驗證結果預計將在2025年第二季度提供。根據特定歐盟國家的指南,關於SBS-IF和MVID的臨床研究發佈的數據可能支持這些國家對crofelemer的早期報銷患者接入。"
"SBS-IF and MVID, rare and severe diseases requiring intensive parenteral nutrition (PN) and support, significantly impact the quality of life of both patients and their caregivers," Conte said. "We plan to assess the quality-of-life impact on patients and caregivers as part of both the above-referenced Phase 2 studies."
Conte說:"SBS-IF和MVID是需要強化腸外營養(PN)和支持的罕見重病,嚴重影響患者及其照顧者的生活質量。我們計劃評估患者和照顧者生活質量的影響,作爲上述兩個2期研究的一部分。"
Some SBS patients are subject to intestinal failure, often requiring PN up to seven days a week. Intestinal failure is associated with significant morbidity and mortality; and high medical expenses associated with PN and coincident complications. SBS patients with intestinal failure also have severe chronic diarrhea, and the associated sequelae, including significant dehydration, metabolic acidosis or alkalosis and malnutrition, and other secondary symptoms. These symptoms may emerge at any time, and many times become life-threatening.
一些短腸綜合症患者會出現腸功能衰竭,常常需要每週七天進行腸外營養支持。腸功能衰竭與顯著的發病率和死亡率相關,同時也伴有與腸外營養支持和相關併發症相關的高醫療費用。患有腸功能衰竭的短腸綜合症患者通常還伴有嚴重的慢性腹瀉及相關後遺症,包括嚴重脫水、代謝性酸中毒或鹼中毒和營養不良,及其他次要症狀。這些症狀可能在任何時候出現,並且很多時候會變得危及生命。
As a congenital diarrheal disorder, MVID is more prevalent in cultures with consanguineous marriage customs. Hence, the importance of the company's relationships with health care professionals in the MENA region, which support and are reflected in the recruiting geography of the trials.
作爲一種先天性腹瀉疾病,MVID在有近親結婚習俗的文化中更爲普遍。因此,該公司與醫療保健專業人員在中東和北非地區的關係顯得尤爲重要,這種關係在試驗的招聘地域中得到了支持和體現。
Crofelemer has been granted Orphan Drug Designation by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency for SBS-IF and MVID.
羥基水楊酸已獲得美國食品藥品管理局(FDA)和歐洲藥品管理局的孤兒藥認定,用於短腸綜合症腸功能衰竭和MVID。
About Crofelemer
關於Crofelemer
Crofelemer is a novel, oral plant-based prescription medicine purified from the red bark sap, also referred to as "dragon's blood," of the Croton lechleri tree in the Amazon Rainforest. Napo has established a sustainable harvesting program, under fair trade practices, for crofelemer to ensure a high degree of quality, ecological integrity, and support for indigenous communities.
羥基水楊酸是一種新型的口服植物基處方藥,從亞馬遜雨林中的紅樹皮樹(也稱爲"龍血")的樹汁中提取。Napo已經建立了可持續採收項目,遵循公平交易的規範,以確保羥基水楊酸的高質量、生態完整性和對原住民社區的支持。
About the Jaguar Health Family of Companies
關於Jaguar Health公司家族
Jaguar Health, Inc. (Jaguar) is a commercial stage pharmaceuticals company focused on developing novel proprietary prescription medicines sustainably derived from plants from rainforest areas for people and animals with gastrointestinal distress, specifically associated with overactive bowel, which includes symptoms such as chronic debilitating diarrhea, urgency, bowel incontinence, and cramping pain. Jaguar family company Napo Pharmaceuticals (Napo) focuses on developing and commercializing human prescription pharmaceuticals for essential supportive care and management of neglected gastrointestinal symptoms across multiple complicated disease states. Napo's crofelemer is FDA-approved under the brand name Mytesi for the symptomatic relief of noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy. Jaguar family company Napo Therapeutics is an Italian corporation Jaguar established in Milan, Italy in 2021 focused on expanding crofelemer access in Europe and specifically for orphan and/or rare diseases. Jaguar Animal Health is a Jaguar tradename. Magdalena Biosciences, a joint venture formed by Jaguar and Filament Health Corp. that emerged from Jaguar's Entheogen Therapeutics Initiative (ETI), is focused on developing novel prescription medicines derived from plants for mental health indications.
Jaguar Health, Inc.(Jaguar)是一家商業化階段的製藥公司,專注於開發可持續從雨林地區的植物中提取的新型專有處方藥,用於治療與過度腸道功能相關的人和動物胃腸不適,包括慢性致殘腹瀉,尿急,腸失禁和痙攣性疼痛等症狀。Jaguar旗下的Napo Pharmaceuticals(Napo)專注於爲多個複雜的疾病治療的需要提供人用處方藥的開發和商業化。市場上,Crofelemer通過Mytesi品牌名由FDA批准用於緩解HIV/AIDS患者在抗逆轉錄病毒治療下的艾滋病相關性腹瀉症狀。Jaguar旗下的Napo Therapeutics是一家成立於2021年,總部位於意大利米蘭的意大利公司,專注於擴大Crofelemer在歐洲和特定孤兒和/或罕見疾病中的應用。Jaguar Animal Health是Jaguar的商標名稱。Magdalena Biosciences是Jaguar和Filament Health Corp.組成的合資公司,從Jaguar的靈性治療倡議(ETI)中出現,致力於開發來自植物的新型處方藥用於治療精神健康問題。
For more information about:
更多信息:
Jaguar Health, visit
請訪問jaguar health。
Napo Pharmaceuticals, visit
訪問Napo Pharmaceuticals
Napo Therapeutics, visit napotherapeutics.com
請訪問napotherapeutics.com。
Magdalena Biosciences, visit magdalenabiosciences.com
請訪問magdalenabiosciences.com。
Visit the Make Cancer Less Shitty patient advocacy program on Bluesky, X, Facebook & Instagram
訪問Bluesky的Make Cancer Less Shitty患者倡導計劃,以及X、Facebook和Instagram
Forward-Looking Statements
前瞻性聲明
Certain statements in this press release constitute "forward-looking statements." These include statements regarding Jaguar's expectation that dosing of the first patient in three IITs and two Phase 2 studies of crofelemer will occur throughout December 2024 and Q1 2025, Jaguar's expectation that availability of IIT proof-of-concept results of crofelemer in SBS-IF and/or MVID may potentially occur in Q2 2025, Jaguar's expectation that, in accordance with the guidelines of specific EU countries, published data from clinical investigations could support early patient access to crofelemer for SBS-IF or MVID in these countries, and Jaguar's expectation that it will assess the quality-of-life impact of SBS-IF and/or MVID on patients and caregivers as part of both Phase 2 studies of crofelemer. In some cases, you can identify forward-looking statements by terms such as "may," "will," "should," "expect," "plan," "aim," "anticipate," "could," "intend," "target," "project," "contemplate," "believe," "estimate," "predict," "potential" or "continue" or the negative of these terms or other similar expressions. The forward-looking statements in this release are only predictions. Jaguar has based these forward-looking statements largely on its current expectations and projections about future events. These forward-looking statements speak only as of the date of this release and are subject to several risks, uncertainties, and assumptions, some of which cannot be predicted or quantified and some of which are beyond Jaguar's control. Except as required by applicable law, Jaguar does not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.
本新聞稿中的某些聲明構成「前瞻性聲明」。這些包括關於jaguar health預計在2024年12月以及2025年第一季度,將進行三項IIT和兩項第2階段crofelemer研究的首位患者給藥;jaguar health預計在2025年第二季度可能會出現crofelemer在SBS-IF和/或MVID的IIT概念驗證結果;jaguar health根據特定歐洲國家的指南,預計臨床研究的已發佈數據可以支持這些國家對SBS-IF或MVID的早期患者獲取crofelemer的可能性;以及jaguar health預計將在這兩項第2階段的crofelemer研究中評估SBS-IF和/或MVID對患者和護理人員的生活質量影響。在某些情況下,您可以通過諸如「可能」、「將」、「應該」、「期望」、「計劃」、「目標」、「預期」、「可以」、「打算」、「針對」、「項目」、「考慮」、「相信」、「估計」、「預測」、「潛在」或「繼續」及這些詞的否定形式或其他類似表達來識別前瞻性聲明。本發佈中的前瞻性聲明只是預測。jaguar health主要基於其對未來事件的當前預期和預測來制定這些前瞻性聲明。這些前瞻性聲明僅於本發佈日期時有效,並受到多個風險、不確定性和假設的影響,其中一些是無法預測或量化的,還有一些超出了jaguar health的控制範圍。除適用法律要求外,jaguar health不打算公共更新或修訂本聲明中包含的任何前瞻性聲明,無論是由於任何新信息、未來事件、情況變化或其他原因。
Contact:
聯繫方式:
hello@jaguar.health
Jaguar-JAGX
hello@jaguar.health
Jaguar-JAGX
SOURCE: Jaguar Health, Inc.
資料來源:Jaguar Health, Inc。
譯文內容由第三人軟體翻譯。