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Relief Therapeutics Enters Into Exclusive U.S. License and Supply Agreement With Eton Pharmaceuticals for PKU GOLIKE

Relief Therapeutics Enters Into Exclusive U.S. License and Supply Agreement With Eton Pharmaceuticals for PKU GOLIKE

Relief Therapeutics与伊顿制药就PKU GOLIKE签订美国独家许可和供应协议
Accesswire ·  03/22 02:20

GENEVA, SWITZERLAND / ACCESSWIRE / March 22, 2024 / RELIEF THERAPEUTICS Holding SA (SIX:RLF)(OTCQB:RLFTF)(OTCQB:RLFTY ) (Relief, or the Company), a biopharmaceutical company committed to delivering innovative treatment options for select specialty, unmet and rare diseases, today announced it has granted an exclusive license to Eton Pharmaceuticals, Inc. (Nasdaq: ETON) (Eton) for the commercialization of GOLIKE family of products in the United States.

瑞士日内瓦/ACCESSWIRE /2024年3月22日/致力于为特定特种疾病、未满足的和罕见疾病提供创新治疗选择的生物制药公司RELIEF THERAPEUTICS Holding SA(SIX: RLFTF)(OTCQB: RLFTY)(OTCQB: RLFTY)(Relief,或公司)今天宣布,已向伊顿制药公司(ETON Nasdaq)(Eton Nasdaq)(伊顿公学)(Eton)授予独家许可用于 GOLIKE 的商业化 美国的产品系列。

"This transition is fully aligned with Relief's strategy of moving the GOLIKE products into partnership models in the U.S. and Europe. We are very pleased to be establishing this partnership with Eton for GOLIKE patients in the U.S. given their valuable experience in the metabolic area," said Michelle Lock, interim CEO of Relief.

“这种过渡完全符合Relief的战略,即在美国和欧洲将GOLIKE产品转变为合作伙伴模式。鉴于美国GOLIKE患者在新陈代谢领域的宝贵经验,我们很高兴与伊顿建立这种合作伙伴关系。” Relief临时首席执行官米歇尔·洛克说。

"We are excited to be partnering with Relief on PKU GOLIKE in the United States. After extensive discussions with metabolic geneticists, dieticians, and PKU patients, we believe PKU GOLIKE is the best product in the estimated $100 million U.S. PKU medical formula market. With our sales force and existing relationships in the metabolic community, we believe we can significantly increase the awareness, education, and adoption of this important product," said Sean Brynjelsen, CEO of Eton Pharmaceuticals.

“我们很高兴能与救济组织合作开发美国的PKU GOLIKE。在与代谢遗传学家、营养师和PKU患者进行了广泛讨论后,我们认为PKU GOLIKE是估计耗资1亿美元的美国PKU医疗配方市场中最好的产品。凭借我们的销售队伍和代谢界的现有关系,我们相信我们可以显著提高对这一重要产品的认识、教育和采用率。” 伊顿制药首席执行官肖恩·布林杰尔森说。

Under the terms of the agreement, Relief will receive an upfront payment of $2.2 million and is eligible to receive an additional $2.0 million in sales milestones payments as well as mid-teens royalties on net sales. In the fourth quarter of 2023, PKU GOLIKE's annualized net sales exceeded $1 million in the U.S., continuing its growth trajectory since its launch in late 2022.

根据协议条款,Relief将获得220万美元的预付款,并有资格额外获得200万美元的销售里程碑款项以及十几岁的净销售特许权使用费。2023年第四季度,北京大学GOLIKE在美国的年化净销售额超过100万美元,延续了自2022年底推出以来的增长轨迹。

As part of the agreement, Eton also received U.S. rights to Relief's GOLIKE Medical Food line extensions under development for the management of other inherited rare metabolic diseases such as tyrosinemia and homocystinuria, which are both expected to launch in 2025 and 2026 under the same trademark. Relief is also in discussions with Eton related to additional development assets, including RLF-OD032. RLF‐OD032 is an innovative drug product candidate under development for the treatment of PKU expected to be filed for approval before the FDA in H2/2025 as 505(b)(2) application. Relief will continue to fully own GOLIKE rights outside the United States.

作为协议的一部分,伊顿还获得了美国救济基金GOLIKE Medical Food系列延期的权利,该产品线用于管理酪氨酸血症和高半胱氨酸尿症等其他遗传性罕见代谢疾病,这些疾病预计都将在2025年和2026年以同一商标推出。还正在与伊顿公学就包括 RLF-OD032 在内的其他开发资产进行救济讨论。RLF‐OD032是一种正在开发的用于治疗PKU的创新候选药物,预计将于2025年下半年作为505(b)(2)申请向美国食品药品管理局申请批准。救济将继续完全拥有GOLIKE在美国以外的版权。

About Relief

关于救济

Relief is a commercial-stage biopharmaceutical company committed to advancing treatment paradigms and delivering improvements in efficacy, safety, and convenience to benefit the lives of patients living with select specialty and rare diseases. Relief's portfolio offers a balanced mix of marketed, revenue-generating products, our proprietary, globally patented Physiomimic and TEHCLO platform technologies and a targeted clinical development pipeline consisting of risk-mitigated assets focused in three core therapeutic areas: rare metabolic disorders, rare skin diseases and rare respiratory diseases. In addition, Relief is commercializing several legacy products via licensing and distribution partners. Relief's mission is to provide therapeutic relief to those suffering from rare diseases and is being advanced by an international team of well-established, experienced biopharma industry leaders with extensive research, development and rare disease expertise. Relief is headquartered in Geneva, with additional offices in Balerna, Switzerland, Offenbach am Main, Germany and Monza, Italy. Relief is listed on the SIX Swiss Exchange under the symbol RLF and quoted in the U.S. on OTCQB under the symbols RLFTF and RLFTY. For more information, please visit our website or follow Relief on LinkedIn.

Relief 是一家处于商业阶段的生物制药公司,致力于推进治疗模式,改善疗效、安全性和便利性,以造福特定特种和罕见疾病患者的生活。Reliev的产品组合平衡地组合了已上市的创收产品、我们在全球获得专利的Physiomic和TEHCLO平台技术,以及由风险缓解资产组成的有针对性的临床开发管线,这些资产侧重于三个核心治疗领域:罕见代谢疾病、罕见皮肤病和罕见呼吸道疾病。此外,Relief正在通过许可和分销合作伙伴将几种传统产品商业化。Relief的使命是为罕见疾病患者提供治疗性救济,由一支由知名的、经验丰富的生物制药行业领导者组成的具有广泛研究、开发和罕见病专业知识的国际团队正在推动这一使命。Relief总部设在日内瓦,在瑞士巴莱尔纳、德国美因河畔奥芬巴赫和意大利蒙扎设有办事处。救济在瑞士证券交易所上市,股票代码为RLF,并在美国的OTCQB上市,股票代码为RLFTF和RLFTY。欲了解更多信息,请访问我们的网站或在 LinkedIn 上关注 Relief。

About Eton Pharmaceuticals

关于伊顿制药

Eton is an innovative pharmaceutical company focused on developing and commercializing treatments for rare diseases. It currently has five commercial rare disease products: ALKINDI SPRINKLE , PKU GOLIKE , Carglumic Acid, Betaine Anhydrous, and Nitisinone. Eton has three additional product candidates in late-stage development: ET-400, ET-600, and ZENEO hydrocortisone autoinjector. For more information, visit .

伊顿是一家创新制药公司,专注于开发和商业化罕见疾病的治疗方法。它目前有五种商业罕见病产品:ALKINDI SPRINKLE ,PKU GOLIKE 、葡萄糖酸、无水甜菜碱和尼替西农。伊顿还有三款处于后期开发阶段的候选产品:ET-400、ET-600 和 ZENEO 氢化可的松自动注射器。欲了解更多信息,请访问。

About Phenylketonuria (PKU)

关于苯丙酮尿症(PKU)

Phenylketonuria (PKU) is caused by a defect of the enzyme needed to break down phenylalanine (Phe), leading to a toxic buildup of Phe from the consumption of foods containing protein or aspartame. Untreated PKU can result in global developmental delay or severe irreversible intellectual disability, as well as growth failure, hypopigmentation, motor deficits, ataxia and seizures. Living with PKU requires a limited diet and very careful management. If left unmanaged, PKU can lead to devastating consequences, such as brain damage. People living with PKU do not have the ability to metabolize Phe, which is found in many foods, and they require supplementation of amino acid-based phenylalanine-free Medical Foods to prevent protein deficiency and optimize metabolic control. Currently available Medical Foods may lead to poor or suboptimal clinical outcomes and compliance because they are rapidly absorbed and are characterized by an unpleasant odor and aftertaste. Such factors contribute to barriers to social interaction for PKU patients, further limiting Medical Foods compliance and exposing patients to the risks of poor disease control.

苯丙酮尿症(PKU)是由分解苯丙氨酸(Phe)所需的酶缺陷引起的,食用含有蛋白质或阿斯巴甜的食物会导致Phe的毒性积聚。未经治疗的PKU可能导致全球发育迟缓或严重的不可逆的智力障碍,以及生长衰竭、色素减退、运动缺陷、共济失调和癫痫发作。与PKU一起生活需要有限的饮食和非常谨慎的管理。如果不加以管理,PKU可能导致毁灭性的后果,例如脑损伤。PKU患者没有能力代谢PHE,PHE存在于许多食物中,他们需要补充基于氨基酸的无苯丙氨酸医疗食品,以防止蛋白质缺乏和优化代谢控制。目前可用的医疗食品可能会导致较差或次优的临床结果和依从性,因为它们会被迅速吸收,并且具有难闻的气味和回味。这些因素构成了PKU患者的社交互动障碍,进一步限制了医疗食品的依从性,使患者面临疾病控制不佳的风险。

About PKU GOLIKE

关于 PKU GOLIKE

PKU GOLIKE products are Medical Foods for the dietary management of PKU in both children and adults. Developed with the Relief proprietary, patent-protected Physiomimic Technology drug delivery platform, PKU GOLIKE products are the first prolonged-release amino acid Medical Food, characterized by a special coating that ensures physiological absorption of the amino acids mirroring that of natural proteins. The special coating also masks the unpleasant taste, odor and aftertaste of the amino acids. PKU GOLIKE granules are flavorless and can be mixed with many foods. PKU GOLIKE granule products contain all 19 amino acids that people with PKU need to maintain neurological and muscular health and is fortified with vitamins and minerals, including ones normally found in protein-rich foods like iron, calcium, and vitamin B12. The PKU GOLIKE line of products is available in convenient packets (PKU GOLIKE Plus 3-16 and 16+) and medical food bars (PKU GOLIKE BAR ). PKU GOLIKE products have been commercially available in the U.S. since October 2022. For more information, visit (this site is intended for U.S. audiences only).

PKU GOLIKE 产品是用于儿童和成人 PKU 膳食管理的医疗食品。采用 Relief 专有的、受专利保护的 Physiomic Technology 药物递送平台 PKU GOLIKE 开发 产品是第一款长释氨基酸医用食品,其特点是特殊涂层可确保氨基酸的生理吸收,与天然蛋白质类似。特殊涂层还掩盖了氨基酸的难闻味道、气味和回味。PKU GOLIKE 颗粒无味,可以与许多食物混合。PKU GOLIKE 颗粒产品含有PKU患者维持神经和肌肉健康所需的全部19种氨基酸,并富含维生素和矿物质,包括通常存在于铁、钙和维生素B12等富含蛋白质的食物中的维生素和矿物质。PKU GOLIKE 产品系列有方便的包装可供选择(PKU GOLIKE Plus) 3-16 和 16 岁以上)和医疗食品棒(PKU GOLIKE BAR) )。PKU GOLIKE 自2022年10月以来,产品已在美国上市。欲了解更多信息,请访问(本网站仅供美国受众使用)。

CONTACT :

联系 :

RELIEF THERAPEUTICS Holding SA
Avenue de Sécheron 15
1202 Geneva
Switzerland
contact@relieftherapeutics.com

救济疗法控股有限公司
塞切隆大道 15
1202 日内瓦
瑞士
contact@relieftherapeutics.com

DISCLAIMER

免责声明

This press release contains forward-looking statements. Forward-looking statements involve known and unknown risks, uncertainties, including its ability to achieve its corporate, development and commercial goals, and other factors which could cause the actual results, financial condition, performance or achievements of Relief to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. A number of factors, including those described in Relief's filings with the SIX Swiss Exchange and the U.S. Securities and Exchange Commission (SEC), could adversely affect Relief. Copies of Relief's filings with the SEC are available on the SEC EDGAR database at www.sec.gov. Relief does not undertake any obligation to update the information contained herein, which speaks only as of this date.

本新闻稿包含前瞻性陈述。前瞻性陈述涉及已知和未知的风险、不确定性,包括其实现公司、发展和商业目标的能力,以及其他可能导致救济基金的实际业绩、财务状况、业绩或成就与此类前瞻性陈述所表达或暗示的任何未来业绩、业绩或成就存在重大差异的因素。许多因素,包括救济基金向瑞士证券交易所和美国证券交易委员会(SEC)提交的文件中描述的因素,可能会对救济产生不利影响。救济组织向美国证券交易委员会提交的文件副本可在美国证券交易委员会EDGAR数据库www.sec.gov上查阅。Relief不承担任何义务更新此处包含的信息,这些信息仅涉及截至该日期。

SOURCE: Relief Therapeutics Holdings AG

资料来源:救济疗控股股份公司


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