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Relief Therapeutics Completes Clinical Phase in RLF-OD032 Proof-of-Concept Study; Topline Results Expected in October 2024

Relief Therapeutics Completes Clinical Phase in RLF-OD032 Proof-of-Concept Study; Topline Results Expected in October 2024

Relief Therapeutics完成RLF-OD032概念验证研究的临床阶段;预计于2024年10月发布首要结果。
Accesswire ·  2024/09/18 13:20

GENEVA, SWITZERLAND / ACCESSWIRE / September 18, 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 that it has completed dosing in its proof-of-concept clinical study of RLF-OD032 for the treatment of phenylketonuria (PKU), a rare inherited disorder affecting phenylalanine metabolism.

瑞士日内瓦/ ACCESSWIRE / 2024年9月18日 / 缓解治疗控股公司(SIX:RLF)(OTCQB:RLFTF)(OTCQB:RLFTY)(下称缓解,或公司)是一家专注于为特定专业、未满足和罕见疾病提供创新治疗选择的生物制药公司。今天宣布,它已完成了用于苯丙酮尿症(PKU)治疗的RLF-OD032概念验证临床研究的给药。PKU是一种罕见的遗传性疾病,影响苯丙氨酸代谢。

The primary objectives of the study include the comparison of RLF-OD032 to a currently marketed sapropterin dihydrochloride product, with a focus on bioavailability under fed and fasting conditions. The Company expects topline results in October 2024. These results will inform further development of RLF-OD032 toward a pivotal trial and potential regulatory submission under the 505(b)(2) NDA pathway in the United States.

该研究的主要目标包括将RLF-OD032与目前市场销售的羟异丙酮二盐酸盐产品进行比较,重点关注饮食和禁食条件下的生物利用度。公司预计将在2024年10月公布首要结果。这些结果将为RLF-OD032的进一步开发提供信息,以备进行至关重要的试验和在美国进行可能的505(b)(2) NDA路径下的监管提交。

RLF-OD032, an innovative and highly concentrated liquid formulation of sapropterin dihydrochloride, is designed to lower blood phenylalanine in adult and pediatric PKU patients. It offers a more patient-friendly solution by significantly reducing the volume of medication required compared to current formulations. This advancement aims to enhance compliance, particularly among pediatric patients, who often struggle with the high volumes associated with existing sapropterin treatments. If approved, RLF-OD032 would be the first and only portable, ready-to-use liquid formulation of sapropterin dihydrochloride.

RLF-OD032是羟异丙酮二盐酸盐的一种创新和高浓度液体制剂,旨在降低成人和儿童PKU患者的血液苯丙氨酸含量。与当前的制剂相比,它能够显著减少所需药物的用量,为患者提供更方便的解决方案。这一进展旨在提高依从性,特别是在儿童患者中,他们往往难以应对现有羟异丙酮治疗的大量用量。如果获批,RLF-OD032将成为第一款也是唯一一款便携式、即用型的羟异丙酮二盐酸盐液体制剂。

ABOUT RELIEF
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, proprietary, globally patented TEHCLO and Physiomimic platform technologies and a targeted clinical development pipeline consisting of risk-mitigated assets focused in three core therapeutic areas: rare skin diseases, rare metabolic disorders, and rare respiratory diseases. In addition, Relief is commercializing several legacy products via licensing and distribution partners. Headquartered in Geneva, 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, visit .

关于救济
Relief是一家商业化阶段的生物制药公司,致力于推进治疗范式,提高治疗效果,安全性和便利性,从而造福于患有特定专业和罕见疾病的患者。 Relief的组合产品提供了平衡的市场,产生收入,专有,全球专利TEHCLO和Physiomimic平台技术以及定向临床开发管道,包括三个核心治疗领域:罕见的皮肤病,罕见的代谢性疾病和罕见的呼吸道疾病。此外,Relief通过授权和分销合作伙伴商业化了数种传统产品。 总部设在日内瓦,Relief在SIX Swiss Exchange上市,代码为RLF,在OTCQb上引用代码为RLFTF和RLFTY。 有关更多信息,访问。

CONTACT :
RELIEF THERAPEUTICS Holding SA
Jeremy Meinen
Chief Financial Officer
contact@relieftherapeutics.com

联系方式 :
RELIEF THERAPEUTICS Holding SA
Jeremy Meinen
致富金融(临时代码)官
contact@relieftherapeutics.com

DISCLAIMER
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.

免责声明
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,包括其实现其公司,开发和商业目标的能力,以及可能导致Relief的实际结果,财务状况,绩效或成就与任何未来结果,绩效或预期的前瞻性陈述有实质不同的因素。诸如上述因素的数量,在Relief与美国证券交易委员会(SEC)的SIX Swiss Exchange和SEC的文件中描述,可能会对Relief产生不利影响。 Relief的文件备份可在SEC EDGAR数据库中查询www.sec.gov。 Relief不承担更新此处所含信息的任何义务,该信息仅于本日期有效。

SOURCE: Relief Therapeutics Holdings AG

SOURCE:Relief Therapeutics Holdings AG


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