BRC-002 Receives Orphan Drug Designation From FDA for Complex Regional Pain Syndrome
BRC-002 Receives Orphan Drug Designation From FDA for Complex Regional Pain Syndrome
- Safety and efficacy are currently being assessed in investigator-initiated clinical trial.
- BRC is planning to commence enrollment for a Phase 2 trial by the end of 2025.
- 目前正在评估安全性和有效性,这是由调查员发起的临床试验。
- BRC计划在2025年底开始进行第2期试验的招募。
MONTEREY, Calif., Dec. 3, 2024 /PRNewswire/ -- Biopharmaceutical Research Company (BRC), a specialty pharmaceutical company developing proprietary cannabinoid therapeutics, announced today that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation for the treatment of Complex Regional Pain Syndrome (CRPS) to BRC-002, which is being investigated in an investigator-initiated clinical Phase 1 trial. Visit for more information.
加州蒙特雷,2024年12月3日 / 美通社 / - 生物制药研究公司(BRC)是一家专业的药品公司,开发专有的大麻素治疗药物。今天宣布,美国食品药品监督管理局(FDA)已授予BRC治疗复杂性区域性疼痛综合征(CRPS)的孤儿药物认定,针对正在调查中的BRC-002,该药正在进行由调查员发起的临床一期试验。访问 获取更多信息。
CRPS is a debilitating chronic pain condition that is often triggered by an injury, such as a fracture or surgery. In addition to severe pain, patients can suffer from co-morbidities such as depression, anxiety, and sleep disorders. BRC-002 is a novel, botanically derived oral cannabinoid therapeutic product candidate aiming to address pain and co-morbidities of CRPS. BRC's cannabinoid therapeutics contain major and minor cannabinoids at defined and proprietary ratios.
CRPS是一种严重影响生活质量的慢性疼痛病症,经常由受伤引发,如骨折或手术。除了剧痛外,患者还可能患有抑郁症、焦虑症和睡眠障碍等共病。BRC-002是一种新型、植物源口服大麻素治疗产品候选药,旨在应对CRPS的疼痛和共病。BRC的大麻素治疗药物含有主要和次要大麻素,按照确定的专有比例配制。
"The Orphan Drug Designation for BRC-002 reinforces the urgency to identify safe and effective treatment options for patients afflicted with CRPS" said George Hodgin, CEO and founder of BRC. "The designation represents another milestone in our efforts to provide a holistic solution for these patients by addressing pain and improving overall quality of life. We look forward to progressing this investigational treatment and sharing updates in the near future."
BRC的创始人兼首席执行官乔治·霍金表示:“BRC-002的孤儿药物认定加强了我们识别针对CRPS患者安全有效治疗选择的迫切性。” “这一认定代表着我们为这些患者提供全面解决方案的努力中的又一个里程碑,通过应对疼痛和改善整体生活质量。我们期待推进这项研究性治疗,并在不久的将来分享更新。”
Currently, there is no approved treatment for CRPS in the United States, highlighting the critical need for new therapeutic approaches for this underserved disease. BRC is planning to commence enrollment for a Phase 2 trial by the end of 2025 and is currently seeking input from the FDA on the development plan.
目前,美国尚无批准用于CRPS的治疗方法,突显了对这种待办病症新治疗方法的迫切需求。BRC计划于2025年底开始进行第2期试验的招募,目前正在与FDA就开发计划征求意见。
The FDA grants Orphan Drug Designation to a drug intended to treat, prevent, or diagnose a rare disease or condition that affects fewer than 200,000 people in the US at the time of designation. The designation provides incentives, such as tax credits for qualified clinical trials, user fee exemptions, and the potential of seven years of market exclusivity after approval.
FDA对旨在治疗、预防或诊断罕见疾病或条件的药物授予孤儿药物认定。在认定时,该疾病在美国影响的人数不超过20万。该认定提供激励措施,如对符合条件的临床试验享受税收抵免、用户费用豁免,并在获批后可能获得七年的市场独占权。
About Biopharmaceutical Research Company (BRC)
Biopharmaceutical Research Company (BRC) is a specialty pharmaceutical company focused on developing proprietary cannabinoid therapeutics to address high unmet medical needs. BRC's therapeutics are polymodal and contain major and minor cannabinoids at defined ratios. BRC has developed a pipeline of treatments addressing pain and neurological and inflammatory conditions. BRC is registered with the Drug Enforcement Administration and is based in Monterey, CA.
关于生物制药研究公司(BRC)
生物制药研究公司(BRC)是一家专注于开发专有大麻素治疗药物的专业药品公司,以解决高度未满足的医疗需求。BRC的治疗药物是多模式的,并含有特定比例的主要和次要大麻素。BRC已经开发了一系列治疗方案,涉及疼痛、神经和炎症等病症。BRC已在蒙特雷,加州注册,并获得了药品执法管理局的注册。
To learn more about BRC, visit .
要了解更多关于BRC的信息,请访问 。
Forward-Looking Statements
前瞻性声明
This news release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 that involve risks, uncertainties and assumptions, including without limitation statements about the development, use, benefits and effects of Biopharmaceutical Research Company's (BRC) therapeutic product candidate and related technology, future plans for the BRC's business and growth, expected plans with respect to clinical trials, including the number of patients enrolled and timing of patient enrollment. In some cases, you can identify forward-looking statements by terms such as "may," "will," "should," "expect," "design," "plan," "anticipate," "could," "intend," "target," "project," "contemplates," "believes," "estimates," "predicts," "potential" or "continue" or the negative of these terms or other similar expressions. Such statements and other statements in this press release that are not descriptions of historical facts are forward-looking statements that are based on management's current expectations and assumptions and are subject to risks and uncertainties. If such risks or uncertainties materialize or such assumptions prove incorrect, our business, operating results, financial condition, and stock price could be materially negatively affected. Actual results and the timing of events could differ materially from those anticipated in these forward-looking statements. The forward-looking statements made herein speak only as of the date of this press release and, unless otherwise required by law, BRC does not undertake any obligation to publicly update such forward-looking statements to reflect subsequent events or circumstances.
这则新闻稿包含根据1933年证券法第27(A)条和1934年证券交易法第21(E)条含有风险、不确定性和假设的前瞻性声明,包括但不限于生物制药研究公司(BRC)治疗产品候选药的开发、用途、益处和效果,以及相关技术,BRC业务和增长的未来计划,临床试验方面的预期计划,包括入组患者数量和入组时间。在某些情况下,通过诸如“可能”、“将”、“应”、“期望”、“设计”、“计划”、“预期”、“可能”、“打算”、“目标”、“项目”、“考虑”、“相信”、“估计”、“预测”、“潜在”或“继续”等术语可识别前瞻性声明。这些声明及本新闻稿中非历史事实的其他声明都是基于管理层的当前期望和假设,并且受到风险和不确定性的影响。如果这些风险或不确定性变为现实,或这些假设证明不准确,我们的业务、运营结果、财务状况和股价可能受到严重的负面影响。实际结果和事件的时间可能与这些前瞻性声明中预期的情况有重大不同。本处的前瞻性声明仅适用于此新闻稿的发布日期,并且除非法律另有要求,BRC不承担任何义务来公开更新此类前瞻性声明以反映随后发生的事件或情况。
SOURCE Biopharmaceutical Research Company
SOURCE生物医药研究公司