Processa Pharmaceuticals to Participate in the EF Hutton Annual Global Conference
Processa Pharmaceuticals to Participate in the EF Hutton Annual Global Conference
HANOVER, Md., May 06, 2024 (GLOBE NEWSWIRE) -- Processa Pharmaceuticals, Inc. (Nasdaq: PCSA) ("Processa" or the "Company"), a clinical-stage pharmaceutical company focused on developing the next generation of chemotherapeutic drugs with improved efficacy and safety, today announced that management will be participating in the EF Hutton Annual Global Conference being held May 15, 2024 at The Plaza Hotel in New York City. Management will be holding one-on-one meetings with investors.
马里兰州汉诺威,2024年5月6日(环球新闻专线)——专注于开发具有更高疗效和安全性的下一代化疗药物的临床阶段制药公司Processa Pharmicals, Inc.(纳斯达克股票代码:PCSA)(“Processa” 或 “公司”)今天宣布,管理层将参加2024年5月15日在纽约广场酒店举行的英孚赫顿年度全球会议。管理层将与投资者举行一对一的会议。
About Processa Pharmaceuticals, Inc.
关于Processa制药公司
Processa is a clinical-stage pharmaceutical company focused on developing the Next Generation Chemotherapy (NGC) drugs to improve the safety and efficacy of cancer treatment. By combining its novel oncology pipeline with proven cancer-killing active molecules and the Processa Regulatory Science Approach, as well as experience in defining Optimal Dosage Regimens for FDA approvals, Processa not only will provide better therapy options to cancer patients, but will also increase the probability of FDA approval for its NGC drugs following an efficient path to approval. Processa's NGC drugs are modifications of existing FDA-approved oncology drugs resulting in an alteration of the metabolism and/or distribution of these drugs while maintaining the existing mechanisms of killing the cancer cells. The Company's approach to drug development is based on more than 30 years of expertise to efficiently design and conduct clinical trials that demonstrate a positive benefit/risk relationship. The Processa team has a track record of obtaining over 30 approvals for indications across almost every division of the FDA. Using its proven Regulatory Science Approach, the Processa Team has experience defining the Optimal Dosage Regimen using the principles of the FDA's Project Optimus Oncology initiative. The advantages of Processa's NGCs are expected to include fewer patients experiencing side effects that lead to dose discontinuation, more significant cancer response and a greater number of patients – in excess of 200,000 for each NGC drug – who will benefit from each NGC drug. Currently under development are three NGC treatments: Next Generation Capecitabine (PCS6422 and capecitabine to treat breast, metastatic colorectal, gastrointestinal, pancreatic and other cancers), Next Generation Gemcitabine (PCS3117 to treat pancreatic, biliary, lung, ovarian, breast and other cancers) and Next Generation Irinotecan (PCS11T to treat lung, colorectal, gastrointestinal, pancreatic and other cancers).
Processa是一家临床阶段的制药公司,专注于开发下一代化疗(NGC)药物,以提高癌症治疗的安全性和有效性。通过将其新型肿瘤学产品线与经过验证的抗癌活性分子和Processa监管科学方法相结合,以及在定义最佳剂量方案以获得FDA批准方面的经验,Processa不仅将为癌症患者提供更好的治疗选择,而且还将增加其NGC药物遵循有效的批准途径获得美国食品药品管理局批准的可能性。Processa的NGC药物是对美国食品药品管理局批准的现有肿瘤药物的修改,导致这些药物的新陈代谢和/或分布发生变化,同时保持杀死癌细胞的现有机制。该公司的药物开发方法基于30多年的专业知识,可以有效地设计和进行临床试验,显示出积极的收益/风险关系。Processa团队有着获得美国食品药品管理局几乎每个部门的30多项适应症批准的记录。利用其成熟的监管科学方法,Processa团队拥有根据美国食品药品管理局Optimus Oncology计划的原则定义最佳剂量方案的经验。预计Processa的NGC的优势将包括减少出现导致停药的副作用的患者,更明显的癌症反应,以及更多将从每种NGC药物中受益的患者(每种NGC药物超过20万人)。目前正在开发三种 NGC 疗法:下一代卡培他滨(PCS6422 和卡培他滨用于治疗乳腺癌、转移性结直肠癌、胃肠道癌、胰腺癌和其他癌症)、下一代吉西他滨(用于治疗胰腺、胆道、肺部、卵巢、乳腺和其他癌症的 PCS3117)和下一代伊立替康(PCS11T 用于治疗肺癌、结直肠癌、胃癌、胰腺癌和其他癌症)乳腺癌和其他癌症)。
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Company Contact:
Patrick Lin
(925) 683-3218
plin@processapharma.com
公司联系人:
帕特里克·林
(925) 683-3218
plin@processapharma.com
Investor Relations Contact:
Yvonne Briggs
LHA Investor Relations
(310) 691-7100
ybriggs@lhai.com
投资者关系联系人:
伊冯娜·布里格斯
LHA 投资者关系
(310) 691-7100
ybriggs@lhai.com
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