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.
馬里蘭州漢諾威,2024年5月6日(環球新聞專線)——專注於開發具有更高療效和安全性的下一代化療藥物的臨床階段製藥公司Processa Pharmicals, Inc.(納斯達克股票代碼:PCSA)(“Processa” 或 “公司”)今天宣佈,管理層將參加2024年5月15日在紐約廣場酒店舉行的英孚赫頓年度全球會議。管理層將與投資者舉行一對一的會議。
About Processa Pharmaceuticals, Inc.
關於Processa製藥公司
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是一家臨床階段的製藥公司,專注於開發下一代化療(NGC)藥物,以提高癌症治療的安全性和有效性。通過將其新型腫瘤學產品線與經過驗證的抗癌活性分子和Processa監管科學方法相結合,以及在定義最佳劑量方案以獲得FDA批准方面的經驗,Processa不僅將爲癌症患者提供更好的治療選擇,而且還將增加其NGC藥物遵循有效的批准途徑獲得美國食品藥品管理局批准的可能性。Processa的NGC藥物是對美國食品藥品管理局批准的現有腫瘤藥物的修改,導致這些藥物的新陳代謝和/或分佈發生變化,同時保持殺死癌細胞的現有機制。該公司的藥物開發方法基於30多年的專業知識,可以有效地設計和進行臨床試驗,顯示出積極的收益/風險關係。Processa團隊有着獲得美國食品藥品管理局幾乎每個部門的30多項適應症批准的記錄。利用其成熟的監管科學方法,Processa團隊擁有根據美國食品藥品管理局Optimus Oncology計劃的原則定義最佳劑量方案的經驗。預計Processa的NGC的優勢將包括減少出現導致停藥的副作用的患者,更明顯的癌症反應,以及更多將從每種NGC藥物中受益的患者(每種NGC藥物超過20萬人)。目前正在開發三種 NGC 療法:下一代卡培他濱(PCS6422 和卡培他濱用於治療乳腺癌、轉移性結直腸癌、胃腸道癌、胰腺癌和其他癌症)、下一代吉西他濱(用於治療胰腺、膽道、肺部、卵巢、乳腺和其他癌症的 PCS3117)和下一代伊立替康(PCS11T 用於治療肺癌、結直腸癌、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
公司聯繫人:
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
投資者關係聯繫人:
伊馮娜·布里格斯
LHA 投資者關係
(310) 691-7100
ybriggs@lhai.com
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