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Processa Pharmaceuticals Schedules Conference Call to Discuss Third Quarter Results and Provide Drug Development Update on Nov. 12 at 5:30 p.m. ET
HANOVER, Md., Nov. 03, 2020 (GLOBE NEWSWIRE) -- via InvestorWire -- Processa Pharmaceuticals, Inc. (NASDAQ: PCSA) (“Processa” or the “Company”), a

About this update from Processa Pharmaceuticals, Inc.
[{"type":"text","content":"HANOVER, Md., Nov. 03, 2020 (GLOBE NEWSWIRE) -- via InvestorWire -- Processa Pharmaceuticals, Inc. (NASDAQ: PCSA) (“Processa” or the “Company”), a clinical-stage biopharmaceutical company developing products to improve survival and/or quality of life for patients who have high unmet medical need conditions, today announces it will host a conference call and live webcast on Nov. 12, 2020, at 5:30 p.m. Eastern time to discuss its third quarter 2020 results and provide an update on the Company’s clinical pipeline. The update will include a discussion of the Company’s three clinical-stage drugs (each of which addresses potential billion-dollar markets):\n 1) PCS6422 combined with fluoropyrimidines to treat multiple types of cancers. 2) PCS499 to treat ulcerated necrobiosis lipoidica, a rare orphan condition. 3) PCS12852 to treat GI motility conditions such as gastroparesis, the approved drugs and off-label-use drugs for which have caused very serious side effects. Q&A with CEO David Young and the management team will take place at the conclusion of the call. Conference Call Information To participate in this event, dial approximately 5 to 10 minutes before the beginning of the call. Date: Nov. 12, 2020 Time: 5:30 p.m. ET Dial-In Information: Toll Free: 877-876-9176 International: 785-424-1670 Live Webcast: https://www.webcaster4.com/Webcast/Page/2572/38528 Conference Call Replay Information Toll-free: 877-481-4010 International: 919-882-2331 Replay Passcode: 38528 About Processa Pharmaceuticals, Inc. The mission of Processa is to develop products for which existing clinical evidence of efficacy has already been established for unmet or underserved medical conditions for which patients need treatment options that improve survival and or quality of life. The Company used these criteria to develop its pipeline programs in order to effectively and efficiently achieve high-value milestones using the Processa Regulatory Science approach. The members of the Processa development team have been involved with more than 30 drug approvals by the FDA (including drug products targeted to orphan disease conditions) and more than 100 FDA meetings throughout their careers. For more information, visit the company’s website at www.ProcessaPharma.com. Forward-Looking Statements This release contains forward-looking statements. The statements in this pr...