Previous Close | 0.4514 |
Open | 0.4700 |
Bid | 0.4403 x 900 |
Ask | 0.4490 x 800 |
Day's Range | 0.4001 - 0.4725 |
52 Week Range | 0.3850 - 4.0100 |
Volume | |
Avg. Volume | 295,993 |
Market Cap | 10.524M |
Beta (5Y Monthly) | 0.06 |
PE Ratio (TTM) | N/A |
EPS (TTM) | -1.0000 |
Earnings Date | Mar 28, 2023 - Apr 03, 2023 |
Forward Dividend & Yield | N/A (N/A) |
Ex-Dividend Date | N/A |
1y Target Est | 6.33 |
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The 300 mg dose group will provide more information on the drug exposure vs adverse event relationship which is critical to FDA approval given the FDA’s Project Optimus Oncology initiative.Patients treated with Next Generation Chemotherapy-Capecitabine have NOT had hand-foot syndrome or cardiotoxicity adverse events, typically seen in 50-70% of patients presently on FDA-approved capecitabine.In mid-April Processa expects guidance from FDA on our Phase 2B trial design and our Project Optimus appr
HANOVER, MD, March 07, 2023 (GLOBE NEWSWIRE) -- Processa Pharmaceuticals, Inc. (Nasdaq: PCSA) (“Processa” or the “Company”), the developer of the Next Generation Chemotherapy drugs that will provide a better safety-efficacy profile than their widely used FDA-approved counterparts, today announced that the Company’s President & CEO, Dr. David Young, will present virtually at the Oppenheimer 33rd Annual Healthcare Conference on March 14, 2023 at 12:00 PM Eastern. The company is looking forward to
Our Next Generation Chemotherapies (NGCs) are cancer treatments where the metabolism and/or distribution of an FDA-approved drug has been altered to provide potentially safer and more effective chemotherapy to cancer patients.Based on preliminary clinical and pre-clinical studies, more cancer patients should benefit from our NGCs than their FDA-approved counterpart drugs.Our Regulatory Science approach, encompassing the principles of FDA’s Project Optimus and Oncology Guidance, should increase t