Moleculin Biotech, Inc., (Nasdaq: MBRX) (“Moleculin” or the “Company”), a clinical stage pharmaceutical company with a broad portfolio of drug candidates, today announced that it has submitted requests to Polish regulatory authorities for a
HOUSTON, June 4, 2020 /PRNewswire/ -- Moleculin Biotech, Inc., (Nasdaq: MBRX) (“Moleculin” or the “Company”), a clinical stage pharmaceutical company with a broad portfolio of drug candidates, today announced that it has submitted requests to Polish regulatory authorities for approval to open two additional clinical sites for its Phase 1/2 clinical study of Annamycin for the treatment of acute myeloid leukemia (“AML”). “We are pleased to report that the Annamycin trial in AML continues forward despite the disruptions from the COVID-19 pandemic,” commented Walter Klemp, Chairman and CEO of Moleculin. “Two additional hospitals in Poland, one in Szczecin and one in Kielce, have been moving quickly to participate in this trial. Assuming these requests are granted in a timely manner, we expect both sites to begin recruiting in the third quarter.” Moleculin currently has 5 clinical sites for the Annamycin AML clinical trial operating in Europe. The addition of sites in Szczecin and Kielce would bring this total to 7. About Moleculin Biotech, Inc. Moleculin Biotech, Inc. is a clinical stage pharmaceutical company focused on the development of a broad portfolio of oncology drug candidates for the treatment of highly resistant tumors and viruses. The Company’s clinical stage drugs are: Annamycin, a Next Generation Anthracycline, designed to avoid multidrug resistance mechanisms with little to no cardiotoxicity, being studied for the treatment of relapsed or refractory acute myeloid leukemia, more commonly referred to as AML; WP1066, an Immune/Transcription Modulator capable of inhibiting p-STAT3 and other oncogenic transcription factors while also stimulating a natural immune response, being studied for brain tumors, pancreatic cancer and hematologic malignancies; and WP1220, an analog to WP1066, being studied for the topical treatment of cutaneous T-cell lymphoma. Moleculin is also engaged in preclinical development of additional drug candidates, including additional Immune/Transcription Modulators, as well as compounds capable of Metabolism/Glycosylation Inhibition, such as WP1122. For more information about the Company, please visit http://www.moleculin.com. Forward-Looking Statements Contacts
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Company Codes: NASDAQ-SMALL:MBRX |