Moleculin Appoints Leading Expert in Pancreatic Cancer to its Scientific Advisory Board to Support Development of Annamycin
Moleculin Biotech (NASDAQ: MBRX) has appointed Dr. Daniel D. Von Hoff to its Annamycin Scientific Advisory Board. Dr. Von Hoff, a Distinguished Professor at the Translational Genomics Research Institute and expert in pancreatic cancer, joins following promising preclinical evidence of Annamycin's potential in treating pancreatic cancer presented at AACR. Annamycin is currently in clinical trials for treating relapsed or refractory acute myeloid leukemia (AML) and soft tissue sarcoma lung metastases. The drug holds Fast Track Status and Orphan Drug Designation from FDA for AML treatment, plus Orphan Drug Designation for soft tissue sarcoma and from EMA for AML.
Moleculin Biotech (NASDAQ: MBRX) ha nominato il Dr. Daniel D. Von Hoff nel suo comitato scientifico consultivo per l'Annamycin. Il Dr. Von Hoff, Professore Distinto presso il Translational Genomics Research Institute ed esperto in cancro pancreatico, si unisce dopo promettenti evidenze precliniche del potenziale dell'Annamycin nel trattamento del cancro pancreatico presentate all'AACR. Annamycin è attualmente in fase di sperimentazione clinica per il trattamento della leucemia mieloide acuta (AML) recidivante o refrattaria e delle metastasi polmonari del sarcoma dei tessuti molli. Il farmaco possiede lo stato di Fast Track e la designazione di Farmaco Orfano da parte della FDA per il trattamento dell'AML, oltre alla designazione di Farmaco Orfano per il sarcoma dei tessuti molli e dalla EMA per l'AML.
Moleculin Biotech (NASDAQ: MBRX) ha nombrado al Dr. Daniel D. Von Hoff en su Consejo Asesor Científico de Annamycin. El Dr. Von Hoff, Profesor Distinguido en el Instituto de Investigación en Genómica Traslacional y experto en cáncer de páncreas, se une tras la prometedora evidencia preclínica del potencial de Annamycin para tratar el cáncer de páncreas presentada en la AACR. Annamycin se encuentra actualmente en ensayos clínicos para el tratamiento de leucemia mieloide aguda (AML) en recaída o refractaria y metástasis en pulmones de sarcoma de tejidos blandos. El fármaco tiene el estatus de Fast Track y Designación de Fármaco Huérfano de la FDA para el tratamiento de la AML, además de Designación de Fármaco Huérfano para sarcoma de tejidos blandos y de la EMA para la AML.
몰레큘린 바이오텍 (NASDAQ: MBRX)는 Annamycin 과학 자문 위원회에 다니엘 D. 본 호프 박사를 임명했습니다. 본 호프 박사는 전이 게놈 연구소의 저명한 교수이자 췌장암 전문가로, AACR에서 췌장암 치료를 위한 Annamycin의 잠재력에 대한 유망한 전임상 증거를 제시한 후 합류했습니다. Annamycin은 현재 재발성 또는 난치성 급성 골수성 백혈병(AML) 및 연조직 육종 폐 전이를 치료하기 위한 임상 시험 중입니다. 이 약물은 AML 치료를 위한 FDA의 Fast Track 상태와 Orphan Drug Designation을 보유하고 있으며, 연조직 육종을 위한 Orphan Drug Designation과 EMA의 AML 인증도 받았습니다.
Moleculin Biotech (NASDAQ: MBRX) a nommé le Dr. Daniel D. Von Hoff dans son Conseil Consultatif Scientifique pour l'Annamycin. Le Dr. Von Hoff, Professeur Distingué au Translational Genomics Research Institute et expert en cancer du pancréas, rejoint l'équipe après des preuves précliniques prometteuses du potentiel de l'Annamycin dans le traitement du cancer du pancréas, présentées à l'AACR. Annamycin est actuellement en essais cliniques pour traiter la leucémie myéloïde aiguë (LMA) en rechute ou réfractaire et les métastases pulmonaires du sarcome des tissus mous. Le médicament bénéficie du statut Fast Track et de la désignation de médicament orphelin de la FDA pour le traitement de la LMA, ainsi que d'une désignation de médicament orphelin pour le sarcome des tissus mous et de l'EMA pour la LMA.
Moleculin Biotech (NASDAQ: MBRX) hat Dr. Daniel D. Von Hoff in sein Wissenschaftlicher Beirat für Annamycin berufen. Dr. Von Hoff, ein herausragender Professor am Translational Genomics Research Institute und Experte für Bauchspeicheldrüsenkrebs, tritt nach vielversprechenden präklinischen Beweisen für das Potenzial von Annamycin zur Behandlung von Bauchspeicheldrüsenkrebs auf der AACR bei. Annamycin befindet sich derzeit in klinischen Studien zur Behandlung von rezidivierter oder refraktärer akuter myeloischer Leukämie (AML) sowie bei Lungenmetastasen des Weichgewebesarkoms. Das Medikament besitzt den Fast Track Status und die Orphan Drug Designation der FDA für AML sowie die Orphan Drug Designation für das Weichgewebesarkom und die EMA für AML.
- Appointment of renowned pancreatic cancer expert Dr. Von Hoff strengthens scientific advisory board
- Promising preclinical evidence for Annamycin in pancreatic cancer treatment
- Multiple FDA designations including Fast Track Status and Orphan Drug Designation
- Ongoing clinical trials in multiple cancer indications (AML and soft tissue sarcoma)
- None.
Strong preclinical evidence of Annamycin's potential for treating pancreatic cancer presented at AACR expands collaboration
Walter Klemp, Chairman and Chief Executive Officer of Moleculin commented, "We are very pleased to welcome Dr. Von Hoff to our Annamycin Scientific Advisory Board (SAB). Although there has been tremendous focus on Annamycin's opportunity in the treatment of AML, there is an even greater unmet need in pancreatic cancer. The organotropic nature of Annamycin and its ability to accumulate at unexpected levels in the pancreas was presented at the Annual Meeting of the AACR and Dr. Von Hoff was among those who recognized the importance of these findings. As a result, he has demonstrated his enthusiasm for Annamycin's potential by agreeing to join our SAB. This is another important reminder that Annamycin has the potential for use in a wide range of cancers."
Daniel D. Von Hoff, M.D., F.A.C.P., FASCO, FAACR
Dr. Von Hoff currently serves as the Distinguished Professor at the Translational Genomics Research Institute (TGen) in
Over the course of his career, Dr. Von Hoff has published more than 790 papers, 143 book chapters and over 1190 abstracts. He is the recipient of the 2010 David A. Karnofsky Memorial Award from the American Society of Clinical Oncology for his outstanding contributions to cancer research leading to significant improvement in patient care and he received the American Association for Cancer Research (AACR) Distinguished Public Service Award in recognition of his extraordinary clinical research career and leadership in establishing the AACR/ASCO Methods in Clinical Cancer Research Workshop to educate and train young clinical investigators. He is also the recipient of the Gold Medal from Columbia University for his outstanding contributions to cancer research leading to significant improvements to patient care.
Dr. Von Hoff was appointed to President Bush's National Cancer Advisory Board in 2004-2010. Dr. Von Hoff is the past President of the AACR, a Fellow of the American College of Physicians, and a member and past board member of the American Society of Clinical Oncology. He is a founder of ILEX™ Oncology, Inc. (acquired by Genzyme after Ilex had 2 agents, alemtuzumab and clofarabine approved by the FDA for patients with leukemia). Dr. Von Hoff is founder and the Editor Emeritus of Investigational New Drugs – The Journal of New Anticancer Agents; and past Editor-in-Chief of Molecular Cancer Therapeutics. He is a co-founder of the AACR/ASCO Methods in Clinical Trial Cancer Research Workshop, which has graduated more than 3,000 clinical trial physicians.
Dr. Von Hoff stated, "I think Annamycin's organotropism and pancreatic data are particularly compelling. I look forward to exploring the breadth of the potential for Annamycin and assisting in the advancement of its development to address areas of significant unmet medical need."
Annamycin is currently being evaluated in ongoing clinical trials for the treatment of relapsed or refractory acute myeloid leukemia (AML) and soft tissue sarcoma (STS) lung metastases. Annamycin currently has Fast Track Status and Orphan Drug Designation from the FDA for the treatment of relapsed or refractory acute myeloid leukemia, in addition to Orphan Drug Designation for the treatment of soft tissue sarcoma. Furthermore, Annamycin has Orphan Drug Designation for the treatment of relapsed or refractory acute myeloid leukemia from the European Medicines Agency (EMA).
About Moleculin Biotech, Inc.
Moleculin Biotech, Inc. is a Phase 3 clinical stage pharmaceutical company advancing a pipeline of therapeutic candidates addressing hard-to-treat tumors and viruses. The Company's lead program, Annamycin, is a next-generation anthracycline designed to avoid multidrug resistance mechanisms and to eliminate the cardiotoxicity common with currently prescribed anthracyclines. Annamycin is currently in development for the treatment of relapsed or refractory acute myeloid leukemia (AML) and soft tissue sarcoma (STS) lung metastases.
The Company is initiating the MIRACLE (Moleculin R/R AML AnnAraC Clinical Evaluation) Trial (MB-108), a pivotal, adaptive design Phase 3 trial evaluating Annamycin in combination with cytarabine, together referred to as AnnAraC, for the treatment of relapsed or refractory acute myeloid leukemia. Following a successful Phase 1B/2 study (MB-106), with input from the FDA, the Company believes it has substantially de-risked the development pathway towards a potential approval for Annamycin for the treatment of AML. This study is subject to appropriate future filings with potential additional feedback from the FDA and their foreign equivalents.
Additionally, the Company is developing WP1066, an Immune/Transcription Modulator capable of inhibiting p-STAT3 and other oncogenic transcription factors while also stimulating a natural immune response, targeting brain tumors, pancreatic and other cancers. Moleculin is also engaged in the development of a portfolio of antimetabolites, including WP1122 for the potential treatment of pathogenic viruses, as well as certain cancer indications.
For more information about the Company, please visit www.moleculin.com and connect on Twitter, LinkedIn and Facebook.
Forward-Looking Statements
Some of the statements in this release are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995, which involve risks and uncertainties. Forward-looking statements in this press release include, without limitation, whether the results shown in the animal models can be replicated in clinical trials. Although Moleculin believes that the expectations reflected in such forward-looking statements are reasonable as of the date made, expectations may prove to have been materially different from the results expressed or implied by such forward-looking statements. Moleculin has attempted to identify forward-looking statements by terminology including 'believes,' 'estimates,' 'anticipates,' 'expects,' 'plans,' 'projects,' 'intends,' 'potential,' 'may,' 'could,' 'might,' 'will,' 'should,' 'approximately' or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. These statements are only predictions and involve known and unknown risks, uncertainties, and other factors, including those discussed under Item 1A. "Risk Factors" in our most recently filed Form 10-K filed with the Securities and Exchange Commission ("SEC") and updated from time to time in our Form 10-Q filings and in our other public filings with the SEC. Any forward-looking statements contained in this release speak only as of its date. We undertake no obligation to update any forward-looking statements contained in this release to reflect events or circumstances occurring after its date or to reflect the occurrence of unanticipated events.
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SOURCE Moleculin Biotech, Inc.
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