Moleculin to Host Virtual Acute Myeloid Leukemia KOL Event on October 14, 2024
Moleculin Biotech, Inc. (Nasdaq: MBRX) has announced a Virtual Acute Myeloid Leukemia (AML) KOL event scheduled for October 14, 2024, from 11:00 AM to 1:00 PM ET. The event will feature discussions on Annamycin, the company's drug candidate for treating relapsed or refractory AML, and its ongoing pivotal Phase 3 clinical trial (the 'MIRACLE' trial).
Key participants include Moleculin's management team and renowned AML experts from prestigious institutions. The event will cover topics such as the use of anthracyclines, Annamycin's potential impact on AML treatment, and details about the global Phase 3 trial. Interested parties can join via conference call or watch the live video webcast on Moleculin's website.
Moleculin Biotech, Inc. (Nasdaq: MBRX) ha annunciato un evento KOL virtuale dedicato alla Leucemia Mieloide Acuta (AML) programmato per il 14 ottobre 2024, dalle 11:00 alle 13:00 ET. L'evento includerà discussioni su Annamycin, il candidato farmaco dell'azienda per il trattamento dell'AML in recidiva o refrattaria, e il suo attuale trial clinico cruciale di Fase 3 (il trial 'MIRACLE').
I partecipanti chiave includeranno il team di gestione di Moleculin e rinomati esperti di AML provenienti da istituzioni prestigiose. L'evento tratterà argomenti come l'uso degli antibiotici, l'impatto potenziale di Annamycin sul trattamento dell'AML e dettagli sul trial globale di Fase 3. Le parti interessate possono partecipare tramite teleconferenza o guardare la diretta video sul sito web di Moleculin.
Moleculin Biotech, Inc. (Nasdaq: MBRX) ha anunciado un evento KOL virtual sobre Leucemia Mieloide Aguda (AML) programado para el 14 de octubre de 2024, de 11:00 AM a 1:00 PM ET. El evento contará con discusiones sobre Annamycin, el candidato a medicamento de la empresa para tratar AML en recaída o refractaria, y su trial clínico pivotal de Fase 3 en curso (el trial 'MIRACLE').
Los participantes clave incluirán al equipo de gestión de Moleculin y a renombrados expertos en AML de instituciones prestigiosas. El evento abordará temas como el uso de antraciclinas, el impacto potencial de Annamycin en el tratamiento de AML y detalles sobre el trial global de Fase 3. Las partes interesadas pueden unirse a través de una llamada conferencia o ver la transmisión web en vivo en el sitio web de Moleculin.
Moleculin Biotech, Inc. (Nasdaq: MBRX)는 2024년 10월 14일 오후 11시부터 1시(ET)까지 예정된 가상 급성 골수성 백혈병(AML) KOL 이벤트를 발표했습니다. 이 이벤트에서는 재발 또는 불응성 AML 치료를 위한 회사의 약물 후보인 Annamycin과 현재 진행 중인 주요 3상 임상 시험('MIRACLE' 시험)에 대한 논의가 포함됩니다.
주요 참가자에는 Moleculin의 경영진 팀과 명망 있는 기관의 AML 전문가들이 포함됩니다. 이 이벤트는 항암제의 사용, AML 치료에 대한 Annamycin의 잠재적 영향 및 글로벌 3상 시험에 대한 세부 사항과 같은 주제를 다룰 것입니다. 관심 있는 분들은 전화 회의에 참여하거나 Moleculin 웹사이트에서 라이브 비디오 웹캐스트를 시청할 수 있습니다.
Moleculin Biotech, Inc. (Nasdaq: MBRX) a annoncé un événement KOL virtuel sur la leucémie myéloïde aiguë (AML) prévu pour le 14 octobre 2024, de 11h00 à 13h00 ET. L'événement comprendra des discussions sur Annamycin, le candidat médicament de l'entreprise pour le traitement de l'AML en rechute ou réfractaire, et son essai clinique pivot de phase 3 en cours (l'essai 'MIRACLE').
Les participants clés incluront l'équipe de direction de Moleculin et des experts renommés de l'AML provenant d'institutions prestigieuses. L'événement couvrira des sujets tels que l'utilisation des anthracyclines, l'impact potentiel d'Annamycin sur le traitement de l'AML, et des détails sur l'essai mondial de phase 3. Les parties intéressées peuvent participer via conférence téléphonique ou regarder la diffusion vidéo en direct sur le site web de Moleculin.
Moleculin Biotech, Inc. (Nasdaq: MBRX) hat ein virtuelles KOL-Event zur akuten myeloischen Leukämie (AML) angekündigt, das für den 14. Oktober 2024, von 11:00 bis 13:00 Uhr ET geplant ist. Bei der Veranstaltung werden Diskussionen über Annamycin, das Medikamentenkandidat des Unternehmens zur Behandlung von rezidivierenden oder refraktären AML, und die laufende entscheidende Phase-3-Studie (die 'MIRACLE'-Studie) stattfinden.
Zu den wichtigsten Teilnehmern gehören das Management-Team von Moleculin und angesehene AML-Experten aus renommierten Institutionen. Die Veranstaltung behandelt Themen wie die Verwendung von Anthrazyklinen, das potenzielle Auswirkungen von Annamycin auf die AML-Behandlung und Details zur globalen Phase-3-Studie. Interessierte können über eine Telefonkonferenz teilnehmen oder das Live-Video-Webcast auf der Website von Moleculin verfolgen.
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Live webcast discussion featuring internationally renowned Acute Myeloid Leukemia (AML) Key Opinion Leaders
Ongoing progress of pivotal, adaptive Phase 3 clinical trial (the "MIRACLE" trial) designed for possible accelerated approval of Annamycin in combination with cytarabine for the treatment of relapsed or refractory AML
For the event, Walter Klemp, Chairman and Chief Executive Officer, and Dr. Paul Waymack, Senior Chief Medical Officer of Moleculin will be joined by key opinion leaders: Michael Andreef, MD, PhD, Professor of Medicine, Department of Stem Cell Transplantation, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center; Dr. Giovanni Martinelli, Associate Professor; Department of Medical and Surgical Sciences, Bologna University; and Mohamad Cherry, MD, Medical Director of Hematology at Atlantic Health System.
As part of the event, the members of the Moleculin Management team and participating KOLs will provide an overview of Annamycin, discuss the use of anthracyclines, how Annamycin could significantly change the AML treatment landscape, and the Company's recently announced global Phase 3 pivotal trial for the treatment of AML patients who are refractory to or relapsed after induction therapy (R/R AML) (the "MIRACLE" trial).
Interested participants and investors may access the conference call by dialing (877) 407-0832 (domestic) or (201) 689-8433 (international) and referencing the Moleculin Biotech Conference Call. A live video webcast of the event will be available on the Events page under the Investors section of the Company's website (moleculin.com). A webcast replay will be available two hours following the live event and will be accessible for 90 days.
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 X, 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. 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.
Investor Contact:
JTC Team, LLC
Jenene Thomas
(908) 824-0775
MBRX@jtcir.com
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SOURCE Moleculin Biotech, Inc.
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