CAMBRIDGE, Mass., Sept. 28, 2016 /PRNewswire/ -- Merrimack Pharmaceuticals, Inc. (Nasdaq: MACK) today announced it will
Merrimack will present the final results of the Phase 3 NAPOLI-1 study in a poster discussion session and a NAPOLI-1 safety-over-time subset analysis in a separate poster session. The primary Phase 3 NAPOLI-1 data were the basis of the US Food and Drug Administration (FDA) and Taiwan FDA approvals of the ONIVYDE® (irinotecan liposome injection) combination regimen in October 2015. It is also the basis of the European Union's Committee for Medicinal Products for Human Use (CHMP) positive opinion issued in July 2016.
Additional ESMO 2016 poster presentations include an evaluation of MM-302's potential for treating HER2-intermediate tumors as well as two trials-in-progress posters, both potentially registrational, for MM-302 and seribantumab, also known as MM-121. MM-302 is an investigational HER2-targeted liposomal encapsulation of doxorubicin from Merrimack's antibody-directed nanotherapeutic platform, while seribantumab is Merrimack's investigational anti-ErbB3 monoclonal antibody that targets heregulin-positive cancer cells within solid tumors.
Poster Discussion Session:
Merrimack is a fully integrated biopharmaceutical company that views cancer as a complex engineering challenge. Through systems biology, which brings together the fields of biology, computing and engineering, Merrimack aims to decrease uncertainty in drug development and clinical validation, and move discovery efforts beyond trial and error. Such an approach has the potential to make individualized treatment of patients a reality. Merrimack's first commercial product, ONIVYDE® (irinotecan liposome injection), was approved by the U.S. FDA in October 2015. With four additional candidates in clinical studies, several in preclinical development and multiple biomarkers designed to support patient selection, Merrimack is building one of the most robust oncology pipelines in the industry. For more information, please visit Merrimack's website at www.merrimack.com or connect on Twitter at @MerrimackPharma.
Any statements in this press release about future expectations, plans and prospects for Merrimack constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995, as amended. Actual results may differ materially from those indicated by such forward-looking statements. Merrimack anticipates that subsequent events and developments will cause its views to change. However, while Merrimack may elect to update these forward-looking statements at some point in the future, Merrimack specifically disclaims any obligation to do so.
Media ContactMarianne McMorrow774firstname.lastname@example.org
Investor ContactGeoffrey Grande, CFA617email@example.com
To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/merrimack-to-present-final-results-of-phase-3-napoli-1-study-at-the-european-society-for-medical-oncology-2016-congress-300335962.html
SOURCE Merrimack Pharmaceuticals, Inc.
Subscribe to our Free Newsletters!