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ClinicalRM will again deploy its boots-on-the-ground approach to fighting Ebola Virus Disease (EVD) with an expanded access protocol for ZMappTM, an investigational treatment for EVD, in Africa and the U.S.
ClinicalRM will perform as subcontractor under federally funded Contract No. HHSO100201600021C, awarded to Mapp Biopharmaceutical Inc. (Mapp) by the Biomedical Advanced Research and Development Authority (BARDA), Office of the Assistant Secretary for Preparedness and Response, Office of the Secretary, Department of Health and Human Services, to assist in carrying out an expanded access protocol for ZMappTM, a cocktail of three monoclonal antibodies being developed by Mapp/LeafBio to treat EVD.
This award is the latest instance of government and industry calling for ClinicalRM’s expertise in combating global health crises. The ZMappTM protocol will take place in some of the historically hardest-hit areas for EVD – Sierra Leone, Liberia and Guinea – as well as at least three sites in the U.S. ClinicalRM’s tasks include training staff at study sites, monitoring the safety of study participants and managing the safe storage and shipping of the experimental product, particularly during periods when there are no EVD-positive patients. ClinicalRM’s Global Infrastructure Development (GID) group will ensure the capabilities of the African sites to perform the work and may make necessary infrastructure, laboratory, technology and operational improvements. The study may require ClinicalRM to mobilize rapid-response treatment units, working in the field to administer ZMappTM to patients in situations where EVD cases occur in remote areas.
“Our involvement in this study is an acknowledgement of the expertise we gained during the 2014 outbreak working with EVD and the research environment in West Africa,” ClinicalRM President Joseph Sgherza said. “Our GID group’s motto – and goal – is ‘Leave Something Behind.’ We didn’t simply bring in bloodmobiles and staff as a temporary fix until the crisis was over – we stayed to build a sustainable structure of labs, supply chains, communications systems and highly trained clinicians that can now support research projects from sponsors around the world.”
As therapeutic options for EVD are extremely limited, potent agents to treat patients with EVD are needed. Of the experimental agents that have demonstrated survival benefit in non-human primate models, ZMappTM is one of the most promising therapeutic interventions developed to date.
About ClinicalRM
ClinicalRM is a full-service Contract Research Organization specializing in preclinical-through-Phase-IV support of clinical research and clinical trial services for biologics, drugs and devices. The organization helps customers get their products to market faster with a wide array of global research, regulatory and sponsor services. From international partnerships and affiliates to government relations and local alliances, ClinicalRM delivers specialized collaborations and a distinct ability to provide rapid-response efforts to global health crises. With registered branch offices in Sierra Leone and Liberia, ClinicalRM is known internationally for its efforts during the 2014 West Africa EVD outbreak, coupled with its ongoing EVD projects in the region funded by the Bill and Melinda Gates Foundation. To learn more, visit www.clinicalrm.com.
Contacts
ClinicalRM
Amy Trotch
Marketing & Business Development Manager
800-431-9640, x229
