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COVID-19 International Clinical Trial Received Regulatory Approval to Begin Research

Germantown, MD, USA (September 29, 2020) – Amarex Clinical Research, LLC, an NSF International company, is supporting their client RevImmune, Inc. in the conduct of a Phase 2 clinical trial testing a treatment for patients with COVID-19. The ILIAD-7 trial is researching if human recombinant interleukin-7 [IL-7] can boost the immune system’s ability to fight coronavirus infection by increasing the numbers and function of white blood cells known as lymphocytes. Patients have been enrolled in the UK (where it has been designated as an Urgent Public Health priority by the UK Chief Medical Officer), France, and now the U.S. Amarex has worked with RevImmune to setup and conduct this international trial.

Dr. Kazem Kazempour, Amarex President & CEO, stated, “This is a patient population with a high unmet medical need. It is rewarding for Amarex to assist with this international effort by obtaining multiple regulatory approvals to conduct this clinical trial, using a product from a European company.”

This is Amarex’s third clinical trial for therapeutic products treating COVID-19 in the US. The other two COVID-19-related trials are testing a monoclonal antibody drug. Amarex has also submitted multiple other drug and device applications to the U.S. FDA and other health regulatory agencies for either treatment or diagnosis of COVID-19 and expects to begin more trials shortly.

About Amarex Clinical Research, LLC, an NSF International company

Amarex Clinical Research, LLC, an NSF International company, is a global, full service Contract Research Organization (CRO), whose leadership team has significant expertise conducting biomedical research, and whose combined experience includes the design and conduct of several hundred clinical research projects in many therapeutic indications. Amarex provides comprehensive services in Project Management (Phase I-IV, BE/BA, PK/PD), Regulatory Affairs (FDA Applications and meetings, Applications to International Health Authorities, GxP Compliance Audits), Clinical Operations, Adaptive Study Designs, Statistical Analysis, Data Management, Medical Monitoring, Safety and Pharmacovigilance, and General Consulting. Amarex can take your product through the entire approval process, from creating the regulatory approval strategy, to conducting trials, to writing the marketing approval application. Join our growing list of clients with approved products. Amarex provides high quality and cost efficient services. For more information visit www.amarexus.com.

Amarex Contact:
Patrick J. Burke
Business Development
patrickb@amarexcro.com

20201 Century Blvd., Fourth Floor
Germantown, MD 20874 USA
301 528 7000
www.amarexus.com

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