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Kanneboyina Nagaraju, DVM, PhD

Co-founder and Board Member

Dr. Nagaraju is a veterinarian and immunologist with expertise in the molecular pathogenesis of autoimmune and genetic muscle diseases. He is the Founding Chair and Professor of Pharmaceutical Sciences at Binghamton University, NY. He was recently a tenured Professor of Integrative Systems Biology and Pediatrics at George Washington University School of Medicine and Health Sciences, and Associate Director of the Center for Genetic Medicine Research. There he established and directed the preclinical drug testing facility at the Children’s National Medical Center, which has now been transferred to AGADA Biosciences.

Before joining CNMC in 2005, he was an Assistant Professor of Medicine at the Division of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine. Dr. Nagaraju’s research led to the identification of novel anti-inflammatory and membrane-stabilizing compounds that show efficacy in muscular dystrophy as well as inflammatory disease models.

He has led international efforts on the development of standard operating procedures for preclinical efficacy studies. He currently serves as a preclinical expert on the TREAT-NMD Advisory Committee for Therapeutics (TACT) and as a member of the Medical Advisory Committee of Muscular Dystrophy Association and the Scientific Advisory Committee of Cure Duchenne. He also co-founded ReveraGen Biopharma, a biotech company engaged in developing therapeutics for neuromuscular and inflammatory diseases. He currently serves as a consultant for several biotech companies. A list of publications by Dr. Nagaraju is viewable here, and he holds several federal and non-federal grants for translational research on neuromuscular diseases.

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To learn how AGADA Biosciences could support your program, get in touch with our team and start the conversation.

Why AGADA?

We bring dedicated expertise to programs where there is little room for error, providing the scientific support, responsiveness and program fit that help rare disease teams move forward with clarity.

Decade of specialization:

Founded in 2013 as a spinout from Children’s National Medical Center to provide specialist scientific support for rare disease drug development.

Consistent audit success:

We successfully pass an average of five sponsor audits annually to support clinical trials across multiple phases.

Historical benchmarking:

We leverage archival data from over 100 trials in mouse models of muscular dystrophy to accurately power your efficacy studies.

Dedicated scale:

We operate with a team of approximately 50 employees, entirely focused on executing complex rare disease programs.

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Sadish Srinivassane, MSc, MVPH, DVM

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Chris Rice, BSc

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