Rajen Mody, MBBS
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About
Dr. Rajen Mody joined the Division of Pediatric Hematology/Oncology following completion of his fellowship training in pediatric hematology/oncology at the University of Michigan. He subsequently completed his Masters in Science (MS) in clinical trials design and biostatistics at the school of public health at the university of Michigan. Before coming to Michigan, Dr. Mody completed a pediatric residency and chief residency at the State University of New York, in New York City. His research interests include new drug development against childhood cancers and role of precision medicine in pediatric oncology.
Additional information:
Rajen Mody, MD, MS, Ruth Heyn Professor of Pediatrics Clinical and MPLAN Medical Director, Pediatric Hematology/Oncology Director, Pediatric Phase-I and Experimental Therapeutics Program Principal Investigator, COG Phase I-III Studies @ UM University of Michigan
Expertise
Locations
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Pediatric Oncology | C. S. Mott Children's Hospital 1540 E Hospital Dr
Floor 7 Reception C
Ann Arbor, MI 48109-4257Get Directions -
Solid Tumor Oncology Program | C. S. Mott Children's Hospital 1540 E Hospital Dr
Floor 4 Reception B
Ann Arbor, MI 48109-4217Get Directions
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University of Michigan Health participates with most health insurance plans.
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Medical School or Training
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Research Overview
Dr. Mody’s primary research interest includes use of precision oncology approach for designing innovative clinical trials for refractory childhood cancers. Dr. Mody is leading a clinical trial investigating the role of next generation sequencing (NGS) in precision oncology for developing novel biomarkers and therapeutic targets against refractory childhood cancers. This effort is being carried out in collaboration with the laboratory of Dr. Arul Chinnaiyan in the Michigan Center of Translational Pathology (MCTP).
Dr. Mody’s other research interest includes development of early phase clinical trials against refractory childhood cancers. He is the Principal Investigator of international Phase-II, randomized trial of Chimeric 14.18 or Temsirolimus in combination with Irinotecan/ Temozolomide through Children’s Oncology Group (COG). He is a member of the High Risk Neurobalstoma Committee of COG, institutional performance review committee for COG Phase-I consortium and is the Principle Investigator of the Children's Oncology Group, Phase-I, Phase II-III Consortium studies at C.S. Mott Children's Hospital.
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