Dr. John Powderly II, Medical Oncologist, Certified Physician Investigator, and Founder and President of Carolina BioOncology Institute and BioCytics, realized early on in his medical career that he felt a strong passion for cellular therapies. As a 4th year medical student interning under the mentorship of immunotherapy pioneer Dr. Steven Rosenberg at the National Cancer Institute, Dr. Powderly first started working with cellular therapies in the mid-1990s and has since dedicated his career to this therapeutic area. Shortly after completing his oncology fellowship at University of North Carolina, Chapel Hill, Dr. Powderly founded the Carolina BioOncology Institute (CBOI) in 2005 as a community-based clinic specializing in early phase immunotherapy and cellular therapy trials. Located in Charlotte, North Carolina, CBOI is the only independent phase I cancer center with cellular manufacturing capabilities on the east coast and serves as a regional hub for access to phase I trials in the community setting.
Providing comprehensive and quality patient care while developing cellular therapies to treat solid tumors.
© 2025 | Carolina BioOncology Institute | A BioCytics Parent Company | All Rights Reserved
Huntersville, NC, November 18, 2025—BioCytics is pleased to announce they successfully reached a regulatory milestone for de-risking clinical development plans with a productive FDA INTERACT meeting during which they discussed manufacturing immune cell therapies at the point of care.
This INTERACT (INitial Targeted Engagement for Regulatory Advice on CBER/CDER ProducTs) meeting is a first step in getting feedback from the FDA regarding the feasibility of BioCytics’ cell therapy platform development plans. By accepting this meeting and reviewing the plans, the FDA is indicating that BioCytics’ immuno-oncology tumor treatment protocol efforts, the first of which is called BioCytics Immune Fraction #1 (BCyIF-1), show enough pre-clinical scientific potential to warrant continued research development and upscaling manufacturing efforts. This milestone feedback from the FDA speaks volumes for BioCytics’ work towards a future Investigational New Drug (IND) submission. It solidifies plans of getting to first-in-human clinical trials in 2027, with the ultimate goal of treating solid tumors.
Dr. John Powderly, Oncologist and President of BioCytics said “We are delighted to have received insightful feedback from the FDA regarding development of BioCytics BCyIF-1, a cellular therapy to be manufactured at the point of care. The FDA’s willingness to review our pre-clinical research data and hold the INTERACT meeting with us results in substantially reduced regulatory risk as we move towards a future IND. It is fantastic to have our early research validated and to be able to enter confidently into our IND-enabling and manufacturing efforts.”
About BioCytics, Inc.
BioCytics, founded in 2005, is a privately held health technology company located in Huntersville, North Carolina. BioCytics is researching autologous Adaptive Cell Therapy (AACT) to develop an immuno-oncology platform for treating solid tumors with the patient’s own immune cells. AACT is a revolutionary point-of-care cell manufacturing process designed to generate nongenetically modified effector cell fractions for all stages of all solid tumors. For more information, please visit Biocytics.com or find us on LinkedIn.
About Carolina BioOncology Institute, PLLS
Carolina BioOncology Institute (CBOI), a cancer treatment and clinical trial facility, is co-located with BioCytics, in Huntersville, NC. CBOI is an independent community-based cancer research clinic that serves the Southeast region as a referral hub for metastatic cancer patients’ access to Phase I clinical research trials. For more information, please visit Carolinabiooncology.org or LinkedIn.
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Jennifer Montague
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