Multivariate Profiling of Complex Biological Regulatory Pathways
Filed on 2003-04-10
Drs. Alan Alfano, Laura Prestia, and Robert Sons, technology transfer rookies at the National Cancer Institute’s (NCI) Technology Transfer Center (TTC), established the first federal Technology Transfer Ambassadors Program (TTAP). The TTAP is a year-long, hybrid training/mentoring program for NCI post-doctoral scientists seeking professional and career development about invention development, commercialization, and entrepreneurship.
NCI TTC:
• Alan Alfano, Ph.D., TTM
• Laura Prestia, Ph.D., TTM
• Robert Sons, Ph.D., TTM
HIV microbicides are not currently sold commercially, and many other HIV prevention techniques remain unavailable or unfeasible in developing countries where the disease is most prevalent. The technology transfer effort of developing large scale production methods of CV-N in soy beans helps to address this issue. The ability to produce CV-N in large quantities at low cost affords researchers the potential to develop effective HIV prevention methods worldwide.
HIV microbicides are not currently sold commercially, and many other HIV prevention techniques remain unavailable or unfeasible in developing countries where the disease is most prevalent. The technology transfer effort of developing large scale production methods of CV-N in soy beans helps to address this issue. The ability to produce CV-N in large quantities at low cost affords researchers the potential to develop effective HIV prevention methods worldwide.
Through a CRADA with EMD Serono, NCI played an instrumental role in developing and
expediting regulatory approval of EMD Serono’s checkpoint inhibitor, avelumab. Avelumab
received FDA approval in 2017, only four years after EMD Serono and NCI added the study of
avelumab to their CRADA. This was a remarkably fast developmental and regulatory approval
timeline.
Through a CRADA with EMD Serono, NCI played an instrumental role in developing and
expediting regulatory approval of EMD Serono’s checkpoint inhibitor, avelumab. Avelumab
received FDA approval in 2017, only four years after EMD Serono and NCI added the study of
avelumab to their CRADA. This was a remarkably fast developmental and regulatory approval
timeline.
Sidra Ahsan, Ph.D., a fellow at the NCI TTC, received the “Rookie
NCI received the “Educational Institution and Federal Laboratory Partnership Award” at the Federal Laboratory Consortium 2018 Mid-Atlantic meeting for the establishment of the “NCI Immunotherapy Fellowship Co-sponsored by Society for Immunotherapy of Cancer.” “The award exemplifies what is possible through engaged partnerships, in this case, TTC, investigators from NCI’s Center for Cancer Research, a CRADA partner and a non-profit,” commented Dr.
The Foundation for the National Institutes of Health (FNIH) besto
In 2011, NCI and Iovance Biotherapeutics entered into a CRADA for the development of Adoptive Cell Therapy (ACT) using Tumor Infiltrating Lymphocytes (TIL). Technology licenses between NCI and Iovance were established to grant Iovance rights to the NIH’s TIL patent estate. By 2019, Iovance began conducting two pivotal multi-center trials of TIL technology in advanced cervical cancer and metastatic melanoma and has achieved Breakthrough Therapy and Fast Track designations from the FDA in these indications, respectively.