TABLE 1.
Workshop Speakers and Presentationsa
Speakers | Representing/affiliation | Title |
---|---|---|
| ||
C. Norman Coleman, MD | National Cancer Institute | Poly pharmacy: How might this need be considered for a major nuclear or radiological incident that could produce the acute radiation syndrome? |
Steven A. Adams, MPH | ASPR | Strategic National Stockpile, support for the response to a nuclear incident |
Christie M. Orschell, PhD | Indiana University School of Medicine | Defining the hematopoietic acute radiation syndrome and the delayed effects of acute radiation exposure in murine models |
Thomas MacVittie, PhD | University of Maryland School of Medicine | The acute radiation syndrome in the nonhuman primate: Is ARS multi-organ injury (MOI) linked to the MOI characteristic of the delayed effects of acute radiation exposure? |
J. Mark Cline, DVM, PhD, DACVP | Wake Forest School of Medicine | Multisystemic delayed effects of acute radiation exposure in nonhuman primates |
George (Joe) Cox, PhD | Bolder Biotechnology, Inc. | Improving survival in a mouse H-ARS model using combinations of hematopoietic growth factors and an ACE inhibitor |
Meetha Medhora, PhD | Medical College of Wisconsin | Enhanced mitigation of radiation-induced injuries by combining angiotensin-converting enzyme (ACE) inhibitors with other countermeasures |
Juliann Kiang, PhD | AFRRI | Combined drugs with the pegylated-G-CSF therapy to enhance survival and against multi-organ injury after irradiation alone or combined with wound trauma |
Yon Yu, PharmD | CDC | Regulatory considerations for emergency use of stockpiled medical countermeasures |
Mario Sampson, PharmD | CDER, FDA | Clinical pharmacology considerations for products developed for acute radiation syndrome |
Adebayo Laniyonu, PhD | CDER, FDA | Product development for acute radiation syndrome: Nonclinical considerations for animal rule efficacy studies |
Workshop participants had an opportunity to review this meeting report prior to journal submission.