https://www.fiercepharma.com/pharma/lilly-innovent-hit-fda-no-go-discounted-pd-1-immunotherapys-lung-cancer-bid-after-bleak
"In hindsight, Tyvyt’s fate was spelled out for it when director of the FDA’s Oncology Center of Excellence, Richard Pazdur, M.D., penned an article in The New England Journal of Medicine in December questioning the use of clinical data generated solely or predominantly in China to seek U.S. approvals."
Replace 'China' with 'Israel'.
Ann: Positive Pre-IND Guidance from FDA on Zantrene, page-48
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