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FDA approval phases 1, 2, and 3 clinical trials requires companies to conduct large-scale studies to determine safety and efficacy

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Labeled HT-29 cells were pretreated with PBS, PV2, ncAA-nanobody, PV2-PV3 fusion nanobodies and Durvalumab served as positive controls and seeded onto 12-well culture plate at 2 10 5 cells per well (macrophage tumor cell ratio: 1:4)

10.1186/s12891-017-1477-5 16 BloomerR

Meng, H

The method of embodiment9, wherein the macrolide antibiotic is erythromycin