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For its part, FDA proposed a pilot program where qualified external institutions can collaborate with sponsors to develop and review protocols for first-in-human (FIH) clinical trials intended for investigational new drug (IND) submissions, and several associated draft guidances, including one clarifying when developers can rely on one rigorous, adequate, and well-controlled clinical trial, along with confirmatory evidence, to support drug approvals

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The peptide reduces not only tumor growth, but also delivery and spread to distant tissues

doi: 10.1016/j.cell.2017.12.030 97 HardimanO.Al-ChalabiA.ChioA.CorrE