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Nat. Rev. Clin. Oncol. doi:10.1038/nrclinonc.2016.79
Figure 3 Regulatory considerations in trial development of drugs combined with radiotherapy Figure 3 | Regulatory considerations in trial development of drugs combined with radiotherapy. Early interactions with regulatory agencies are recommended because of the limited published regulatory guidance. CHMP, Committee for Medicinal Products for Human Use; EMA, European Medicines Agency; IND, investigational new drug; MOA, mechanism of action; MTD, maximum tolerated dose; NDA, new drug application; PI/PII/PIII, phase of development of clinical trial; RT, radiotherapy. Sharma, R. A. et. al. (2016) Clinical development of new drug–radiotherapy combinations Nat. Rev. Clin. Oncol. doi: /nrclinonc
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