Abstract
The outbreak of the Coronavirus disease (COVID-19) pandemic has deeply challenged healthcare systems and care of patients with cancer. Phase 1 studies are among the most complicated clinical trials and require thorough patient selection, as well as intensive patient monitoring. In this perspective, we discuss the key factors that should be considered for the conduct of phase 1 trials and management of COVID-19–positive patients with cancer enrolled in such trials. We notably present the risks and challenges raised by COVID-19–infected phase 1 patients, in terms of safety, toxicity causality assessment, drug efficacy evaluation and clinical research priorities. We finally propose some guidelines for the conduct of phase 1 trials and management of COVID-19–infected patients in a pandemic time.
【저자키워드】 COVID-19, SARS-CoV-2, Drug development, Phase 1, 【초록키워드】 clinical trial, pandemic, risk, Toxicity, outbreak, management, Research, Patient, disease, Intensive, Care, patients, trials, Healthcare system, Patients with cancer, Drug efficacy, Perspective, phase 1 trial, key factor, patient selection, enrolled, raised, 【제목키워드】 outbreak, Patient, disease,