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Underestimation of Harms in Phase I Trials
Published online by Cambridge University Press: 01 January 2021
Abstract
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- Type
- Independent Articles: Commentary
- Information
- Journal of Law, Medicine & Ethics , Volume 47 , Issue 2: Human Subject Protection , Summer 2019 , pp. 334 - 335
- Copyright
- Copyright © American Society of Law, Medicine and Ethics 2019
References
Fisher, J.A. et al., “Appraising Harm in Phase I Trials: Healthy Volunteers' Accounts of Adverse Events,” Journal of Law, Medicine & Ethics 47, no. 2 (2019): 323-333.Google Scholar
Chen, S.C., Sinaii, N., Bedarida, G., Gregorio, M.A., Emanuel, E., and Grady, C., “Phase 1 Healthy Volunteer Willingness to Participate and Enrollment Preferences,” Clinical Trials 14, no. 5 (2017): 537-546, doi: 10.1177/1740774517722131.CrossRefGoogle Scholar
Chen, supra note 2.Google Scholar
Fisher, supra note 1.Google Scholar
Fisher, supra note 1.Google Scholar
Różyżska, J. J., “What Makes Clinical Labour Different? The Case of Human Guinea Pigging,” Journal of Medical Ethics 44, no. 9 (2018): 638-642, doi:10.1136/medethics-2017-104267.CrossRefGoogle Scholar
Fisher, supra note 1.Google Scholar
Eaton, A., Iasonos, A., Gounder, M.M., Pamer, E.G., Drilon, A., Vulih, D., Smith, G.L., Ivy, S.P., Spriggs, D.R., and Hyman, D.M., “Toxicity Attribution in Phase I Trials: Evaluating the Effect of Dose on the Frequency of Related and Unrelated Toxici-ties,” Clinical Cancer Research 22, no. 3 (2016): 553-559, doi: 10.1158/1078-0432.CCR-15-0339.CrossRefGoogle Scholar
Waligora, M. et al., “Risk and Surrogate Benefit for Pediatric Phase I Trials in Oncology: A Systematic Review with Meta-Analysis,” PLOS Medicine 15, no. 2 (2018): e1002505, doi:10.1371/journal.pmed.1002505.CrossRefGoogle Scholar