However, Gelsinger died from organ failure only a few days after receiving the therapy (Kolehmainen, 2000). Following Gelsinger’s death, the FDA and the NIH conducted an interrogation into the experiment, and found the informed consent document Gelsinger had signed differed from the one the agency approved, as Gelsinger’s document failed to mention that several monkeys had died in previous experiments with the gene therapy (Kolehmainen, 2000). The result of Gelsinger’s death led the NIH to receive “691 reports of ‘serious adverse events’ in gene therapy experiments (Kolehmainen, 2000, para. 10). After receiving the report of Gelsinger’s death, the U.S. Senate Subcommittee on Public Health held a hearing for the gene therapy experiments to learn how to better protect human participants (Rowe,
However, Gelsinger died from organ failure only a few days after receiving the therapy (Kolehmainen, 2000). Following Gelsinger’s death, the FDA and the NIH conducted an interrogation into the experiment, and found the informed consent document Gelsinger had signed differed from the one the agency approved, as Gelsinger’s document failed to mention that several monkeys had died in previous experiments with the gene therapy (Kolehmainen, 2000). The result of Gelsinger’s death led the NIH to receive “691 reports of ‘serious adverse events’ in gene therapy experiments (Kolehmainen, 2000, para. 10). After receiving the report of Gelsinger’s death, the U.S. Senate Subcommittee on Public Health held a hearing for the gene therapy experiments to learn how to better protect human participants (Rowe,