CONTROLLED SUBSTANCE REGULATION FOR THE COVID-19 MENTAL HEALTH CRISIS

• 成果类型: Article
• 署名作者: Marks, Mason M.
• 署名单位: Gonzaga University; Harvard University
• 刊物名称: ADMINISTRATIVE LAW REVIEW
• ISSN/ISSBN: 0001-8368
• 发表日期: 2020
• 页码: 649-718
• 关键词: PERSISTING PERCEPTION DISORDER; LIFE-THREATENING CANCER; STRESS-DISORDER; PSILOCYBIN TREATMENT; DOUBLE-BLIND; RISK; DEPRESSION; RESISTANT; ANXIETY; APPROVAL

摘要

The COVID-19 pandemic is producing widespread loss of life, unemployment, and social isolation that is triggering a mental health crisis. Experts warn there could be record levels of depression, suicide, and substance use disorders. The US. healthcare system is not prepared. It lacks the resources to provide prolonged psychotherapy at scale, and existing drug treatments are ineffective in about half the people who try them. Amid worsening mental health-related morbidity and mortality, the experimental drugs psilocybin and 3,4-Methylene diagmethamphetamine (MDMA) are an untapped resource. These drugs belong to a class of compounds called the psychedelics, which has been criminalized and stigmatized by the US. war on drugs for over fifty years. The U.S. Drug Enforcement Administration (DEA) classifies them as Schedule I controlled substances with a high potential for abuse and no currently accepted medical uses. However, recent clinical trials conducted in the United States and abroad undermine the DEA's position and suggest that psilocybin and MDMA can safely treat a variety of mental health conditions. Moreover, unlike existing therapies, thy act quickly, and their benefits are often sustained. This Article explores the legal obstacles to administering psilocybin and MDMA to mitigate the COVID-19 mental health crisis. It surveys the scientific evidence for their use and outlines a path toward rapid deployment. Due to the urgent need for effective mental health treatments, the DEA should deschedule psilogbin, reschedule MDMA, and lift annual aggregate production quotas on these drugs. The Food and Drug Administration (FDA) should issue emergency use authorizations (EUAs) for their therapeutic use. To enhance safety, the FDA Commissioner can attach conditions of use to the EUAs, comparable to Risk Evaluation and Mitigation Strategies (REMS), such as requiring psilocybin and MDMA to be administered in controlled settings under professional supervision. Prior to the onset of COVID-19, several cities decriminalized psychedelics while acknowledging their therapeutic benefits. The U.S. Department of justice (DOJ), which enforces violations of the federal Controlled Substances Act (CSA), should pledge not to prosecute individuals who use psychedelics in accordance with state and local laws. Meanwhile, amid growing national scrutiny of law enforcement policies and procedures following high profile police killings, Congress should reevaluate the DOD's prominent role in US. drug policy. It has come to light that the war on drugs rests on a foundation of misinformation and racial animus, which has devasted communities of color. Moreover, due to restrictions on research and development, the drug war adversely impacts people with mental health conditions by depriving them of effective drug therapies. Accordingly, Congress should amend the CSA to shift drug control from law enforcement agencies to science and public-health oriented agencies, such as the FDA and the National Institutes of Health. This restructuring of responsibilities would align federal controlled substance regulation with state drug control, which is overseen by public health agencies instead of law enforcement.