MDMA-assisted therapy for severe PTSD: a randomized, double-blind, placebo-controlled phase 3 study

被引:433
|
作者
Mitchell, Jennifer M. [1 ,2 ]
Bogenschutz, Michael [3 ]
Lilienstein, Alia [4 ]
Harrison, Charlotte [5 ]
Kleiman, Sarah [6 ]
Parker-Guilbert, Kelly [7 ]
Ot'alora, Marcela G. [8 ,9 ]
Garas, Wael [8 ]
Paleos, Casey [10 ]
Gorman, Ingmar [11 ]
Nicholas, Christopher [12 ]
Mithoefer, Michael [5 ,9 ,13 ]
Carlin, Shannon [5 ,9 ]
Poulter, Bruce [8 ,9 ]
Mithoefer, Ann [9 ]
Quevedo, Sylvestre [2 ,14 ]
Wells, Gregory [14 ]
Klaire, Sukhpreet S. [15 ]
van der Kolk, Bessel [16 ]
Tzarfaty, Keren [9 ]
Amiaz, Revital [17 ]
Worthy, Ray [18 ]
Shannon, Scott [19 ]
Woolley, Joshua D. [2 ]
Marta, Cole [20 ]
Gelfand, Yevgeniy [21 ]
Hapke, Emma [22 ]
Amar, Simon [23 ]
Wallach, Yair [24 ]
Brown, Randall [11 ]
Hamilton, Scott [25 ]
Wang, Julie B. [5 ]
Coker, Allison [1 ,5 ]
Matthews, Rebecca [5 ]
de Boer, Alberdina [5 ]
Yazar-Klosinski, Berra [4 ]
Emerson, Amy [5 ]
Doblin, Rick [4 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Psychiat & Behav Sci, San Francisco, CA 94143 USA
[3] NYU, Dept Psychiat, Grossman Sch Med, 550 1St Ave, New York, NY 10016 USA
[4] Multidisciplinary Assoc Psychedel Studies MAPS, San Jose, CA USA
[5] MAPS Publ Benefit Corp MAPS PBC, San Jose, CA USA
[6] Kleiman Consulting & Psychol Serv, Sayreville, NJ USA
[7] KPG Psychol Serv LLC, Brunswick, ME USA
[8] Aguazul Bluewater Inc, Boulder, CO USA
[9] MAPS Publ Benefit Corp, MDMA Therapy Training Program, San Jose, CA USA
[10] Nautilus Sanctuary, New York, NY USA
[11] Fluence, Woodstock, NY USA
[12] Univ Wisconsin, Sch Med & Publ Hlth, Dept Family Med & Community Hlth, Madison, WI USA
[13] Med Univ South Carolina, Charleston, SC 29425 USA
[14] San Francisco Insight & Integrat Ctr, San Francisco, CA USA
[15] British Columbia Ctr Subst Use, Vancouver, BC, Canada
[16] Boston Univ, Sch Med, Boston, MA 02118 USA
[17] Chaim Sheba Med Ctr, Tel Hashomer, Israel
[18] Ray Worthy Psychiat LLC, New Orleans, LA USA
[19] Wholeness Ctr, Ft Collins, CO USA
[20] New Sch Res LLC, North Hollywood, CA USA
[21] Zen Therapeut Solut, Mt Pleasant, SC USA
[22] Univ Toronto, Toronto, ON, Canada
[23] Dr Simon Amar Inc, Montreal, PQ, Canada
[24] Beer Yaakov Ness Ziona Mental Hlth Ctr, Beer Yaagov, Israel
[25] Stanford Sch Med, Stanford, CA 94305 USA
关键词
POSTTRAUMATIC-STRESS-DISORDER; PSYCHOTHERAPY; POLYMORPHISM; EFFICACY; DROPOUT; ECSTASY; SAFETY;
D O I
10.1038/s41591-021-01336-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Post-traumatic stress disorder (PTSD) presents a major public health problem for which currently available treatments are modestly effective. We report the findings of a randomized, double-blind, placebo-controlled, multi-site phase 3 clinical trial (NCT03537014) to test the efficacy and safety of 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy for the treatment of patients with severe PTSD, including those with common comorbidities such as dissociation, depression, a history of alcohol and substance use disorders, and childhood trauma. After psychiatric medication washout, participants (n = 90) were randomized 1:1 to receive manualized therapy with MDMA or with placebo, combined with three preparatory and nine integrative therapy sessions. PTSD symptoms, measured with the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5, the primary endpoint), and functional impairment, measured with the Sheehan Disability Scale (SDS, the secondary endpoint) were assessed at baseline and at 2 months after the last experimental session. Adverse events and suicidality were tracked throughout the study. MDMA was found to induce significant and robust attenuation in CAPS-5 score compared with placebo (P < 0.0001, d = 0.91) and to significantly decrease the SDS total score (P = 0.0116, d = 0.43). The mean change in CAPS-5 scores in participants completing treatment was -24.4 (s.d. 11.6) in the MDMA group and -13.9 (s.d. 11.5) in the placebo group. MDMA did not induce adverse events of abuse potential, suicidality or QT prolongation. These data indicate that, compared with manualized therapy with inactive placebo, MDMA-assisted therapy is highly efficacious in individuals with severe PTSD, and treatment is safe and well-tolerated, even in those with comorbidities. We conclude that MDMA-assisted therapy represents a potential breakthrough treatment that merits expedited clinical evaluation. Results from a phase 3, double-blind, randomized, placebo-controlled trial demonstrate that MDMA-assisted therapy is safe and effective in treating severe post-traumatic stress disorder.
引用
收藏
页码:1025 / +
页数:15
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