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Christopher R. Nicholas

16 papers in the library · 1,136 citations · publishing 2017-2026

Papers

MDMA-assisted therapy for moderate to severe PTSD: a randomized, placebo-controlled phase 3 trial.

Nature medicine October 1, 2023 Jennifer M. Mitchell, Marcela Ot’alora G., Bessel Van der Kolk et al. 400 citations

In a phase 3 trial, MDMA-assisted therapy reduced PTSD symptoms and functional impairment more than placebo with therapy in 104 participants with moderate to severe PTSD. The average decrease in PTSD symptom severity was 23.7 points with MDMA-assisted therapy versus 14.8 points with placebo, and functional disability improved by 3.3 versus 2.1 points. Participants were ethnoracially diverse, with 27% identifying as Hispanic/Latino and 34% as other than White. Severe side effects occurred in 9.4% of the MDMA group and 3.9% of the placebo group; no deaths or serious adverse events were reported. The treatment was generally well tolerated.

The experimental effects of psilocybin on symptoms of anxiety and depression: A meta-analysis

Psychiatry Research January 2, 2020 Simon B. Goldberg, Brian T. Pace, Christopher R. Nicholas et al. 234 citations

A meta-analysis of four studies (three randomized, placebo-controlled; one uncontrolled) with 117 participants found that psilocybin combined with behavioral interventions produced large reductions in anxiety and depression among people with elevated symptoms. Within-group effects from before treatment to after treatment and at follow-up were large (Hedges' g = 1.16 to 1.47) and statistically significant. Across the placebo-controlled studies, the pre-post effects compared to placebo were also large (g = 0.82 to 0.83) and statistically significant. No serious adverse events were reported. The results tentatively support further research on psilocybin for anxiety and depression, though the small number of studies and potential bias limit confidence.

Pharmacokinetics of Escalating Doses of Oral Psilocybin in Healthy Adults

Clinical Pharmacokinetics March 28, 2017 Randall Brown, Christopher R. Nicholas, Nicholas V. Cozzi et al. 189 citations

Psilocybin is a psychedelic tryptamine being studied for depression and substance use disorders. In an open-label study of 12 healthy adults, escalating oral doses of 0.3, 0.45, and 0.6 mg/kg were given at monthly intervals. No psilocybin was found in plasma or urine; its active metabolite psilocin had an elimination half-life of 3 hours (standard deviation 1.1). Renal clearance of intact psilocin accounted for less than 2% of total clearance, indicating no dose reduction is needed for mild-moderate renal impairment. Body weight did not predict variation in psilocin clearance. No serious adverse events occurred. A fixed 25 mg dose approximates the exposure of a 0.3 mg/kg dose.

High dose psilocybin is associated with positive subjective effects in healthy volunteers

Journal of Psychopharmacology June 27, 2018 Christopher R. Nicholas, Kelsey M. Henriquez, Michele Gassman et al. 85 citations

Healthy participants given escalating doses of psilocybin (0.3, 0.45, and 0.6 mg/kg) showed a significant linear dose-related increase in Mystical Experience Questionnaire total score and the transcendence of time and space subscale, but not in the rate of complete mystical experiences. Dose 3 produced significantly higher transcendence of time and space scores than dose 1, while no dose-related differences emerged for total scores or mystical experience rate. Positive persisting effects 30 days after the last dose were significantly higher than negative ones, and a moderate increase in well-being or life satisfaction was associated with the maximum mystical experience score. Pharmacokinetic measures correlated with dose but not with mystical experience scores or rate, indicating that a complete mystical experience was not necessary for positive outcomes.

THE EFFECTS OF MDMA-ASSISTED THERAPY ON ALCOHOL AND SUBSTANCE USE IN A PHASE 3 TRIAL FOR TREATMENT OF SEVERE PTSD

Drug and Alcohol Dependence February 1, 2022 Christopher R. Nicholas, Julie B. Wang, A. Coker et al. 67 citations

MDMA-assisted therapy for severe PTSD may also reduce hazardous alcohol use without increasing illicit drug use. In a randomized trial, 90 adults with severe PTSD received either MDMA-assisted therapy or placebo plus therapy. Those in the MDMA group showed a greater reduction in alcohol use scores (average decrease of 1.02 points) compared to a slight increase in the placebo group (average increase of 0.40 points). Changes in drug use scores did not differ between groups. The findings suggest MDMA-assisted therapy could serve as an integrated treatment for co-occurring PTSD and alcohol or substance use disorders.

Post-acute psychological effects of classical serotonergic psychedelics: a systematic review and meta-analysis

Psychological Medicine November 4, 2020 Simon B. Goldberg, Benjamin Shechet, Christopher R. Nicholas et al. 66 citations

Classical psychedelics such as psilocybin, ayahuasca, and LSD produce significant psychological effects lasting at least 24 hours after administration, according to a systematic review and meta-analysis of 34 experimental studies involving 549 participants. Large effects were observed for reducing targeted symptoms in psychiatric samples, improving negative and positive affect, social outcomes, and existential or spiritual well-being, with between-group effect sizes ranging from Hedges' g = 0.84 to 1.08. Effects may be larger in clinical samples. Evidence for changes in personality traits or mindfulness was weak. No post-acute adverse effects were found, but high risk of bias, heterogeneity, and possible publication bias underscore the need for larger, placebo-controlled trials.

Misinterpretations and Omissions: A Critical Response to Goodwin and Colleagues' Commentary on Psilocybin-Assisted Therapy.

Am J Psychiatry January 1, 2024 Kelley C. O’donnell, Brian T. Anderson, Frederick S. Barrett et al. 31 citations

This critical response addresses misinterpretations and omissions in a commentary by Goodwin and colleagues on psilocybin-assisted therapy, arguing that the commentary misrepresents existing evidence and overlooks key methodological issues. The authors contend that the commentary fails to adequately discuss safety concerns, including adverse events and the potential for psychological distress, and omits important data on long-term outcomes. They emphasize the need for rigorous, balanced evaluation of psilocybin-assisted therapy's risks and benefits, cautioning against overstating positive outcomes while underreporting negative findings. The response calls for more transparent reporting and careful interpretation of clinical trial results.

Psychotherapy in Psychedelic Treatment: Safe, Evidence-Based, and Necessary.

Am J Psychiatry January 1, 2024 Michael D. Alpert, Kelley C. O’donnell, Casey A. Paleos et al. 22 citations

Psychotherapy is a necessary component of psychedelic treatment, providing safety and evidence-based support. The text argues that integrating structured psychological guidance with psychedelic sessions enhances therapeutic benefits and improves mental health outcomes. This combined approach fosters a supportive journey, leading to transformative mental health care and healing potential.

Exploring psilocybin-assisted psychotherapy in the treatment of methamphetamine use disorder

Frontiers in Psychiatry March 14, 2023 Jonathan Brett, Elizabeth Knock, Paul Liknaitzky et al. 16 citations

Methamphetamine use disorder is a chronic condition with high relapse rates and limited effective treatments. Contingency management and psychotherapy show modest efficacy, while pharmacological options have little to no benefit. Psilocybin-assisted psychotherapy is emerging as a promising approach for substance use disorders, though no studies have yet examined it for methamphetamine use disorder. This review presents the rationale for using psilocybin-assisted psychotherapy to treat methamphetamine use disorder and describes practical considerations from early experience designing and implementing four clinical trials on this approach.

A Field-Wide Review and Analysis of Study Materials Used in Psilocybin Trials: Assessment of Two Decades of Research

Psychedelic Medicine January 20, 2025 Marianna Graziosi, Gabrielle Agin-Liebes, Mary P Cosimano et al. 9 citations

Psilocybin and other serotonergic psychedelics are used in research settings with safety measures including controlled environments, staff presence, screening, and psychoeducation. An analysis of study materials from psilocybin trials over the past two decades found that psychoeducation documents varied but commonly emphasized biological and physical safety, psychological safety and well-being, aspects of setting, and the potential for expectancies. The materials prioritized biological and psychological safety across all sites. The authors also identified elements unrelated to safety that may contribute to participant expectancies and suggest these extrapharmacological factors be studied systematically to maximize safety while minimizing extraneous expectancies.

Psilocybin for Opioid Use Disorder in Two Adults Stabilized on Buprenorphine: A Technical Report on Study Modifications and Preliminary Findings

Psychedelic Medicine December 1, 2023 Julia Malicki, Amelia Baltes, Christopher R. Nicholas et al. 7 citations

A clinical trial found that giving psilocybin together with buprenorphine to people with opioid use disorder was safely tolerated and did not interfere with buprenorphine's effectiveness or psilocybin's subjective effects. The study faced feasibility challenges that required changes to the participant pool and eligibility rules, along with strategies to improve accessibility, reduce burden, and increase generalizability.

How do psychedelics impact people with a history of non-affective psychosis? A qualitative study.

Front Psychiatry December 9, 2025 Haley Maria Dourron, Heith Copes, Daniel H. Grossman et al. 3 citations

People diagnosed with non-affective psychotic disorders who used psychedelics reported a mix of positive and negative effects. Common challenges during the acute experience included transient anxiety, sometimes leading to brief hospitalizations. Some participants described psychosis-specific experiences such as reduced self-stigma and insight into their hallucinations and delusions. Perceived long-term benefits varied widely, with some reporting lasting positive changes and others noting negative effects or no lasting impact. The findings suggest psychedelics may pose both risks and potential benefits for this population, highlighting the need for careful safety trials.

Co-administration of midazolam and psilocybin: Differential effects on subjective quality versus memory of the psychedelic experience

bioRxiv (Cold Spring Harbor Laboratory) June 13, 2024 Christopher R. Nicholas, Matthew I. Banks, Richard Lennertz et al. 3 citations preprint

Co-administering the amnestic benzodiazepine midazolam with psilocybin in 8 healthy participants partially impaired memory for the psychedelic experience while still allowing a conscious experience to occur. The degree of memory impairment was inversely associated with salience, insight, and well-being induced by psilocybin. These results suggest that memory of the acute psychedelic experience contributes to therapeutically relevant behavioral effects. Because midazolam blocks memory by blocking cortical neural plasticity, it may also help evaluate how the pro-neuroplastic properties of psychedelics contribute to their therapeutic activity.

Do Psychedelics Mimic Psychosis? Perspectives on Similarities and Differences from Individuals with Lived Experience of Psychosis and Psychedelics

International Journal of Mental Health and Addiction March 17, 2026 Haley Maria Dourron, Melissa K. Bradley, Heith Copes et al.

Interviews with 19 people diagnosed with non-affective psychotic disorders who had used psychedelics revealed that, while some similarities exist in altered thinking and meaning attribution, most participants reported that psychedelic experiences did not closely resemble their psychosis. Sensory alterations, emotional experience, sense of control, and self-experience were points of contrast. When asked which drug most resembled their psychotic symptoms, the majority endorsed cannabis, followed by dissociative anesthetics and stimulants. The findings suggest that psychedelics may not accurately model many symptoms of psychosis and that interpreting psychedelic experiences as broadly psychosis-like may be misleading.

Electrophysiological effects of psilocybin co-administered with midazolam

bioRxiv (Cold Spring Harbor Laboratory) July 29, 2025 May Kung Sutherland, Christopher R. Nicholas, Richard Lennertz et al. preprint

Psilocybin, a serotonergic psychedelic, induces neural plasticity and alters consciousness, while midazolam, a benzodiazepine, blunts plasticity and causes sedation and amnesia. In an open-label pilot study, 25 mg of oral psilocybin was given alongside intravenous midazolam at doses that allowed a full psychedelic experience but reduced memory of it. EEG recordings showed that 15-30 minutes after dosing, when midazolam was at its target concentration, beta power increased and the spectral exponent decreased. As psilocybin's effects emerged over the next six hours, Lempel-Ziv complexity and spectral exponent increased while broadband power decreased. These findings suggest psilocybin's effects persist even with midazolam, supporting its use in mechanistic studies.