Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06656702 · ClinicalTrials.gov registry record · Early Phase 1

Effects of Psilocybin in Patients With Amyotrophic Lateral Sclerosis

A Early Phase 1 study of Amyotrophic Lateral Sclerosis, sponsored by Johns Hopkins University.

Recruiting
Registry status
Early Phase 1
Development phase
24
Enrollment target
1
Study location

NCT06656702: Recruiting Early Phase 1 study of Amyotrophic Lateral Sclerosis, sponsored by Johns Hopkins University.

NCT06656702 is a Early Phase 1 study of Amyotrophic Lateral Sclerosis that is actively recruiting participants, run by Johns Hopkins University. The registered enrollment target is 24 participants, below the 898-participant average among 102 other Amyotrophic Lateral Sclerosis trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06656702, a Early Phase 1 study of Amyotrophic Lateral Sclerosis, is actively recruiting participants, sponsored by Johns Hopkins University.

RECRUITING
Registry status
Early Phase 1
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

This study aims to study the feasibility of psilocybin therapy for patients with Amyotropic Lateral Sclerosis (ALS) with depressed mood. The secondary objective is to assess its impact on depression, quality of life, hopelessness, and functional status in this patient population.

Primary Outcome

feasibility will be assessed by participant recruitment, retention, and treatment adherence.

Interventions

  • DRUG Psilocybin

Study Locations (1)

Maryland

  • Johns Hopkins Center for Psychedelic and Consciousness Research - Baltimore

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2025-04-09
Est. Completion 2027-07-01
Phase Early Phase 1
Johns Hopkins University

1,448 total trials

What NCT06656702 shows while recruiting

NCT06656702 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 898-participant average among 102 other Amyotrophic Lateral Sclerosis trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Amyotrophic Lateral Sclerosis appearing as the primary indexed condition, and to 1 intervention - of which Psilocybin is the first listed.

NCT06656702 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT06656702 about?

NCT06656702 is a clinical study titled "Effects of Psilocybin in Patients With Amyotrophic Lateral Sclerosis". This study aims to study the feasibility of psilocybin therapy for patients with Amyotropic Lateral Sclerosis (ALS) with depressed mood. The secondary objective is to assess its impact on depression, quality of life, hopelessness, and functional status in this patient population.

What is the current status of trial NCT06656702?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 24 participants. The study started on 2025-04-09. Estimated completion is 2027-07-01.

What conditions does trial NCT06656702 study?

This clinical trial studies the following conditions: Amyotrophic Lateral Sclerosis.

What interventions are being tested in trial NCT06656702?

The interventions under investigation include: Psilocybin (DRUG).

Who is sponsoring clinical trial NCT06656702?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06656702 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Amyotrophic Lateral Sclerosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06656702's enrollment target sits among peer trials

24 73rd of 102 higher than 30 of 102 other Amyotrophic Lateral Sclerosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Amyotrophic Lateral Sclerosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06656702, the US trial registry maintained by the National Library of Medicine. NCT06656702 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.