AzTrials
AzTrials

HealthyPhase 12C-BNCT05523401

Acute Effects of 2C-B Compared With MDMA and Psilocybin in Healthy Subjects

A Phase 1 study testing 4-bromo-2,5-dimethoxyphenethylamine (10 mg), 4-bromo-2,5-dimethoxyphenethylamine (20 mg) and 4-bromo-2,5-dimethoxyphenethylamine (30 mg) in people with Healthy, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

4-bromo-2,5-dimethoxyphenethylamine (2C-B) is a psychoactive substance with reportedly similar acute effects to both the prototypical empathogen 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy) and the classic psychedelic substance psilocybin (contained in "magic, hallucinogenic mushrooms"). Read more about this study

Who is it for?
Ages 25 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
4-bromo-2,5-dimethoxyphenethylamine (10 mg), 4-bromo-2,5-dimethoxyphenethylamine (20 mg) and 4-bromo-2,5-dimethoxyphenethylamine (30 mg)
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
24 participants
Where
1 siteSwitzerland
Study dates
16 Aug 2023to 5 Nov 2024
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age between 25 and 65 years.
  • Sufficient understanding of the German language.
  • Understanding the procedures and the risks that are associated with the study.
  • Participants must be willing to adhere to the protocol and sign the consent form.
  • Participants must be willing to refrain from taking illicit psychoactive substances during the study.
  • Participants must be willing to drink only alcohol-free liquids and no coffee, black or green tea, or energy drink after midnight of the evening before the study session, as well as during the study day.
Show all 10Show fewer
  • Participants must be willing not to drive a traffic vehicle or to operate machines within 48 h after substance administration.
  • Women of childbearing potential must have a negative pregnancy test at the beginning of the study. Pregnancy tests are repeated before each study session.
  • Women of childbearing potential must be willing to use double-barrier birth control.
  • Body mass index between 18-29kg/m2

Who cannot join

  • Chronic or acute medical condition, including a history of seizures.
  • Current or previous major psychiatric disorder (e.g. psychotic disorders, mania / hypomania, anxiety disorders).
  • Psychotic or bipolar disorder in first-degree relatives, not including psychotic disorders secondary to an apparent medical reason, e.g. brain injury, dementia, or lesions of the brain.
  • Hypertension (SBP>140/90 mmHg) or hypotension (SBP<85 mmHg)
  • Ilicit substance use (with the exception of cannabis) more than 20 times or any time within the previous two months
  • Pregnant or nursing women.
Show all 11Show fewer
  • Participation in another clinical trial (currently or within the last 30 days).
  • Use of medications that may interfere with the effects of the study medications (any psychiatric medications and any medication with known to interact with the study substances).
  • Tobacco smoking (>10 cigarettes/day).
  • Consumption of alcoholic drinks (>20 drinks / week).
  • Body weigt < 45 kg.

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • University Hospital Basel

    Basel

Other trials in Switzerland

About this study

4-bromo-2,5-dimethoxyphenethylamine (2C-B) is a psychoactive substance with reportedly similar acute effects to both the prototypical empathogen 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy) and the classic psychedelic substance psilocybin (contained in "magic, hallucinogenic mushrooms"). Pharmacologically, MDMA mainly releases serotonin (5-HT) via the serotonin transporter (SERT) and psilocybin mainly acts as direct agonist at 5-HT2A receptors. 2C-B interacts with both the 5-HT2A receptor and SERT which is in line with its reported mixed effects profile. However, scientific studies are lacking. There is an increased interest in psychiatric research on the therapeutic properties of MDMA and psilocybin and also on mixed empathogenic-psychedelic substances.

Read the detailed description

2C-B is a phenethylamine and belongs to the so-called 2C drugs, a group of novel psychoactive substances (NPS) with some structural similarity to the classic psychedelic mescaline. 2C-B is relatively widely used as recreational substance often replacing or mimicking classic substances such as LSD or MDMA. 2C-B also ranks high among the substances found as substitutes or adulterants of tablets sold as MDMA or Ecstasy. Users report that 2C-B has similar acute effects to MDMA when used at low (5-10 mg) and medium doses (10-25 mg) and more psychedelic effects when used at a high doses (25-40 mg). Additionally, in two open labeled studies the effects have been defined by the researchers as entactogenic (MDMA-like) with psychedelic/hallucinogenic properties when administering 20 mg and on the other hand as psychedelic-psychostimulant like when administering a mean dose of 16 mg (4 used 10 mg, 5 used 15 mg and 7 used 20 mg). Subjective effects peaked at 1-2h and lasted 5h.

The 2C drugs act mainly as agonists on the 5-HT2A receptor very similar to classic psychedelics like LSD or psilocybin. Furthermore, 2C-B may interact with monoaminergic systems more similar to MDMA and may share some empathogenic or even stimulant-type actions. 2C-B also inhibits the SERT similar to MDMA, however, only at low potency in vitro. Thus, taken together, the pharmacology of 2C-B in vitro is somewhat inconclusive but would be consistent with both MDMA- and psychedelic-type actions in vivo in humans. Increases in blood pressure and heart rate are moderate and regarded as lower than those of MDMA. No severe cases were observed. The safety profile of 2C-B is considered to be similar to MDMA.

Psilocybin is a classic serotonergic psychedelic. Psilocybin is a prodrug which is activated to psilocin within the body. The psychoactive action of psilocin primarily involves an interaction with the serotonin 5-HT2A receptor. Currently, psilocybin is the most investigated psychedelic substance among the classic psychedelics. In particular, there are high hopes of using psilocybin in patients with treatment resistant major depression and pharmaceutical companies are currently conducting phase III studies.

MDMA is an amphetamine derivative which, unlike prototypical amphetamines, predominantly enhances serotonergic neurotransmission via release of 5-HT through the SERT and it less potently also releases dopamine and norepinephrine through the dopamine transporter (DAT) and norepinephrine transporter (NET), respectively. Furthermore, MDMA is known to trigger oxytocin release which may contribute to its effects to increase trust, prosociality, and enhanced empathy and is therefore referred to as an "entactogen" or "empathogen". Being granted as a "breakthrough therapy" by the FDA, MDMA is currently investigated in substance-assisted psychotherapy for treatment of PTSD.

By using a placebo-controlled double-blind cross-over design the study will provide insight into the effects profiles of recreationally used psychoactive substances relevant for psychiatric research. Therefore the study will compare the acute subjective, physiological and endocrine effects of low (10 mg), medium (20 mg) and high (30 mg) doses of 2C-B with standard doses of MDMA (125 mg) and psilocybin (25 mg) in healthy subjects.

Finally, the study will also allow to newly directly compare MDMA and psilocybin effects at representative doses and within the same subjects which will provide for a better characterization of these substances increasingly used in psychiatric research.

Conditions
Healthy
Being tested
4-bromo-2,5-dimethoxyphenethylamine (10 mg), 4-bromo-2,5-dimethoxyphenethylamine (20 mg), 4-bromo-2,5-dimethoxyphenethylamine (30 mg), 3,4-methylenedioxymethamphetamine, Psilocybin

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 4-bromo-2,5-dimethoxyphenethylamine (10 mg)Drug

    Also called 2C-B

    A low dose of 10 mg 2C-B will be administered.

  • 4-bromo-2,5-dimethoxyphenethylamine (20 mg)Drug

    Also called 2C-B

    A medium dose of 20 mg 2C-B will be administered.

  • 4-bromo-2,5-dimethoxyphenethylamine (30 mg)Drug

    Also called 2C-B

    A high dose of 30 mg 2C-B will be administered.

  • 3,4-methylenedioxymethamphetamineDrug

    Also called MDMA

    A moderate dose of 125 mg MDMA will be administered.

  • PsilocybinDrug

    A moderate dose of 25 mg psilocybin will be administered.

  • PlaceboOther

    Placebo (Mannitol)

Study groups in NCT05523401
Study groupRoleWhat they receive
10 mg 2C-BExperimental2C-B (10 mg)
Receives: Drug: 4-bromo-2,5-dimethoxyphenethylamine (10 mg)
20 mg 2C-BExperimental2C-B (20 mg)
Receives: Drug: 4-bromo-2,5-dimethoxyphenethylamine (20 mg)
30 mg 2C-BExperimental2C-B (30 mg)
Receives: Drug: 4-bromo-2,5-dimethoxyphenethylamine (30 mg)
125 mg MDMAActive comparatorMDMA (125 mg)
Receives: Drug: 3,4-methylenedioxymethamphetamine
25 mg PsilocybinActive comparatorPsilocybin (25 mg)
Receives: Drug: Psilocybin
PlaceboPlacebo comparatorPlacebo
Receives: Other: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Acute subjective effects I

    5 Dimensions of Altered States of Consciousness (5D-ASC) consisting of 94 items to be rated on a visual analog scale (0-100 mm), with higher values indicating stronger effects with higher scores representing more intense effects.

    Assessed once at the end of the session, 9h after substance administration.

    Measured: 18 months

Secondary outcomes (18)
  1. Acute subjective effects II

    Visual Analog Scale (VAS) will be repeatedly used to assess subjective alterations in consciousness over time. Scales will be administered 14 times throughout the study day.

    Measured: 18 months

  2. Acute subjective effects III

    The Adjective Mood Rating Scale (AMRS) assesses the occurrence and intensity of 60 moods on a 4-point Likert scale ranging from "not at all" to "extremely". It will administred 4 times throughout the study day.

    Measured: 18 months

  3. Autonomic effects I

    Assessed 15 times on each study day via systolic and diastolic blood pressure.

    Measured: 18 months

  4. Autonomic effects II

    Assessed 15 times on each study day via heart rate.

    Measured: 18 months

  5. Autonomic effects III

    Assessed 15 times on each study day via tympanic body temperature.

    Measured: 18 months

  6. Plasma levels of 2C-B, MDMA, and psilocybin

    Assessed 14 times on each study day via blood samples.

    Measured: 18 months

  7. Plasma levels of oxytocin

    Assessed 4 times on each study day via blood samples.

    Measured: 18 months

  8. Plasma levels of Brain-derived neurotropic factor (BDNF)

    Assessed 4 times on each study day via blood samples.

    Measured: 18 months

  9. Adverse effects

    The list of complaints (LC) consists of 66 items, yielding a global score measuring physical and general discomfort. The LC list is administered before (describing the last 24 h as baseline) and after substance administration at the end of the study day describing the acute adverse effects.

    Measured: 18 months

  10. Urine Recovery

    Urine samples will be collected after 2C-B / psilocybin / MDMA / placebo administration (0- 9h).

    Measured: 18 months

  11. States of Consciousness Questionnaire

    Assesses the emergence and intensity of phenomenons occurring in altered states of consciousness on a 6-point Likert scale ranging from 0 ("not at all") to 5 ("extremely"). The scale will be administered once, 9 h after drug administration.

    Measured: 18 months

  12. Spiritual Realms Questionnaire

    Assesses the spiritual phenomenons elicited by psychedelic substances through 11 main questions to be answered on a total of 65 sub-ordered 100mm visual analog scales. The scale will be administered once, 9 hours after substance administration.

    Measured: 18 months

  13. Psychological Insight Questionnaire

    Assesses the degree of psychological insight caused by a psychedelic experience through 14-items to be answered on a 6-point Likert scale ranging from 0 ("not at all") to 5 ("extremely"). The PIQ will be administered once on each study day, 9 hours after substance administration.

    Measured: 18 months

  14. NEO-Five-Factor-Inventory (NEO-FFI)

    The NEO-FFI is a self-description questionnaire with 60 items for the measurement of the "big five": neuroticism, extraversion, openness, agreeableness, and consciousness. It uses a 5-point Likert scale ranging from "completely disagree" to "fully agree".

    Measured: Baseline

  15. Freiburger Personality Inventory (FPI-R)

    The FPI-R version comprises 138 items and covers 12 dimensions of personality: life satisfaction, social orientation, performance orientation, inhibition, excitability, aggressiveness, stress, physical complaints, health concerns, openness, as well as the secondary factors according to Eysenck's Extraversion and Emotionality (Neuroticism). It uses a 2-point scale ("true" and "not true").

    Measured: Baseline

  16. Saarbrücker Personality Questionnaire (SPF)

    The SPF defines empathy as the "reactions of one individual to the observed experiences of another." It assesses 28- items on a 5-point Likert scale ranging from "Does not describe me well" to "Describes me very well". The measure has 4 subscales (Perspective Taking, Fantasy, Empathic Concern, Personal Distress) each made up of 7 different items.

    Measured: Baseline

  17. HEXACO personality inventory

    The HEXACO personality inventory is a six-dimensional model of human personality with 100 items.The six factors are: Honesty-Humility, Emotionality, Extraversion, Agreeableness, Conscientiousness and Openness to Experience.

    Measured: Baseline

  18. Defense Style Questionnaire (DSQ-40)

    The DSQ-40 can provide scores for 20 individual defenses, and scores for the three factors "mature", "neurotic", and "immature". Each item is evaluated on a scale from 1 to 9, where "1" indicates "completely disagree" and "9" indicates "fully agree".

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Aug 2022
  2. Study start16 Aug 2023
  3. Primary completion20 Oct 2024
  4. Study completion5 Nov 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
6-period random order, placebo-controlled, double-blind, cross-over study with five active substance conditions and placebo: 1\. 2C-B (10 mg), 2. 2C-B (20 mg), 3. 2C-B (30 mg), 4. MDMA (125 mg), 5. Psilocybin (25 mg), 6. Placebo
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
24 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05523401
Sponsor's protocol ID
BASEC 2022-00355
Acronym
2C-B
Status last verified
Feb 2025
First submitted
29 Aug 2022
Last updated
5 Mar 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Arikci D, Borgulya J, Straumann I, Vizeli P, Luethi D, Thomann J, Rudin D, Vukalovic I, Eckert A, Liechti ME, Holze F. Acute dose-dependent effects of 4-bromo-2,5-dimethoxyphenethylamine (2C-B) compared with 3,4-methylenedioxymethamphetamine (MDMA) and psilocybin in a double-blind, placebo-controlled study in healthy participants. Neuropsychopharmacology. 2026 Jul;51(8):1511-1518. doi: 10.1038/s41386-026-02428-9. Epub 2026 Apr 28.

    PubMed 42049943

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing 4-bromo-2,5-dimethoxyphenethylamine (10 mg), 4-bromo-2,5-dimethoxyphenethylamine (20 mg) and 4-bromo-2,5-dimethoxyphenethylamine (30 mg) in people with Healthy, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Acute subjective effects I (time frame: 18 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05523401, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Mar 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in