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Clinical Trials in the USA / NCT05025605
Recruiting Phase 1

Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder

NCT05025605 · tracked via the Priya Life Science USA tracker
Sponsor
BioXcel Therapeutics Inc
Phase
Phase 1
Started
2021-08-27
Last updated
2026-08-11

Condition(s) studied

SchizophreniaSchizo-Affective DisorderSchizophreniform; SchizophrenicBipolar Disorder IBipolar Disorder II

Investigational drug(s) / intervention(s)

BXCL501 80 MicrogramsPlacebo FilmBXCL501 120 MicrogramsBXCL501 60 Micrograms

BXCL501 80 Micrograms: Sublingual film containing 80 Micrograms BXCL501

Placebo Film: Matching Sublingual Placebo film

BXCL501 120 Micrograms: Sublingual film containing 120 Micrograms BXCL501

BXCL501 60 Micrograms: Sublingual film containing 60 Micrograms BXCL501 Europe Only

Study summary

This is a study of the efficacy and safety of BXCL501 in children and adolescents with acute agitation and either bipolar disorder or schizophrenia.

Eligibility

Sex
ALL
Min age
10 Years
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: 1. Male and female subjects between the ages of 10-17 years, inclusive, with bipolar disorder (DSM-5 criteria) and 13-17 years, inclusive, in subjects with schizophrenia (DSM-5 criteria). 2. Patients who are judged to be clinically agitated at Screening and Baseline with a total score of ≥14 on the 5 items comprising the PANSS Excited Component (PEC). 3. Patients who have a score of ≥ 4 on at least 1 of the 5 items on the PEC at Baseline. 4. Participants who agree to use a medically acceptable and effective birth control method Exclusion Criteria: 1. Patients with agitation caused by acute intoxication, including alcohol or drugs of abuse (with the exception of THC) during urine screening. 2. Use of benzodiazepines or other hypnotics or oral or short-acting intramuscular antipsychotic drugs in the 4 hours before study treatment. 3. Patients who are judged to be at significant risk of suicide. 4. Patients with serious or unstable medical illnesses. 5. Patients who have received an investigational drug within 30 days prior to the current agitation episode. 6. Patients who are considered by the investigator, for any reason, to be an unsuitable candidate for receiving the study drug.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
BioXcel Clinical Research Site Anaheim California Recruiting
Bioxcel Clinical Research Site Hialeah Florida Recruiting
BioXcel Clinical Research Site Atlanta Georgia Completed
Bioxcel Clinical Research Site Decatur Georgia Recruiting
BioXcel Clinical Research Site DeSoto Texas Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05025605 on ClinicalTrials.gov ↗ ← All trials in the USA