Recruiting PHASE1 Schizophrenia

Tests treatment safety and results for Schizophrenia

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

ClinicalTrials.gov ID: NCT05025605

What this study is testing

What is BXCL501 80 Micrograms?

BXCL501 80 Micrograms is an investigational medicine, being studied as a potential treatment for schizophrenia.

Also referred to as Dexmedetomidine.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This is a study of the efficacy and safety of BXCL501 in children and adolescents with acute agitation and either bipolar disorder or schizophrenia.
  • Phase 1: an early, usually small safety study
  • You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 10 to 17

You may be able to join if

  • Male and female people between the ages of 10-17 years, inclusive, with bipolar disorder (DSM-5 criteria) and 13-17 years, inclusive, in people with...
  • 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...
  • Patients who have a score of ≥ 4 on at least 1 of the 5 items on the PEC at Baseline.
  • Participants who agree to use a medically acceptable and effective birth control method

You likely can't join if

  • Patients with agitation caused by acute intoxication, including alcohol or drugs of abuse (with the exception of THC) during urine screening.
  • Use of benzodiazepines or other hypnotics or oral or short-acting intramuscular antipsychotic drugs in the 4 hours before study treatment.
  • Patients who are judged to be at significant risk of suicide.
  • Patients with serious or unstable medical illnesses.
  • Patients who have received an investigational drug within 30 days prior to the current agitation episode.
  • Patients who are considered by the investigator, for any reason, to be an unsuitable candidate for receiving the study drug.

The study team makes the final eligibility decision.

Where it's taking place

  • Anaheim, California, United States
  • Hialeah, Florida, United States
  • Atlanta, Georgia, United States
  • Decatur, Georgia, United States
  • DeSoto, Texas, United States

Compensation & support

Compensation mentioned.

ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.

Questions & answers

Do participants get paid in this trial?

This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 10 years to 17 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Anaheim, California, United States; Hialeah, Florida, United States; Atlanta, Georgia, United States; Decatur, Georgia, United States; DeSoto, Texas, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.