Sub-Lingual Dexmedetomidine in Agitation Associated With Schizophrenia

Completed · Phase 1 · Has a placebo group

Conditions studied: Agitation, Schizophrenia

In brief

This is a two-stage adaptive Phase Ib trial design, that will identify two doses (lowest dose with clinical benefit and highest safe dose) in a first stage and better evaluate safety, tolerability and variability of effect in the second stage.

Key facts

Study ID

NCT04010305

Run by

BioXcel Therapeutics Inc

People needed

135

Starts

2019-05-22

Expected to finish

2019-07-31

Last updated by the study team

2023-02-08

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female patients between the ages of 18 to 65 years, inclusive.
• Patients who have met Diagnostic and Statistical Manual (DSM) -5 criteria for schizophrenia, schizoaffective, or schizophreniform disorder.
• Patients who are judged to be clinically agitated at Baseline with a total score of ≥ 14 on the 5 items (poor impulse control, tension, hostility, uncooperativeness, and excitement) comprising the PANSS Excited Component (PEC).
• Patients who have a score of ≥ 4 on at least 1 of the 5 items on the PEC.
• Patients who read, understand and provide written informed consent.
• Patients who are in good general health prior to study participation as determined by a detailed medical history, physical examination, 12-lead ECG, blood chemistry profile, hematology, urinalysis and in the opinion of the Principal Investigator.
• Female participants, if of child-bearing potential and sexually active, and male participants, if sexually active with a partner of child-bearing potential, who agree to use a medically acceptable and effective birth control method throughout the study and for one week following the end of the study. Medically acceptable methods of contraception that may be used by the participant and/or his/her partner include abstinence, birth control pills or patches, diaphragm with spermicide, intrauterine device (IUD), condom with foam or spermicide, vaginal spermicidal suppository, surgical sterilization and progestin implant or injection. Prohibited methods include: the rhythm method, withdrawal, condoms alone, or diaphragm alone.

You may not qualify if…

• Patients with agitation caused by acute intoxication, including positive identification of alcohol by breathalyzer or non-prescription drugs (with the exception of THC) during urine screening.
• Patients treated within 4 hours prior to study drug administration with benzodiazepines, other hypnotics or oral or short-acting intramuscular antipsychotics.
• Treatment with alpha-1 noradrenergic blockers (terazosin, doxazosin, tamsulosin, and alfuzosin, and prazosin) or other prohibited medications.
• Patients with significant risk of suicide or homicide per the investigator's assessment, or any suicidal behavior in last 6 months prior to screening.
• Female patients who have a positive pregnancy test at screening or are breastfeeding.
• Patients who have hydrocephalus, seizure disorder, or history of significant head trauma, stroke, transient ischemic attack, subarachnoid bleeding, brain tumor, encephalopathy, meningitis, Parkinson's disease or focal neurological findings.
• History of syncope or other syncopal attacks, current evidence of hypovolemia, orthostatic hypotension, a screening heart rate of < 55 beats per minutes or systolic blood pressure <110 mmHg or diastolic BP <70 mmHg.
• Patients with laboratory or ECG abnormalities considered clinically significant by the investigator or qualified designee [Advanced heart block (second-degree or above atrioventricular block without pacemaker), diagnosis of Sick sinus syndrome] that would have clinical implications for the patient's participation in the study.
• Patients with serious or unstable medical illnesses. These include current hepatic (moderate-severe hepatic impairment), renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease, congestive heart failure), endocrinologic, or hematologic disease.
• Patients who have received an investigational drug within 30 days prior to the current agitation episode.
• Patients who are unable to use the sublingual film or considered by the investigator, for any reason, to be an unsuitable candidate for receiving dexmedetomidine; e.g. patients with a history of allergic reactions to dexmedetomidine.

Where it is running

• BioXcel Clinical Research Site — Little Rock, Arkansas, United States
• BioXcel Clinical Research Site — Cerritos, California, United States
• BioXcel Clinical Research Site — Lemon Grove, California, United States
• BioXcel Clinical Research Site — Long Beach, California, United States
• BioXcel Clinical Research Site — Orange, California, United States
• BioXcel Clinical Research Site — Miami Lakes, Florida, United States
• BioXcel Clinical Research Site — Atlanta, Georgia, United States
• BioXcel Clinical Research Site — Gaithersburg, Maryland, United States
• BioXcel Clinical Research Site — Flowood, Mississippi, United States
• BioXcel Clinical Research Site — Berlin, New Jersey, United States
• BioXcel Clinical Research Site — Austin, Texas, United States
• BioXcel Clinical Research Site — Richardson, Texas, United States

Full record on ClinicalTrials.gov

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