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NCT07484204RecruitingPhase 1

Evaluate Pharmacokinetics, Safety, and Tolerability of AX251 LAI in Patients With Schizophrenia

An Open-label, Multicenter Study to Determine the Pharmacokinetics, Safety, and Tolerability of AX251 Long-Acting Injectable (LAI) Administered as a Single Dose in Patients With Schizophrenia

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

The purpose of this study is to assess the pharmacokinetics (PK), safety, and tolerability of AX251 long-acting injectable (LAI) administered as a single dose in patients with schizophrenia. The study will include sequential dose-escalation cohorts to evaluate different dose levels of AX251 LAI.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
48 (estimated)
First submitted
16 Mar 2026
Start date
14 Sept 2026
Primary completion date
31 Jul 2028
Lead sponsor
Anxo Pharmaceutical Co., Ltd.
NCT number
NCT07484204

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 48
  • From 14 Sept 2026 to the primary completion date, 31 Jul 2028
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Substance use disorder (including alcohol or benzodiazepines) within 180 days prior to screening, excluding caffeine and tobacco.
  • Failure to complete required washout period (≥5 half-lives) for prohibited medications before administration of AX251 LAI.
  • Current treatment with other antipsychotic long-acting injectable (LAI) therapies.
  • Electroconvulsive therapy within 60 days prior to screening.

Other illness

  • Diagnosis of psychiatric disorders other than schizophrenia according to DSM-5-TR (e.g., schizoaffective disorder, major depressive disorder, bipolar disorder, generalized anxiety disorder, obsessive-compulsive disorder, post-traumatic stress disorder, dementia, mild neurocognitive disorder, or personality disorders), except caffeine- or tobacco-related disorders.
  • History of neuroleptic malignant syndrome, seizure disorder, or clinically significant tardive dyskinesia, akathisia, or extrapyramidal symptoms.
  • Clinically significant cardiovascular, hematologic, metabolic, hepatic, renal, immunologic, or neurological disease that may interfere with study participation.
  • Severe hepatic impairment (Child-Pugh Class C) at screening.
  • Uncontrolled hypertension.
  • Severe renal impairment (estimated glomerular filtration rate \<30 mL/min).
  • History of syncope or significant orthostatic hypotension at screening.

Other

  • Clinically significant electrocardiogram abnormalities at screening.
  • Acute psychosis posing imminent risk to self or others.
  • Acute relapse of schizophrenia at screening.

Who the study is looking for

  • Male or female subjects aged 18 to 65 years (inclusive).
  • clinical diagnosis of schizophrenia per the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) (or later) criteria, at screening.
  • Body Mass Index (BMI) 18.5-35.0 kg/m² at screening.
  • Clinical Global Impression-Severity (CGI-S) score ≤4 at screening.
  • Positive and Negative Syndrome Scale (PANSS) total score ≤75 at screening.
  • Clinically stable schizophrenia on current antipsychotic medication other than cariprazine for at least 3 months prior to screening.
  • Subjects must not be taking more than two antipsychotic medications.
  • Able to remain at the study site for 7 days following AX251 LAI injection.
  • Judged by the investigator to be physically and mentally able to participate in the study based on clinical evaluation, physical examination, electrocardiogram (ECG), and laboratory assessments.
  • Willing and able to comply with study procedures.
  • Agrees to use protocol-defined contraception during the study.
  • Previous tolerability to oral cariprazine (1.5-6 mg) or willingness to undergo a short oral tolerability test (2-7 days) followed by washout before study drug administration.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Health Hospital
Coordinator of this site? Confirm its status
AhmedabadIndiaRecruiting
DHS Multispeciality Hospital
Coordinator of this site? Confirm its status
AhmedabadIndiaRecruiting
Divine Multispeciality Hospital
Coordinator of this site? Confirm its status
GandhinagarIndiaRecruiting
Ratandeep Multispeciality Hospital
Coordinator of this site? Confirm its status
NagarIndiaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.