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Completed

NCT Number: NCT02720263

A Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ASP4345 in Patients With Schizophrenia

The purpose of this study is to evaluate the safety and tolerability of multiple ascending oral doses of ASP4345 in patients with schizophrenia. In addition, this study will evaluate the pharmacokinetics of multiple ascending oral doses of ASP4345 in patients with schizophrenia.

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Key information

Conditions

Schizophrenia Mental Disorders Schizophrenia Spectrum and Other Psychotic Disorders

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Site US10001

Glendale, California, 91206, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient has a diagnosis of schizophrenia or schizoaffective disorder according to the Diagnostic and Statistical Manual of Mental Disorders, 5th edition criteria.
  • A patient is considered operationally stable if the patient has a low to moderate positive symptoms score and moderate negative symptom score on the Positive and Negative Syndrome Scale (PANSS): No more than moderate rating on more than 2 PANSS items P1, P2, P3, P5, P6 (positive symptom section); No more than moderate severity rating for the negative items, N1, N2, N3, N4, N5, N6, N7 (negative symptom section); total PANSS score no more than 80.
  • Patient must be in ongoing maintenance antipsychotic therapy other than clozapine (oral or depot), on a stable (≤ 25% change in dose) medication treatment regimen (approved oral or depot formulations of risperidone, quetiapine, olanzapine, ziprasidone, brexpiprazole, aripiprazole, paliperidone or lurasidone) for ≥ 2 months for oral formulations or ≥ 3 months for depot formulations prior to screening, including concomitant psychotropic medications, such as, trazodone and zolpidem for sleep.
  • Patient has a body mass index (BMI) range of 18.5 to 40.0 kg/m2, inclusive, and weighs at least 50 kg at screening.
  • Female patient must be of nonchildbearing potential:
  • Postmenopausal (defined as at least 1 year without any menses) prior to screening, or
  • Documented surgically sterile (at least 1 month prior to screening defined as hysterectomy, bilateral salpingectomy and/or bilateral oophorectomy)
  • Female patient must not donate ova starting at screening and throughout the study period, and for 28 days after the final study drug administration.
  • Male patient and their female spouse/partners who are of childbearing potential must be using 2 forms of highly effective birth control† (1 of which must be a barrier method‡) starting at screening and continue throughout the study period and for 90 days after the final study drug administration.

†Highly effective forms of birth control include:

  • Consistent and correct usage of established oral contraception
  • Injected or implanted hormonal methods of contraception
  • Established intrauterine device or intrauterine system
  • Bilateral tubal ligation
  • Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments and complies with the preferred and usual lifestyle of the patient.

‡Barrier methods of birth control include:

  • Condom with spermicidal foam/gel/film/cream/suppository
  • Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository
  • Male patient must not donate sperm starting at screening and throughout the study period and for 90 days after the final study drug administration.
  • Patient agrees not to participate in another interventional study while participating in the present study, defined as signing the informed consent form until the end of study visit (ESV).
  • Patient has a negative urine drug screen for drugs of abuse at screening and check in.

Exclusion criteria

  • Female patient who has been pregnant within 6 months prior to screening assessment or breastfeeding within 3 months prior to screening.
  • Patient has a known or suspected hypersensitivity to ASP4345 or any components of the formulation used.
  • Patient has had previous exposure with ASP4345.
  • Patient has a history of suicide attempt or suicidal behavior within 2 years prior to screening. Any suicidal ideation that meets criteria at a level of 4 or 5 by using C-SSRS within the last 3 months or who is at significant risk to commit suicide at screening or at admission to the clinical unit (day 2) will be excluded.
  • Patient has any clinically significant liver chemistry test result aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), gamma glutamyl transferase, total bilirubin (TBL) or a result > than 1.5 times above the ULN at screening or at admission to the clinical unit (day 2). In such a case, the assessment may be repeated once.
  • Patient has any history of allergic conditions deemed clinically significant.
  • Patient has any history or evidence of any clinically significant cardiovascular, gastrointestinal endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric (other than schizophrenia or schizoaffective disorder), renal and/or other major disease or malignancy. Patient has any condition, which, makes the patient unsuitable for clinical study participation.
  • Patient has been diagnosed with moderate or severe tardive dyskinesia, bipolar disorder, major depressive disorder, personality disorders, neuroleptic malignancy syndrome or anxiety disorder.
  • Patient has/had febrile illness or symptomatic, viral, bacterial (including upper respiratory infection) or fungal (noncutaneous) infection within 1 week prior to admission to the clinical unit (day 2).
  • Patient has any clinically significant abnormality at screening or at admission to the clinical unit (day 2).
  • Patient has a mean pulse < 40 or > 100 bpm; mean systolic blood pressure (SBP) > 160 mmHg; mean diastolic blood pressure (DBP) > 90 mmHg (vital signs measurements taken in triplicate after patient has been resting in supine position for 5 minutes; pulse will be measured automatically) at screening or at admission to the clinical unit (day 2). If the mean blood pressure exceeds the limits above, 1 additional triplicate can be taken on day 2.
  • Patient has a mean QTcF > 440 msec (for male patients) and > 460 msec (for female patients) at screening or at admission to the clinical unit (day 2). If the mean QTcF exceeds the limits above, 1 additional triplicate ECG can be taken on day 2.
  • Patient uses any prescribed or nonprescribed drugs (including vitamins, natural and herbal remedies, e.g., Valerian) in the 2 weeks prior to study drug administration, except for:
  • Approved antipsychotics (risperidone, quetiapine, olanzapine, ziprasidone, brexpiprazole, aripiprazole, paliperidone or lurasidone), or
  • Approved intermittent use of trazodone or zolpidem (no less than 12 hours prior to dosing), or
  • Approved use of concomitant medication for the treatment of hypertension, hyperlipidemia or diabetes mellitus, or
  • Occasional use of acetaminophen (up to 2 g/day).
  • Patient has a history of consuming more than 14 units of alcoholic beverages per week within 6 months prior to screening or has a history of alcoholism or drug/chemical/substance abuse within past 2 years prior to screening (Note: 1 unit = 12 ounces of beer, 4 ounces of wine or 1 ounce of spirits/hard liquor) or the patient tests positive for alcohol or drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine and opiates) at screening or at admission to the clinical unit (day 2). A patient with a positive result for benzodiazepines may be included in this clinical study, if the result can be explained by the use of permitted concomitant medication.
  • Patient has used any strong CYP3A inhibitors (e.g., but not limited to: boceprevir, clarithromycin, conivaptan, indinavir, itraconazole, ketoconazole, lopinavir/ritonavir, mibefradil, nefazodone, nelfinavir, posaconazole, ritonavir, saquinavir, telaprevir, telithromycin, voriconazole) and/or has consumed grapefruit, grapefruit containing products, Seville orange or Seville orange containing products within 72 hours prior to admission to the clinical unit (day 2).
  • Patient has used any strong or moderate CYP2D6 inhibitors (e.g., but not limited to: bupropion, fluoxetine, paroxetine, quinidine, cinacalcet, duloxetine, terbinafine) within 72 hours prior to admission to the clinical unit (day 2).
  • Patient regularly uses any inducer of metabolism (e.g., but not limited to: barbiturates, rifampin, St. John's Wort) in the 1 month prior to admission to the clinical unit (day 2).
  • Patient has used any drugs of abuse within 3 months prior to admission to the clinical unit (day 2).
  • Patient has had significant blood loss, donated 1 unit (450 mL) of blood or more, or received a transfusion of any blood or blood products within 60 days or donated plasma within 7 days prior to admission to the clinical unit (day 2).
  • Patient has a positive serology test for hepatitis B surface antigen (HBsAg), hepatitis A virus (HAV) antibodies (immunoglobulin M [IgM]), hepatitis C virus (HCV) antibodies, or human immunodeficiency virus (HIV) antibodies type 1 or 2 at screening.
  • Patient has participated in any clinical study or has been treated with any investigational drugs within 28 days or 5 half lives whichever is longer, prior to screening.
  • Patient is an employee of the Astellas Group or Contract Research Organization (CRO) involved in the clinical study.
  • Patient who has had electroconvulsive therapy within the 6 months prior to screening.
  • Patient has a history of seizures or of a condition with risk of seizures; as an exception, a history of 1 febrile seizure in childhood will not exclude a patient.
  • Patient has a history of head injury with clinically significant sequelae.
  • Patient experienced an acute exacerbation of schizophrenia requiring hospitalization within the last 3 months.
  • Patient experienced an acute exacerbation of schizophrenia requiring increase in antipsychotic medication (with reference to drug or dose) within the last 4 weeks.
  • Patient has hearing loss, is unable to detect 1000 Hz tones presented at 40 dB.
  • Patient has a hairstyle that would interfere with electroencephalogram (EEG) recording quality.
  • Patient has a history of spine surgery (with intact dura mater) in the past year and/or a history of brain and/or spinal cord injury.

Treatment and study plan

ASP4345

Drug

Oral

Matching Placebo

Drug

Oral

Primary outcomes

  1. Safety and tolerability assessed as nature, frequency and severity of adverse events

    Time frame: Up to Day 21

  2. Change from baseline in supine blood pressure as a measure of safety and tolerability

    Time frame: Baseline and Day 21

  3. Change from baseline in pulse as a measure of safety and tolerability

    Time frame: Baseline and Day 21

  4. Change from baseline in oral body temperature as a measure of safety and tolerability

    Time frame: Baseline and Day 21

  5. Safety and tolerability assessed by an orthostatic challenge test

    Time frame: Up to Day 14

    Incidence of positive orthostatic challenge tests will be summarized.

  6. Number of participants with abnormal laboratory values and/or adverse events related to treatment

    Time frame: Up to Day 21

    Clinical laboratory tests include hematology, biochemistry and urinalysis.

  7. Safety and tolerability assessed by routine 12-lead electrocardiogram (ECG)

    Time frame: Up to Day 18

    The overall interpretation of 12-lead electrocardiogram (ECG) results (normal, abnormal not clinically significant and abnormal clinically significant) will be summarized.

  8. Safety and tolerability assessed by continuous 12-lead ECG recording

    Time frame: Up to Day 14

    ECGs will be collected using a 12-lead ECG continuous monitoring system which records continuous digital data.

  9. Safety and tolerability assessed by abuse liability using an Addiction Research Center Inventory (ARCI-49)

    Time frame: Up to Day 17

    ARCI-49 is a 49-item short form standardized questionnaire for abuse potential liability.

  10. Safety and tolerability assessed by Columbia-Suicide Severity Rating Scale (C-SSRS)

    Time frame: Up to Day 18

    The C-SSRS is a scale that assesses the full spectrum of suicidality: suicidal ideation, intensity of ideation, suicidal behaviors and actual attempts.

  11. Safety and tolerability assessed by Bond-Lader Visual Analog Scale (VAS)

    Time frame: Up to Day 17

    The VAS will be used to rate patients' feelings in terms of 16 dimensions. The dimensions will be presented as 100 mm lines, the 2 extremes of the emotion (i.e., alert - drowsy) written at each end.

  12. Safety and tolerability assessed by metabolic syndrome: weight circumference

    Time frame: Up to Day 14

  13. Safety and tolerability assessed by metabolic syndrome: cholesterol

    Time frame: Up to Day 21

  14. Safety and tolerability assessed by metabolic syndrome: triglycerides

    Time frame: Up to Day 21

  15. Safety and tolerability assessed by metabolic syndrome: glucose level

    Time frame: Up to Day 21

  16. Safety and tolerability assessed by weight

    Time frame: Up to Day 14

  17. Safety and tolerability assessed by movement disorder: Abnormal Involuntary Movement Scale (AIMS)

    Time frame: Up to Day 14

    The AIMS is a checklist and uses a 5-point rating scale for recording scores for 7 body areas: face, lips, jaw, tongue, upper extremities, lower extremities and trunk.

  18. Safety and tolerability assessed by movement disorder: Simpson Angus Scale (SAS)

    Time frame: Up to Day 14

    The SAS is a 10-item scale used to rate adverse neurological effects of antipsychotic medications more broadly. Each item is rated from 0 to 4 and a total score will be obtained.

  19. Safety and tolerability assessed by movement disorder: Barnes Akathisia Rating Scale (BARS)

    Time frame: Up to Day 14

    The BARS is a rating scale used to assess the severity of drug-induced akathisia.

  20. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): tlag

    Time frame: Day 1

    Time prior to the time corresponding to the first measurable (nonzero) concentration (tlag)

  21. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): tmax

    Time frame: Day 1 and Day 14

    Time of maximum concentration (tmax)

  22. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): Cmax

    Time frame: Day 1 and Day 14

    Maximum concentration (Cmax)

  23. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): AUCtau

    Time frame: Day 1 and Day 14

    Area under the concentration-time curve from the time of dosing to the start of the next dosing interval (AUCtau)

  24. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): Ctrough

    Time frame: Days 2 through 14

    Concentration immediately prior to dosing at multiple dosing (Ctrough)

  25. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): t1/2

    Time frame: Day 14

    Terminal elimination half-life (t1/2)

  26. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): MRTinf

    Time frame: Day 14

    Mean residence time extrapolated to time infinity (MRTinf)

  27. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): terminal elimination rate constant

    Time frame: Day 14

  28. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): Vz/F

    Time frame: Day 14

    Apparent volume of distribution during the terminal elimination phase after single extravascular dosing (Vz/F)

  29. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): CL/F

    Time frame: Day 14

    Apparent total systemic clearance after extravascular dosing (CL/F)

  30. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): Rac(AUC)

    Time frame: Day 14

    Accumulation index area under the concentration-time curve (Rac(AUC))

  31. Pharmacokinetics of ASP4345 and its metabolites, if necessary (plasma): PTR

    Time frame: Day 14

    Peak trough ratio (PTR)

  32. Pharmacokinetics of ASP4345 and its metabolites, if necessary (urine): Aetau

    Time frame: Day 14

    Cumulative amount of study drug excreted into urine from the time of dosing to the start of the next dosing interval (Aetau)

  33. Pharmacokinetics of ASP4345 and its metabolites, if necessary (urine): Aetau%

    Time frame: Day 14

    Percentage of study drug dose excreted into urine from the time of dosing to the start of the next dosing interval (Aetau%)

  34. Pharmacokinetics of ASP4345 and its metabolites, if necessary (urine): CLR

    Time frame: Day 14

    Renal clearance (CLR)

Sponsors and collaborators

Lead sponsor

Astellas Pharma Global Development, Inc.

Industry

Registry information

Official study title

A Phase 1 Multiple Ascending Oral Dose Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ASP4345 in Patients With Schizophrenia

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Mar 25, 2016
Registry last updated
Oct 31, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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