Safety and Tolerability Study of Single-dose Administration of Brexpiprazole in Adult Subjects With Schizophrenia

Schizophrenia Clinical Trial

Official title:

A Phase 1, Two-part, Open-label, Randomized, Exploratory and Single Ascending Dose, Parallel Arm Trial to Determine the Pharmacokinetics, Safety, and Tolerability of Brexpiprazole Long-acting Injectable Administered Subcutaneously or Intramuscularly in Adult Subjects With Schizophrenia

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02968121
• Other study ID #: 331-201-00033
• Status: Terminated
• Phase: Phase 1
• First received: November 2, 2016
• Last updated: January 10, 2018
• Start date: January 2017
• Est. completion date: December 14, 2017

Study information

• Verified date: January 2018
• Source: Otsuka Pharmaceutical Development & Commercialization, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To determine the pharmacokinetics, safety and tolerability of brexpiprazole administered subcutaneously or intramuscularly in adults with schizophrenia.

Description:

This trial is designed to assess the pharmacokinetics, safety and tolerability of brexpiprazole in the treatment of subjects with schizophrenia. The trial will consist of two parts across 13-36 months. The trial population will include approximately 110 male & female subjects between 18 and 64 years of age (inclusive) with a diagnosis of schizophrenia as defined by DSM-V criteria.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 22
• Est. completion date: December 14, 2017
• Est. primary completion date: December 14, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

• Males and females between 18 and 64 years of age, inclusive, at the screening visit with a diagnosis of schizophrenia as defined by DSM-V criteria.

• Body mass index between 18 and 35 kg/m^2 at the screening visit.

• Good physical health as determined by no clinically significant deviation from normal.

• Ability to provide informed consent and/or consent obtained from a legally acceptable representative (as required by IRB), prior to the initiation of any protocol-required procedures.

• Male and female subjects who are surgically sterile, female subjects who have been postmenopausal for at least 12 consecutive months prior to the screening visit, or male subjects/female subjects (of childbearing potential) who agree to remain abstinent or to practice 2 of the approved birth control methods from the screening visit and for at least 150 days after the dose of IMP for a female subject or 180 days after the dose of IMP for a male subject.

Exclusion Criteria:

• Subjects who have:

• Met DSM-V criteria for substance use disorder within the past 180 days; including alcohol and benzodiazepines, excluding caffeine/nicotine.

• A positive drug screen for drugs of abuse (excluding stimulants, other prescribed medications, and marijuana [if in investigator's documented opinion the subject does not meet DSM-V criteria for substance use disorder]).

• Use of more than 1 psychotropic medication at the screening or baseline visit, except for oral brexpiprazole administered during the brexpiprazole tolerability testing (if applicable) and current oral antipsychotic medication.

• Use of varenicline beyond screening.

• Subjects who have participated in any clinical trial involving a psychotropic medication within 1 month prior to the administration of IMP or 5 half-lives from last IMP administration whichever is longer.

• Subjects who have a significant risk of committing suicide based on history, routine psychiatric status examination, investigator's judgment, or who have an answer of "yes" on questions 4 or 5 on the Baseline Version of the C-SSRS.

• Subjects currently in an acute relapse of schizophrenia as assessed by the investigator.

• Subjects with a current DSM-V diagnosis other than schizophrenia. Also, subjects with borderline, paranoid, histrionic, schizotypal, schizoid, or antisocial personality disorder.

Related Conditions & MeSH terms

• Schizophrenia

Intervention

Drug:
• Brexpiprazole, OPDC-34712

Locations

Country	Name	City	State
United States	Collaborative Neuro Science (CNS)	Garden Grove	California
United States	CNRI	San Diego	California

Sponsors (2)

Lead Sponsor	Collaborator
Otsuka Pharmaceutical Development & Commercialization, Inc.	H. Lundbeck A/S

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Suicidality via Columbia-Suicide Severity Rating Scale	Baseline version and Since Last Visit version of CSSRS will be completed by trained trial center staff	Part A: Screening to Day 182; Part B: Screening to Day 126
Primary	Number of reported Adverse Events (AE)		Part A: 182 days; Part B: 126 days
Primary	Clinical Laboratory Tests	Hematology, serum chemistry, urinalysis, drug screen, etc. will be performed.	Part A: 182 days; Part B: 126 days
Primary	Change in physical exam results	Investigator or designee will perform complete physical exam and document any clinically significant conditions. Body height and weight will also be measured for BMI calculation and weight will be measured as part of all subsequent physical exams.	Part A: Screening to Day 182; Part B: Screening to Day 126
Primary	Change in Systolic/Diastolic blood pressure from screening to end of study	Heart rate and body temperature will also be obtained prior to PK blood draws and ECG.	Part A: Screening to Day 182; Part B: Screening to Day 126
Primary	ECG Reading	12-lead ECG will be collected in triplicate (5 minutes apart). heart rate, ventricular rate, RR interval, PR interval, QRS duration and QT intervals will be recorded. QTcF and corrected QT interval using Bazett's formula will be calculated.	Part A: 182 days; Part B: 126 days
Primary	Extrapyramidal Symptoms (EPS) Rating Scale	SAS, AIMS & BARS will be assess by trained trial center staff	Part A: 182 days; Part B: 126 days
Primary	Investigator's assessment of injection site	Injection site will be assessed. Injection site will also be inspected for seepage after needle is withdrawn.	Part A: 182 days; Part B: 126 days
Primary	Visual analog scale (VAS) scores for pain reception		Part A: 182 days; Part B: 126 days
Secondary	Maximum peak plasma concentration (Cmax) [Pharmacokinetics]	Samples will also be collected on Days 2, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 25, 28, 35, 42, 49, 56, 63, 70, 77, 84, 98, 112, 126, 154, and 182/ET or until plasma concentrations of brexpiprazole are BLQ, whichever is longer based on monthly PK sampling (samples will be collected between 8 AM and 2 PM on the indicated nondosing day). If a PK blood sample cannot be drawn at the designated time on Day 1, a window of ± 15 minutes for each blood draw is acceptable with the exact time recorded.; PK parameters will be assessed for plasma brexpiprazole and its metabolite(s) including DM-3411.	Day 1 (predose [within 2 hours prior to dosing] and 4, 8 , and 12 hours postdose)
Secondary	Time of Cmax (tmax) [Pharmacokinetics]	Samples will also be collected on Days 2, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 25, 28, 35, 42, 49, 56, 63, 70, 77, 84, 98, 112, 126, 154, and 182/ET or until plasma concentrations of brexpiprazole are BLQ, whichever is longer based on monthly PK sampling (samples will be collected between 8 AM and 2 PM on the indicated nondosing day). If a PK blood sample cannot be drawn at the designated time on Day 1, a window of ± 15 minutes for each blood draw is acceptable with the exact time recorded.; PK parameters will be assessed for plasma brexpiprazole and its metabolite(s) including DM-3411	Day 1 (predose [within 2 hours prior to dosing] and 4, 8 , and 12 hours postdose)
Secondary	Area under the concentration-time curve (AUC) from time zero to time "t" (Last observable concentration; AUCt) [Pharmacokinetics]	Samples will also be collected on Days 2, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 25, 28, 35, 42, 49, 56, 63, 70, 77, 84, 98, 112, 126, 154, and 182/ET or until plasma concentrations of brexpiprazole are BLQ, whichever is longer based on monthly PK sampling (samples will be collected between 8 AM and 2 PM on the indicated nondosing day). If a PK blood sample cannot be drawn at the designated time on Day 1, a window of ± 15 minutes for each blood draw is acceptable with the exact time recorded.; PK parameters will be assessed for plasma brexpiprazole and its metabolite(s) including DM-3411	Day 1 (predose [within 2 hours prior to dosing] and 4, 8 , and 12 hours postdose)
Secondary	AUC from time zero to infinity (AUC8) [Pharmacokinetics]	Samples will also be collected on Days 2, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 25, 28, 35, 42, 49, 56, 63, 70, 77, 84, 98, 112, 126, 154, and 182/ET or until plasma concentrations of brexpiprazole are BLQ, whichever is longer based on monthly PK sampling (samples will be collected between 8 AM and 2 PM on the indicated nondosing day). If a PK blood sample cannot be drawn at the designated time on Day 1, a window of ± 15 minutes for each blood draw is acceptable with the exact time recorded.; PK parameters will be assessed for plasma brexpiprazole and its metabolite(s) including DM-3411	Day 1 (predose [within 2 hours prior to dosing] and 4, 8 , and 12 hours postdose)
Secondary	Terminal-phase elimination half-life (t1/2,z) [Pharmacokinetics]	Samples will also be collected on Days 2, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 25, 28, 35, 42, 49, 56, 63, 70, 77, 84, 98, 112, 126, 154, and 182/ET or until plasma concentrations of brexpiprazole are BLQ, whichever is longer based on monthly PK sampling (samples will be collected between 8 AM and 2 PM on the indicated nondosing day). If a PK blood sample cannot be drawn at the designated time on Day 1, a window of ± 15 minutes for each blood draw is acceptable with the exact time recorded.; PK parameters will be assessed for plasma brexpiprazole and its metabolite(s) including DM-3411	Day 1 (predose [within 2 hours prior to dosing] and 4, 8 , and 12 hours postdose)
Secondary	Apparent clearance of drug from plasma after extravascular administration (CL/F; brexpiprazole only) [Pharmacokinetics]	Samples will also be collected on Days 2, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 25, 28, 35, 42, 49, 56, 63, 70, 77, 84, 98, 112, 126, 154, and 182/ET or until plasma concentrations of brexpiprazole are BLQ, whichever is longer based on monthly PK sampling (samples will be collected between 8 AM and 2 PM on the indicated nondosing day). If a PK blood sample cannot be drawn at the designated time on Day 1, a window of ± 15 minutes for each blood draw is acceptable with the exact time recorded.; PK parameters will be assessed for plasma brexpiprazole and its metabolite(s) including DM-3411	Day 1 (predose [within 2 hours prior to dosing] and 4, 8 , and 12 hours postdose)