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Bioequivalence Study of Cariprazine Capsules 1.5 mg

An Open Label, Balanced, Randomized, Two Treatment, Two Sequence, Two Period, Crossover, Single Dose Oral Bioequivalence Study of Cariprazine Capsules 1.5 mg (Test) of Optimus Pharma Limited, India and CARISPECTM (Cariprazine) Capsules 1.5 mg (Reference) of SUN Pharmaceutical Industries Ltd., in Healthy Adult Human Subjects under Fasting Condition

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041819
Enrollment
46
Registered
2022-04-12
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Cariprazine Capsules 1.5 mg: Cariprazine Capsules 1.5 mg Manufactured by: Optimus Pharma Limited, India Control Intervention1: Carispec (Cariprazine) Capsules 1.5 mg: Carispec (Caripraz

Sponsors

Optimus Pharma Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Volunteers meeting all the following inclusion criteria will be considered for enrolment in the study: 1. Healthy human subjects aged between 18 years and 45 years (both inclusive). 2. Having a Body Mass Index (BMI) between 18.50 and 24.99 kg/m2 (both inclusive). 3. All volunteers must be judged by the Principal or Co-investigator or physician as normal and have no abnormal (clinically significant) findings during screening (medical history and examination, vitals, laboratory evaluations and ECG recording) within 28 days and chest X-Ray evaluation within 12 months prior to period-I dosing of study drug. 4. Normal values in the assessment of depression using Depression Assessment Scale during each period check-in. 5. Subjects are non-smokers and non-alcoholics. 6. Subjects willing to adhere to protocol requirements and provide written informed consent. 7. Females who are a. Childbearing potential practicing an acceptable method of birth control for the duration of the study as judged by the investigator(s), such as condoms, foams, jellies, diaphragm, intrauterine devices (IUD) or abstinence: or b. Post-menopausal for at least 1 year, or c. Surgically sterile (has undergone bilateral tubal ligation, bilateral; oophorectomy or hysterectomy).

Exclusion criteria

Exclusion criteria: Volunteers will be excluded from participation in the study, if they meet any one of the following exclusion criteria 1. Volunteer having known history of hypersensitivity to Cariprazine or to any component of the formulation. 2. History or evidence of Depression, Suicidal Ideation, Suicidal Behavior, and Exacerbation of Mood Disorders. 3. History of Irritable bowel syndrome with pain/discomfort as predominant symptom. 4. History of constipation or chronic constipation and using related drugs. 5. History or suspected with Intestinal obstruction due to tumor, hernia etc, as bowel obstruction disorder. 6. History or evidence of COVID-19 during last 1 month 7. History of loose stools in past 10 days. 8. Any disease or condition which might compromise the hematopoietic, renal, hepatic, endocrine, pulmonary, central nervous, cardiovascular, immunological, dermatological, gastrointestinal, genital or any other body system. 9. Participation in any clinical research study or any bioavailability/bioequivalence study within 90 days prior to first dosing of the present study. 10. Blood donation within 90 days prior to first dosing of the present study. 11. History of difficulty in donating blood or difficulty in accessibility of veins. 12. History or evidence of drug dependence.

Design outcomes

Primary

MeasureTime frame
To compare the rate and extent of absorption of Cariprazine Capsules 1.5 mg of Optimus Pharma Limited, India and CARISPECTM (Cariprazine) Capsules 1.5 mg of SUN Pharmaceutical Industries Ltd., in healthy, adult, human subjects under fasting Condition.Timepoint: NIL

Secondary

MeasureTime frame
To monitor the subject�s safety and tolerability of single dose oral dose of investigational products (IPs).Timepoint: NIL

Countries

India

Contacts

Public ContactVinayak Sargar

Admerus Biosciences Private Limited

Daniel.s@admerus.com04067927777

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026