Bioequivalence Study of Clonazepam 2 Mg Tablets

NCT ID: NCT06834503

Last Updated: 2025-03-10

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE4
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-06-10
• Study Completion Date: 2025-11-01

Brief Summary

Demonstrate the bioequivalence in 1 study, in fasting condition of two formulations of clonazepam 2 mg Tablets / tablets immediate release in order to establish that there are no significant pharmacokinetic differences.

Detailed Description

To establish the main pharmacokinetic variables of the two formulations.

Conditions

Healthy; Healthy Donors

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Period 1

Rivotril® 2 mg

Group Type: ACTIVE_COMPARATOR

Rivotril®

Intervention Type: DRUG

Rivotril® 2 mg

Period 2

Clonazepam TQ 2 mg

Group Type: ACTIVE_COMPARATOR

Clonazepam TQ 2 mg

Intervention Type: DRUG

Test

Interventions

Rivotril®

Rivotril® 2 mg

Intervention Type: DRUG

Clonazepam TQ 2 mg

Test

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Women and men between 18 and 50 years of age at the time of signing the informed consent form.
• Women who are not capable of conceiving (To be considered not capable of conceiving she must be at least 1 year postmenopausal or surgically sterile) or who are not pregnant or breastfeeding.
• Women of childbearing capacity must be using adequate contraception for the past 6 months and agree to continue using adequate contraception for 30 days after signing the consent form.
• Have been clinically diagnosed as healthy by the study physician.
• Subjects with the clinical laboratory results requested in the protocol (Table 2) within normal ranges and/or fit by medical selection. Current for 3 months.
• Subjects non-smokers for the last 3 months at the time of signing the informed consent.
• Having signed the informed consent for the study.
• Subjects sexually active or of reproductive age must use an effective contraceptive method during and for at least 7 days after the end of the study.
• Body mass index between 18-30 kg/m2 at the time of inclusion in the study.
• Subject with complete contact information (cell phone and/or landline contact, address).
• Subject with a family member or guardian with a contact telephone number.
• Subject with the availability of time to comply with the scheduled visits and activities.
• Subject willing to comply with the prohibitions and restrictions specified in this protocol.

Exclusion Criteria

• Subject with a diagnosis of renal, cardiac, hepatic, immunological, dermatological, endocrine, gastrointestinal, neurological or psychiatric disease, compulsive depressive disorder.
• Subject with diagnosis of hematological disorders, such as anemias and/or polycythemia.
• Subjects with history of gastric surgeries.
• Permanent or temporary use during the last 5 days prior to the administration of the investigational product of the study of any type of medication either on their own initiative or by medical prescription. Except female patients who are planning regularly with the same contraceptive method in the last 6 months prior to the start of the present study.
• Pregnant or breastfeeding women (Table 2).
• Xanthine consumption from coffee, tea or chocolate during the 48 hours prior to hospitalization.
• Alcohol consumption of more than 16 g per week equivalent to 1 beer or 2 glasses of wine during the 5 days prior to administration of the investigational product.
• Positive test for consumption of drugs of abuse or psychoactive substances at the time of screening or prior to administration of the investigational product. (Table 2)
• Known hypersensitivity to the active substance or excipients of the test product.
• Medical history of angioedema or anaphylaxis.
• Subject diagnosed with human immunodeficiency virus, hepatitis B (surface antigen) or hepatitis C (surface antigen) positive infection.
• Having participated in clinical trials in the 4 months prior to the time of signing the informed consent.
• Have donated blood or reported blood loss greater than 500 mL in the 30 days prior to the time of investigational product administration.
• Subject with clinically significant acute illness or temperature > 38°C within 24 hours prior to administration of the investigational product.
• Subject with any contraindication to blood collection due to bleeding disorders or thrombocytopenia.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Centro de Atencion e Investigacion Medica

NETWORK

Sponsor Role: lead

Responsible Party

Humberto Reynales MD MSc PhD

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Central Contacts

Mauricio - Vargas, Ms

Role: CONTACT

mauricio.vargas@caimed.com

+57 3138590569

Constanza N Morales, MD

Role: CONTACT

comite.epidemiologia@caimed.com

57(601) 8707070

Other Identifiers

CLONAZ-BIO-002-2023

Identifier Type: -

Identifier Source: org_study_id