Pharmacokinetics and Bioequivalence of Doxylamine+Pyridoxine and Diclectin Under Fed Conditions in Healthy Volunteers

NCT ID: NCT06342778

Last Updated: 2025-07-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-02-27
• Study Completion Date: 2024-05-02

Brief Summary

This study aims to evaluate pharmacokinetic profile and establish bioequivalence of the investigational drug Doxylamine + Pyridoxine, enteric-soluble, film-coated tablets, 10 mg + 10 mg (Valenta Pharm JSC, Russia) compared to the reference drug Diclectin, delayed-release tablets, 10 mg + 10 mg (registration certificate holder - Tzamal Bio-Pharma, Israel, manufacturer - Duchesnay Inc, Canada) in healthy volunteers under fed conditions.

Conditions

Nausea

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

RT-sequence

Group 1 (14 volunteers, RT sequence) will take 2 tablets of Diclectin in Period 1 and 2 tablets of Doxylamine + Pyridoxine in Period 2

Group Type: EXPERIMENTAL

Doxylamine + Pyridoxine

Intervention Type: DRUG

A single dose of R or T drug in each of 2 periods of the study under fed conditions

Diclectin

Intervention Type: DRUG

A single dose of R or T drug in each of 2 periods of the study under fed conditions

TR-sequence

Group 2 (14 volunteers, TR sequence) will take 2 tablets of Doxylamine + Pyridoxine in Period 1 and 2 tablets of Diclectin in Period 2

Group Type: ACTIVE_COMPARATOR

Doxylamine + Pyridoxine

Intervention Type: DRUG

A single dose of R or T drug in each of 2 periods of the study under fed conditions

Diclectin

Intervention Type: DRUG

A single dose of R or T drug in each of 2 periods of the study under fed conditions

Interventions

Doxylamine + Pyridoxine

A single dose of R or T drug in each of 2 periods of the study under fed conditions

Intervention Type: DRUG

Diclectin

A single dose of R or T drug in each of 2 periods of the study under fed conditions

Intervention Type: DRUG

Other Intervention Names

Doxylamine + Pyridoxine, enteric soluble film-coated tablets; Doxylamine + Pyridoxine, Delayed-release Tablets

Eligibility Criteria

Inclusion Criteria

1. Voluntary and personally signed informed consent form by the heathy subject prior to initiation of any study procedures.

2. Women of childbearing potential (18 to 49 years inclusive).

3. Verified "healthy" status with no abnormalities detected based on clinical, laboratory, and instrumental examinations specified in the study protocol.

4. Blood pressure (BP) level: systolic blood pressure (SBP) from 100 to 139 mmHg, diastolic blood pressure (DBP) from 60 to 89 mmHg (inclusive).

5. Heart rate (HR) from 60 to 90 beats per min (inclusive).

6. Respiratory rate (RR) 12 to 18 breaths per min (inclusive).

7. Body temperature from 36 to 36.9°C (inclusive).

8. Body mass index (BMI) of 18.5 ≤ BMI ≤ 30 kg/m², with body weight ≥ 45 kg.

9. Consent to use adequate contraceptive methods throughout the study and for 30 days after completion of the study, negative pregnancy test.

10. Volunteers must demonstrate appropriate behavior and coherent speech.

1. Positive allergic history.

2. History of hypersensitivity to the active ingridient and/or excipients of the study drugs.

3. A history of drug intolerance to the active ingridient and/or excipients of the study medications.

4. Chronic diseases of cardiovascular, lymphatic, respiratory, nervous, endocrine, digestive, musculoskeletal, integumentary, immune systems, as well as genitourinary apparatus and hematopoietic organs.

5. Clinically significant deviations from normal reference values for laboratory and diadnostic parameters based on local laboratory standarts.

6. History of gastrointestinal tract surgery (excluding appendectomy performed at least 1 year prior to screening).

7. Diseases/conditions that, in the investigator's judgement, may affect the absorption, distribution, metabolism, or excretion of study drugs.

8. Acute infectious diseases within 4 weeks prior to screening.

9. Use of medications with significant effects on hemodynamics or those affecting liver fuction (barbiturates, benzodiazepines, omeprazole, cimetidine, etc.) within 1 month prior to screening.

10. Regular use of medicatins within 3 weeks prir to screening or single-dose medication intake within 7 days prior to screening.

11. Blood or plasma donation within 3 months prior to the Screening Visit.

12. Use of hormonal contraceptives within 2 months prior to the Screening Visit.

13. Use of depot injections of any medications within 3 months prior to the Screening Visit.

14. Pregnancy or lactation period, positive pregnancy test.

15. Participation in another clinical trial less than 3 months prior to screening or concurrently with the present study.

16. Consumption of more than 10 units of alcohol (1 unit of alcohol is equivalent to 500 mL of beer, 200 mL of wine, or 50 mL of spirits) per week in the last month prior to inclusion in the study or history of alcoholism, drug abuse, or medicines abuse.

17. Smoking.

18. Positive blood test for antibodies to human immunodeficiency virus (HIV) types 1 and 2, antibodies to Treponema pallidum antigens, hepatitis B surface antigen (HBsAg), antibodies to hepatitis C virus antigens, rapid test (nasopharyngeal and/or oropharyngeal swab) for SARS-Cov-2 (COVID-19).

19. Clinically significant abnormalities on electrocardiogram (ECG).

20. Positive urinalysis for narcotics and potent drugs.

21. Positive breath alcohol vapor test.

22. Scheduling a hospital stay during the study period, for any reason other than hospitalization required by this protocol.

23. Inability or inability to comply with the requirements of the protocol, to follow the procedures prescribed by the protocol, to follow the diet, activity regime.

24. Observance of religious fasting or special diet (e.g., vegetarian, vegan).

25. Other conditions that, in the Investigator's judgement, may interfere with the volunteer's participation in the study or lead to early withdrawal, including lifestyle factors such as night shift work or extreme physical exertion.

5. Volunteer developing a severe and/or serious adverse event during the study.

6. Missing collection of 2 or more consecutive blood samples, or 3 or more blood samples within a single period of pharmacokinetic part of the study.

7. Occurrence of vomiting/diarrhea within 24 h after administration of the study drug (the choice of time interval is based on the value of tmax parameter for doxylamine and pyridoxal-5-phosphate, not exceeding 7.2 ± 1.9 and 11.7 ± 5.3 h, respectively, according to the manufacturer of the reference drug).

8. Positive urine test for narcotics and potent drugs.

9. Positive breath alcohol vapor test.

10. A positive pregnancy test.

11. A positive test for SARS-Cov-2 (COVID-19);

12. Development of any new condition or situation that hinders protocol-defined procedures.

Exclusion Criteria

1. Refusal by the volunteer to continue participation in the study.

2. Failure of the volunteer to comply with study protocol requirements, including missed visits, unauthorized use of prohibited medications, or non-adherence to dietary and lifestyle restrictions.

3. Occurrence of safety-related issues during the study that endanger the subject (e.g. hypersensitivity reactions, etc.).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 49 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Valenta Pharm JSC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

State budgetary health care institution Yaroslavl region "Clinical Hospital № 3"

Yaroslavl, , Russia

Countries

Russia

Other Identifiers

DIP-05-02-2023

Identifier Type: -

Identifier Source: org_study_id