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Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg/5ml and Nurofen®, Oral Suspension 100 mg/5 ml in Healthy Volunteers Under Fasting Conditions

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ClinicalTrials.gov Identifier: NCT03561558
Recruitment Status : Completed
First Posted : June 19, 2018
Last Update Posted : November 1, 2018
Sponsor:
Collaborator:
ClinPharmInvest, LLC
Information provided by (Responsible Party):
Pharmtechnology LLC

Brief Summary:
To demonstrate bioequivalence of single dose test formulation of Ibuprofen,oral suspension 200 mg/5 ml (containing ibuprofen 200 mg) of Pharmtechnology LLC, Republic of Belarus with reference Nurofen® for Children, oral suspension 100 mg / 5 ml (containing ibuprofen 100 mg) of "Reckitt Benckiser Healthcare International Ltd, .", UK in normal, healthy, adult, human subjects under fasting conditions.To monitor adverse events and ensure the safety

Condition or disease Intervention/treatment Phase
Healthy Drug: Ibuprofen D Drug: Nurofen® for Children Phase 1

Detailed Description:
Total 30 normal healthy adult subjects will be enrolled in the study. Subjects will be administered either the Test (5 ml of oral suspension containing 200 mg of ibuprofen) or the Reference Product (10ml of oral suspension containing 200 mg of ibuprofen) with 200 mL of water in each period as per the randomization schedule. Subjects will fast for at least 10 hours prior to administration of the study drugs and for four (4) hours after administration of the study drugs during each study period. Standardized meals will be provided in each study period. Water will not be accessible to the subjects 1 hour to administration of the study drugs and 2 hours after administration of the study drugs in each period. A total of 20 blood samples will be withdrawn for pharmacokinetic profiling during each study period. The plasma concentrations of R- and S-enantiomers of ibuprofen will be measured by a validated LC-MS/MS analytical method. ANOVA will be performed on log transformed pharmacokinetic parameters Cmax, AUC0-t and 90% confidence interval will be constructed for the ratio of geometric least square mean of the Test and Reference products, obtained from the log-transformed data. Bioequivalence will be concluded if the ratio estimate as well as its 90% confidence interval of S-enantiomers of ibuprofen, both falls within the acceptable range of 80.00% to 125.00% for Cmax, AUC0-t.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 30 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Masking Description: This study is an open label study; the subjects and the investigator will not be blinded towards the identity of the investigational products. However, analysts will be blinded towards identity of investigational products administered.
Primary Purpose: Other
Official Title: Open, Randomized, Cross-over, Two Period, Two-sequence, One-center, Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg / 5ml (Pharmtechnology, Belarus) and Nurofen® for Children, Oral Suspension 100 mg / 5 ml (Reckitt Benckiser Healthcare International Ltd, UK) in Healthy Volunteers Under Fasting Conditions
Actual Study Start Date : June 11, 2018
Actual Primary Completion Date : June 24, 2018
Actual Study Completion Date : June 25, 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Ibuprofen D, oral suspension
Ibuprofen oral suspension, 200 mg/ 5 ml is the test product. In period 1 and period 2, 15 of 30 subjects will be given single oral dose (5 ml containing 200 mg of ibuprofen) of suspension.
Drug: Ibuprofen D
Ibuprofen D, oral suspension, 200 mg / 5ml, manufactured by LLC Pharmtechnology, Belarus

Active Comparator: Nurofen® for Children, oral suspension
Nurofen® for Children oral suspension, 100 mg/ 5 ml is the reference product. In period 1 and period 2, 15 of 30 subjects will be given single oral dose (10 ml containing 200 mg of ibuprofen) of suspension.
Drug: Nurofen® for Children
Nurofen® for Children, Oral Suspension, 100 mg / 5 ml, marketed by Reckitt Benckiser Healthcare International Ltd, UK




Primary Outcome Measures :
  1. Primary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Peak Plasma Concentration (Cmax)

  2. Primary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Area under the plasma concentration versus time curve from time 0 to the last measured concentration (AUC0-t)


Secondary Outcome Measures :
  1. Safety and tolerability of the investigational products (testing and reference) [ Time Frame: 22 days ]
    Number of adverse events, number of deaths, number of severe adverse events in subjects who have taken at least one dose of investigational products.

  2. Secondary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Area under the plasma concentration versus time curve from time 0 to to infinite time(AUC0-∞)

  3. Secondary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Time of maximum measured plasma concentration (Tmax)

  4. Secondary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Elimination or terminal half-life (T1/2)

  5. Secondary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Elimination rate constant (Kel)

  6. Secondary pharmacokinetic parameter for S-enantiomer of ibuprofen [ Time Frame: 8 days ]
    Residual area (AUCresid)



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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Healthy adult human subjects, aged between 18 to 45 years.
  2. Subjects with Body Mass Index (BMI) 18.5 to 30 kg/m2.
  3. Female subjects with a negative pregnancy test.
  4. Non-lactating females.
  5. If subject is a female and is of child bearing potential, she should be practicing an acceptable non-hormonal method of birth control for the duration of the study(at least 14 days before the start of the study, throughout the study and 14 days after the completion of the study), such as a combination of male condom and diaphragm with spermicide.
  6. If subject is a male and and has a female partner of child bearing potential, he should be practicing an acceptable method of birth control for the duration of the study(at least 14 days before the start of the study, throughout the study and 14 days after the completion of the study), such as a combination of male condom and spermicide (double barrier method).
  7. Subjects having no clinically significant medical history and no clinically significant abnormalities in general physical examination, laboratory assessments, 12-lead ECG, chest X-Ray or vital signs.
  8. Subjects are able to understand the requirements of the study, to sign a written informed consent, and also to accept all the restrictions imposed during the course of the study, and to agree to return for the required investigations.

Exclusion Criteria:

  1. Subjects with a known history of allergic disorders.
  2. Subjects with a known history of drug hypersensitivity to ibuprofen d or any excipients of the formulation.
  3. Subjects with a known history of drug intolerance.
  4. Subjects with history of psychiatric disorders.
  5. Subjects with history of epilepsy, seizures, other neurological disorders.
  6. Subjects on a low sodium diet for 2 weeks before the start study, or on any special diet (for example, vegetarian, vegan) or follow a special lifestyle (night shifts,extreme physical work).
  7. Use of hormonal contraceptives either oral or implants within 6 months prior to first period dosing.
  8. Female subjects of child bearing potential who have had an unprotected sexual intercourse with an unsterilized male sexual partner within 30 days before the start of the study
  9. Use of any xanthine-containing food or beverages (tea, coffee, chocolates, soft drinks like cola, etc.) for at least 72 hours prior to the start of the study.
  10. Use of citrus fruits (including grapefruit and grapefruit juice) and cranberries (including juices,etc.) for at least 14 days prior to the start of the study.
  11. Subjects with a history of disorders of cardiovascular, bronchopulmonary, neuroendocrine system, and also the gastrointestinal tract, liver, kidney and blood.
  12. Subjects with a history of other disorders that, at the discretion of the Principal Investigator, can affect absorption, distribution, metabolism or excretion of both drugs or increase the risk of adverse effects.
  13. Subjects with a history of surgical interventions on the gastrointestinal tract except for appendectomy.
  14. Subjects with a history acute infectious illnesses within 4 weeks prior to the start of the study.
  15. Subjects with abnormalities in resting heart rate (>80 beats/min or <60 beats/min), blood pressure either hypotensive episode (systolic blood pressure <100 mmHg or diastolic blood pressure <70 mmHg) or hypertension (systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥90 mmHg), in ECG
  16. Use of known inhibitors or inducers of liver function, in particular isoenzyme CYP 3A4 (example of inducers: omeprazole, cimetidine, drugs, containing St. John's wort extract, barbiturates, carbamazepine, phenytoin, glucocorticoids; example of inhibitors: antiviral drugs, clarithromycin, ciprofloxacin, gestodene, etc.) within 2 months prior to the start of the study.
  17. Use of any drugs with systemic absorption within14 days prior to the start of the study.
  18. Use of OTC drugs, including herbs and nutritional supplements within 7 days prior to the Dosing Date. (including vitamins and natural food additives, phyto supplements,herbal preparations such as, cat's claw, angelica officinalis, oenothera, feverfew, garlic, ginger, ginkgo, red clover, horse chestnut, green tea, ginseng).
  19. Depot injection or implants of any drugs within 3 months prior to the start of the study.
  20. Donation of plasma or blood (450 ml or more) within 2 months prior to the start of the study.
  21. Intake of more than 10 units alcohol per week (1 unit of alcohol is equivalent to ½ liter of beer, 200 ml dry wine or 50 ml of spirits) or history alcoholism, drug addiction, drug abuse.
  22. Smoking more than 10 cigarettes per day.
  23. Participation in other clinical trials of medicines within 3 months prior to the start of the study.
  24. Positive test for syphilis, hepatitis B, hepatitis C or HIV.
  25. Positive pregnancy test (for female subjects with child bearing potential).
  26. Breast-feeding.
  27. Positive test for alcohol.
  28. Positive urinary screen test for drugs of abuse.
  29. Subjects with a history of a rare hereditary intolerance to galactose and/or sucrose, a deficiency of lactase, glucose-galactose malabsorption syndrome.
  30. Subjects with clinically significant abnormal laboratory values and results of imaging studies.
  31. Subjects who refuse to comply with the study protocol and/or not credible therein and who are, at the discretion of the Principal Investigator, unable to understand and assess the information about the study, expected risks and possible discomfort in the process of signing written informed consent.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03561558


Locations
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Russian Federation
State Autonomous Healthcare Facility of the Yaroslavl Region "Clinical Hospital No. 2"
Yaroslavl, Yaroslavl Region, Russian Federation, 150010
Sponsors and Collaborators
Pharmtechnology LLC
ClinPharmInvest, LLC
Investigators
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Principal Investigator: Alexander Khokhlov, Professor ClinPharmInvest, LLC

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Responsible Party: Pharmtechnology LLC
ClinicalTrials.gov Identifier: NCT03561558     History of Changes
Other Study ID Numbers: FRM-03-IBU/21/11/17
First Posted: June 19, 2018    Key Record Dates
Last Update Posted: November 1, 2018
Last Verified: June 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Plan Description: The Company may provide the individual participant data after privacy protection on case by case basis.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Pharmtechnology LLC:
Bioequivalence
Additional relevant MeSH terms:
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Ibuprofen
Anti-Inflammatory Agents, Non-Steroidal
Analgesics, Non-Narcotic
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Inflammatory Agents
Antirheumatic Agents
Cyclooxygenase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action