Protocol summary

Study aim
Bioequivalence study of mefenamic acid 500 mg tablets of Darou Darman Parmida pharmaceutical company compared to mefenamic acid 500 mg of Pfizer company in Turkey on healthy volunteers.
Design
The present clinical trial includes the study of the bioequivalence of mefenamic acid 500 mg tablets produced by Darou Darman Parmida pharmaceutical company in comparison with the mefenamic acid 500 mg sample of Pfizer in Turkey, after administration to 24 healthy human volunteers, two intervention administered to one group, in a cross-over manner. It is not blinded and non-randomized.
Settings and conduct
The study is carried out at Nik Azma Pars Alborz Company, located in Mahdasht Karaj. The blinded cross-over study includes two phases (oral consumption of one 500 mg mefenamic acid tablet per study and 2 times in total) with a one-week washout period on 24 fasting healthy volunteers. Then the obtained blood samples are determined.
Participants/Inclusion and exclusion criteria
Inclusion criteria: healthy volunteers; between the ages of 18 and 55; non-smokers. Exclusion criteria: volunteers with blood pressure less than 90 over 60 mm Hg or higher than 140 over 90 mm Hg.
Intervention groups
The study includes two stages as intervention 1: It includes oral consumption of mefenamic acid tablets 500 mg manufactured by Darou Darman Parmida Pharmaceutical Company in Iran and intervention 2: oral consumption of mefenamic acid tablets 500 mg manufactured by Pfizer Company in Turkey. This study will be repeated on fasting volunteers in a cross-sectional manner with an interval of one week.
Main outcome variables
Maximum plasma concentration

General information

Reason for update
Acronym
IRCT registration information
IRCT registration number: IRCT20230222057495N10
Registration date: 2023-11-11, 1402/08/20
Registration timing: prospective

Last update: 2023-11-11, 1402/08/20
Update count: 0
Registration date
2023-11-11, 1402/08/20
Registrant information
Name
Monireh Jalalipour
Name of organization / entity
Nikazma Pars Alborz company
Country
Iran (Islamic Republic of)
Phone
+98 26 3731 8748
Email address
info@naplab.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2023-11-22, 1402/09/01
Expected recruitment end date
2024-11-21, 1403/09/01
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
Bioequivalence study of mefenamic acid 500 mg tablets of Darou Darman Parmida pharmaceutical company compared to mefenamic acid 500 mg of Pfizer in Turkey on healthy volunteers.
Public title
Bioequivalence study of mefenamic acid 500 mg tablets
Purpose
Other
Inclusion/Exclusion criteria
Inclusion criteria:
Healthy volunteers aged between 18 and 55 years. Body mass index less than 30 kg per square meter. All volunteers must be non-smokers.
Exclusion criteria:
Blood pressure less than 90 on 60 mm Hg or more than 140 on 90 mm Hg. Consumption of any drugs, alcohol or tobacco products within 2 weeks before receiving the drug
Age
From 18 years old to 55 years old
Gender
Both
Phase
Bioequivalence
Groups that have been masked
No information
Sample size
Target sample size: 24
More than 1 sample in each individual
Number of samples in each individual: 0
---
Randomization (investigator's opinion)
Not randomized
Randomization description
Blinding (investigator's opinion)
Not blinded
Blinding description
Placebo
Not used
Assignment
Crossover
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Research Institute of Pharmaceutical Sciences, Tehran University of Medical Sciences
Street address
Institute of Pharmaceutical Sciences, Faculty of Pharmacy, Tehran University of Medical Sciences, Porsina Street
City
Tehran
Province
Tehran
Postal code
1417613151
Approval date
2023-10-17, 1402/07/25
Ethics committee reference number
IR.TUMS.TIPS.REC.1402.088

Health conditions studied

1

Description of health condition studied
---
ICD-10 code
ICD-10 code description

Primary outcomes

1

Description
The maximum plasma concentration of mefenamic acid
Timepoint
before starting to take the medicine and: 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10 and 12 hours after taking the medicine
Method of measurement
Liquid chromatography - spectrophotometric detector

Secondary outcomes

empty

Intervention groups

1

Description
Intervention group 1: includes the oral administration of 500 mg of mefenamic acid from Darou Darman Parmida Pharmaceutical Company of Iran on 24 fasting healthy volunteers. 5 ml of blood at time intervals before taking the drug and: 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10 and 12 hours after taking the drug, from Volunteers are taken. The cross-over study consists of two phases (oral consumption of one 500 mg mefenamic acid tablet per study and 2 times in total) with a one-week washout period (when the drug is completely removed from your blood). Mefenamic acid plasma concentration is determined by liquid chromatography-spectrophotometry method.
Category
Other

2

Description
Intervention group 2: includes the oral consumption of 500 mg of mefenamic acid from Pfizer in Turkey on 24 healthy fasting volunteers. 5 ml of blood at time intervals before taking the drug and: 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10 and 12 hours after taking the drug, from Volunteers are taken. The cross-over study consists of two phases (oral consumption of one 500 mg mefenamic acid tablet per study and 2 times in total) with a one-week washout period (when the drug is completely removed from your blood). Mefenamic acid plasma concentration is determined by liquid chromatography-spectrophotometry method.
Category
Other

Recruitment centers

1

Recruitment center
Name of recruitment center
Nik Azma Pars Alborz Laboratory
Full name of responsible person
Monireh Jalalipour
Street address
No. 419, Azadegan Square, Imam Khomeini Boulevard
City
Mahdasht Karaj
Province
Alborz
Postal code
3188913179
Phone
+98 26 3731 8748
Email
info@naplab.ir

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
Darou Darman Parmida Pharmaceutical Company
Full name of responsible person
Maryam Motaghed
Street address
No. 128, Shahid Khandi St. (Palizi), North Sohrvardi St.
City
Tehran
Province
Tehran
Postal code
1554744371
Phone
+98 21 8396
Email
info@ddp.co.ir
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
Yes
Title of funding source
Darou Darman Parmida Pharmaceutical Company
Proportion provided by this source
100
Public or private sector
Private
Domestic or foreign origin
Domestic
Category of foreign source of funding
empty
Country of origin
Type of organization providing the funding
Industry

Person responsible for general inquiries

Contact
Name of organization / entity
Nik Azma Pars Alborz laboratory
Full name of responsible person
Monireh Jalalipour
Position
Responsible Pharmacist
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
No. 419, Azadegan Square, Imam Khomeini Boulevard
City
Mahdasht Karaj
Province
Alborz
Postal code
3188913179
Phone
+98 26 3731 8748
Email
info@naplab.ir

Person responsible for scientific inquiries

Contact
Name of organization / entity
Nik Azma Pars Alborz laboratory
Full name of responsible person
Monireh Jalalipour
Position
Responsible Pharmacist
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
No. 419, Azadegan Square, Imam Khomeini Boulevard
City
Mahdasht Karaj
Province
Alborz
Postal code
3188913179
Phone
+98 26 3731 8748
Email
info@naplab.ir

Person responsible for updating data

Contact
Name of organization / entity
Nik Azma Pars Alborz laboratory
Full name of responsible person
Monireh Jalalipour
Position
Responsible Pharmacist
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
No. 419, Azadegan Squar, Imam Khomeini Boulevard
City
Mahdasht Karaj
Province
Alborz
Postal code
3188913179
Phone
+98 26 3731 8748
Email
info@naplab.ir

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Undecided - It is not yet known if there will be a plan to make this available
Study Protocol
Undecided - It is not yet known if there will be a plan to make this available
Statistical Analysis Plan
Undecided - It is not yet known if there will be a plan to make this available
Informed Consent Form
Undecided - It is not yet known if there will be a plan to make this available
Clinical Study Report
Undecided - It is not yet known if there will be a plan to make this available
Analytic Code
Undecided - It is not yet known if there will be a plan to make this available
Data Dictionary
Undecided - It is not yet known if there will be a plan to make this available
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