In- Vivo Bioequivalence study of Mesalazine 500 mg EC tablet Faran shimi Pharma with brand drugs (Asacol® 400 mg ER. Tablets. ُTillotts Pharma AG, Switzerland) in Iranian healthy volunteers.
Design
In-vivo bioequivalence study of Mesalazine 500 mg EC tablet Faran shimi Pharma in comparison with reference drug (Asacol® 400 mg ER.Tablets. ُTillotts Pharma AG, Switzerland). The single blind, Cross-over, two period, two groups (Intervention and control) and randomized (paper lottery randomization method) study with one week wash-out time.
Settings and conduct
This study is carried out in Simin Baspar Tayf-Gostar Company, Tabriz, Iran. The study population is 24 healthy Iranian volunteers.This study is a single blind study and by taking out the drugs from the existing packaging, the volunteers will not know the time of receiving the test drug and the brand. This study is a cross over study that is performed in two time periods of 72 hours with a two-week wash-out period.
Participants/Inclusion and exclusion criteria
Inclusion criteria: age between 18-60 years old; body mass index (BMI) in the range of 18-28. Exclusion criteria: history of heart, kidney and liver disease; pregnancy; drug addiction
Intervention groups
Single dose Mesalazine 500 mg EC tablet Faran shimi Pharma. Control group: Single dose Asacol® 400 mg ER. Tablets. ُTillotts Pharma AG, Switzerland
Main outcome variables
Plasma drug concentration
General information
Reason for update
Acronym
IRCT registration information
IRCT registration number:IRCT20200105046010N63
Registration date:2022-06-26, 1401/04/05
Registration timing:registered_while_recruiting
Last update:2022-06-26, 1401/04/05
Update count:0
Registration date
2022-06-26, 1401/04/05
Registrant information
Name
Javad Shokri
Name of organization / entity
Country
Iran (Islamic Republic of)
Phone
+98 41 3661 4125
Email address
shokri.j@gmail.com
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2022-06-26, 1401/04/05
Expected recruitment end date
2022-12-26, 1401/10/05
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
In- Vivo Bioequivalence study of Mesalasine 500 mg EC tablet Faran shimi Pharma with brand drugs (Asacol® 400 mg ER. Tablets. ُTillotts Pharma AG, Switzerland) in Iranian healthy volunteers.
Public title
In-vivo Bioequivalence Test of Mesalasine 500 mg EC tablet Faran shimi Pharma with brand drug (Asacol® 400 mg ER. Tablets. ُTillotts Pharma AG, Switzerland)
Purpose
Treatment
Inclusion/Exclusion criteria
Inclusion criteria:
General health
Body mass index between18-28
Informed consent
Being at the age of 18-60 years old
Exclusion criteria:
Smoking
A history of cardiovascular disease
A history of liver & kidney disease
Pregnancy
Alcohol & Drug addiction
Hypersensitivity to the drug
Age
From 18 years old to 60 years old
Gender
Both
Phase
Bioequivalence
Groups that have been masked
Care provider
Sample size
Target sample size:
24
Randomization (investigator's opinion)
Randomized
Randomization description
For this purpose, A 24- persons group will be selected and divided to two 12-persons groups randomly. The names of all volunteers will be written on paper pieces and wrapped in aluminum foils. The first 12 papers will randomly be withdrawn from bottle will be selected as group A and others will be categorized in group B.
Blinding (investigator's opinion)
Single blinded
Blinding description
Candidates are not aware of receiving the test drug or brand one. In a single study, information that could distort the test result is hidden from the candidates, but the person in charge of the test is aware of it. Test and Brand drugs are removed from their packaging by the executor and placed in similar and coded cans. Volunteers will not be informed about receiving the brand or test drug.
Placebo
Not used
Assignment
Crossover
Other design features
Secondary Ids
empty
Ethics committees
1
Ethics committee
Name of ethics committee
Ethics Committee of Tabriz University of Medical Sciences
Street address
Third floor; Central building; Tabriz University of Medical Sciences; Dneshgah St.
City
Tabriz
Province
East Azarbaijan
Postal code
5166614766
Approval date
2021-11-29, 1400/09/08
Ethics committee reference number
IR.TBZMED.REC.1400.827
Health conditions studied
1
Description of health condition studied
Bio equivalence test
ICD-10 code
ICD-10 code description
Primary outcomes
1
Description
Plasma drug concentration
Timepoint
Sampling times in this study will be 0، 1، 2، 3،4، 6، 6.5، 7، 7.5، 8، 9، 10، 10.5، 11، 12 ، 24 ,48 hours after prescribing the tablet.
Method of measurement
High Performance Liquid Chromatography with tandem mass spectroscopy detector
Secondary outcomes
empty
Intervention groups
1
Description
One test tablet ( Mesalasine 500 mg EC tablet Faran shimi Pharma ) will be received. Blood samples will be taken for 24 hours at the mentioned times after drug administration and the concentration of the drug in Plasma samples will be measured by liquid chromatography with mass spectroscopy detector
Category
Treatment - Other
2
Description
Control group: One Reference tablet Asacol® 400 mg ER. Tablets. ُTillotts Pharma AG, Switzerland will be received. Blood samples will be taken for 48 hours at the mentioned times after drug administration and the concentration of drug in plasma samples will be measured by liquid chromatography with mass spectroscopy detector.