check_circleStudy Completed
Bioequivalence, Healthy volunteers, Platelet aggregation inhibition
Bayer Identifier:
22518
ClinicalTrials.gov Identifier:
EudraCT Number:
Not Available
EU CT Number:
Not Available
A Study to Learn if There is a Difference in the Blood Levels of Acetylsalicylic Acid When Taken as Different Chewable Tablets on an Empty Stomach by Healthy Participants
Trial purpose
In this study, researchers want to learn if 2 different forms of acetylsalicylic acid (ASA) chewable tablets will have the same effect in the body. For this, they compared the blood levels of a new form of ASA chewable tablet, which is manufactured at a different site, with an approved ASA chewable tablet, on an empty stomach in healthy participants. This is done as part of the regulatory requirement for the marketing approval of the new ASA chewable tablet.
The study treatment, ASA, is an antiplatelet drug. It works by making the blood thinner and stopping the blood from clotting.
In this study, participants will be healthy and will not benefit from taking ASA chewable tablets. However, the study will provide information on how the new ASA chewable tablet, which is manufactured at a different site, has an effect on the body.
The main purpose of this study is to compare blood levels of the new ASA chewable tablet with the approved ASA chewable tablet when taken as a single dose on an empty stomach.
For this, the researchers will analyze:
- Area under the curve (AUC): a measure of the total amount of ASA in participants’ blood over time
- Maximum observed concentration (Cmax): the highest amount of ASA in participants’ blood after a single dose without food
This study will have 3 treatment periods of 4 days each. In each period, participants will take either the new or approved ASA chewable tablet on an empty stomach according to the order assigned to them. The 2 treatment sequences in this study are:
New chewable tablet, approved chewable tablet, new chewable tablet
Approved chewable tablet, new chewable tablet, approved chewable tablet
Each participant will be in the study for around 7 weeks, which includes:
- a visit within 21 days of the first period to confirm if the participant can take part in the study
- hospital stay of around 2 days in each period, during which, participants will take their assigned treatment, and have blood tests to check for drug levels
- a gap of 1 week after taking the treatment in each period
During the study, the doctors and their study team will:
- measure the level of the study treatment by taking blood samples
- check participants’ health by performing urine tests, checking vital signs and checking heart health using an electrocardiogram (ECG)
- ask the participants questions about how they are feeling and what adverse events they are having
An adverse event is any medical problem that a participant has during a study. The study doctors keep track of all adverse events, irrespective if they think it is related or not to the study treatment.
As this study is conducted in healthy participants who will not benefit from the treatment, access to the treatment after the study is not planned.
The study treatment, ASA, is an antiplatelet drug. It works by making the blood thinner and stopping the blood from clotting.
In this study, participants will be healthy and will not benefit from taking ASA chewable tablets. However, the study will provide information on how the new ASA chewable tablet, which is manufactured at a different site, has an effect on the body.
The main purpose of this study is to compare blood levels of the new ASA chewable tablet with the approved ASA chewable tablet when taken as a single dose on an empty stomach.
For this, the researchers will analyze:
- Area under the curve (AUC): a measure of the total amount of ASA in participants’ blood over time
- Maximum observed concentration (Cmax): the highest amount of ASA in participants’ blood after a single dose without food
This study will have 3 treatment periods of 4 days each. In each period, participants will take either the new or approved ASA chewable tablet on an empty stomach according to the order assigned to them. The 2 treatment sequences in this study are:
New chewable tablet, approved chewable tablet, new chewable tablet
Approved chewable tablet, new chewable tablet, approved chewable tablet
Each participant will be in the study for around 7 weeks, which includes:
- a visit within 21 days of the first period to confirm if the participant can take part in the study
- hospital stay of around 2 days in each period, during which, participants will take their assigned treatment, and have blood tests to check for drug levels
- a gap of 1 week after taking the treatment in each period
During the study, the doctors and their study team will:
- measure the level of the study treatment by taking blood samples
- check participants’ health by performing urine tests, checking vital signs and checking heart health using an electrocardiogram (ECG)
- ask the participants questions about how they are feeling and what adverse events they are having
An adverse event is any medical problem that a participant has during a study. The study doctors keep track of all adverse events, irrespective if they think it is related or not to the study treatment.
As this study is conducted in healthy participants who will not benefit from the treatment, access to the treatment after the study is not planned.
Key Participants Requirements
Sex
AllAge
18 - 55 YearsTrial summary
Enrollment Goal
38Trial Dates
February 2025 - April 2025Phase
Phase 1Could I Receive a placebo
NoProducts
Aspirin (Acetylsalicylic acid, BAYE004465)Accepts Healthy Volunteer
YesWhere to participate
Status | Institution | Location |
---|---|---|
Not yet recruiting | IPharma, S.A. de C.V. | Monterrey, 64460, Mexico |
Primary Outcome
- AUC(0-tlast) of ASAAUC(0-tlast): AUC from time 0 to the last data point > lower limit of quantitation (LLOQ)date_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
- Cmax of ASAdate_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
Secondary Outcome
- AUC of ASA and salicylic aciddate_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
- Ke of ASA and salicylic aciddate_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
- t1/2 of ASA and salicylic acidt1/2: half-life associated with the terminal slopedate_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
- tmax of ASA and salicylic acidtmax: time to reach Cmax (in case of two identical Cmax values, the first tmax will be used)date_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
- Cmax of salicylic aciddate_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
- AUC(0-tlast) of salicylic aciddate_rangeTime Frame:Baseline (pre-dose) and at 0.083, 0.166, 0.250, 0.333, 0.416, 0.500, 0.583, 0.666, 0.750, 0.833, 0.916, 1.00, 1.25, 1.50, 2.00, 3.00, 4.00, 4.50, 5.00, 7.00, 9.00, 12.00 and 24.00 hours post dose in each treatment period
Trial design
Trial Type
InterventionalIntervention Type
DrugTrial Purpose
OtherAllocation
RandomizedBlinding
N/AAssignment
Crossover AssignmentTrial Arms
2