Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12616000418471
Ethics application status
Approved
Date submitted
30/03/2016
Date registered
1/04/2016
Date last updated
20/12/2018
Date data sharing statement initially provided
20/12/2018
Date results provided
20/12/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Pharmacokinetic study of four orally formulated combinations of acetaminophen and ibuprofen in healthy volunteers under fasting conditions
Scientific title
A single dose, four-way, open-label study to determine the pharmacokinetics and bioavailability of an oral suspension of combined acetaminophen and ibuprofen, a powder sachet of combined acetaminophen and ibuprofen for oral solution and two tablet formulations of combined acetaminophen and ibuprofen in 28 healthy volunteers under fasting conditions.
Secondary ID [1] 288873 0
AFT-MX-14A
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Pain relief 298167 0
Condition category
Condition code
Anaesthesiology 298332 298332 0 0
Pain management

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Each participant will be randomly allocated to receive a single dose of each of the following treatments in a four-way cross-over sequence:
- Treatment A: oral suspension containing 1000 mg acetaminophen + 300 mg ibuprofen in 31.25 mL
- Treatment B: powder sachet containing 1000 mg acetaminophen + 300 mg ibuprofen for oral solution
- Treatment C: tablets providing total dose of 1000 mg acetaminophen + 300 mg ibuprofen
- Treatment D: tablets providing total dose of 975 mg acetaminophen + 292.5 mg ibuprofen

The administration of doses will be supervised on site.
All treatments will be administered under fasting conditions. Participants will be fasted for at least 10 hours overnight before dosing and for 3 hours after dosing. Water will be restricted for 1 hour pre-dose and 1 hour post-dose (with the exception of water administered as part of dosing).

Administration
- Oral Suspension formulation: 31.25 mL of the oral suspension will be dispensed for consumption. Any residue remaining after initial administration will be resuspended with 240 mL of water and consumed.
- Powder Sachet formulation: contents of the sachet will be dissolved in 240 mL hot water and consumed once cold.
- Tablet Formulations: will be administered with 240 mL of water.

Dose-frequency is single doses of four different formulations separated by a washout period of 3 days.
All participants will complete the four periods in cross-over fashion.

Intervention code [1] 294333 0
Treatment: Drugs
Comparator / control treatment
Treatment C: tablets providing total dose of 1000 mg acetaminophen + 300 mg ibuprofen
Control group
Active

Outcomes
Primary outcome [1] 297804 0
To determine the pharmacokinetic parameters (Cmax, AUC(0-t), AUC(0-inf), Tmax, Kel, t1/2) of acetaminophen and ibuprofen and compare between four treatment groups, under fasting conditions.
Timepoint [1] 297804 0
Single-dose study measuring plasma concentration of acetaminophen and ibuprofen pre-dose and at 5, 15, 30, 45 minutes and 1.00, 1.25, 1.50, 2.00, 3.00, 6.00, 8.00, 10.00 and 12.00 hours after study drug administration.
Secondary outcome [1] 322289 0
An acute safety evaluation will be performed during each study period by recording spontaneously reported adverse events and by clinical assessments.
Known NSAID adverse effects (i.e. GI ulceration, indigestion/stomach pain, GI bleeding, bronchospasm, water retention, renal failure, skin reactions and thromboembolic events), and known adverse effects of acetaminophen (i.e. clinical evidence of hepatotoxicity) will be compared between groups.
Adverse events will continue to be assessed up to 7 days after the last dose of the study medication by spontaneous reporting and at a final follow-up phone call.
Timepoint [1] 322289 0
Safety will be evaluated during each study period (from administration to 12 hours post administration for each formulation), and for 7 days following study drug administration.

Eligibility
Key inclusion criteria
Healthy subjects, males and females aged 18 to 50 years of age.
Females must be sterile or using adequate contraception.
Participants must not have taken any prescription medications for at least 14 days or over-the-counter medications for at least 3 days before the start of each study phase, with the exception of oral contraceptives and the study medication.
All subjects must be deemed healthy on the basis of a medical history, physical exam (including vital signs and 12-lead ECG recording), urinalysis, and blood biochemical, haematological and serological examinations.
Minimum age
18 Years
Maximum age
50 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Women who are pregnant, nursing, unwilling to take adequate contraceptive precautions or undergo a urine pregnancy test
Excess weekly alcohol consumption
History of drug abuse
Smoking > 10 cigarettes per day
Unwilling to abstain from smoking throughout duration of the study
Unable to abstain from prescription drugs within 14 days prior to the study, vitamins within 2 days prior to the study, grapefruit containing foods or beverages within 7 days prior to the study or caffeine containing foods or beverages within 24 hours prior to the study
Used OTC herbal products within 3 days prior to the study
Participating in another clinical trial within 80 days
Clinically significant abnormal laboratory tests.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Crossover
Other design features
Phase
Phase 1
Type of endpoint/s
Pharmacokinetics
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/05/2016
Actual
14/07/2016
Date of last participant enrolment
Anticipated
Actual
24/07/2016
Date of last data collection
Anticipated
Actual
4/08/2016
Sample size
Target
28
Accrual to date
Final
28
Recruitment outside Australia
Country [1] 7754 0
Jordan
State/province [1] 7754 0
Amman

Funding & Sponsors
Funding source category [1] 293225 0
Commercial sector/Industry
Name [1] 293225 0
AFT Pharmaceuticals Ltd
Country [1] 293225 0
New Zealand
Primary sponsor type
Commercial sector/Industry
Name
AFT Pharmaceuticals Ltd
Address
Level 1, 129 Hurstmere Rd
Takapuna
Auckland, 0622
New Zealand
Country
New Zealand
Secondary sponsor category [1] 292027 0
None
Name [1] 292027 0
Address [1] 292027 0
Country [1] 292027 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 294705 0
International Pharmaceutical Research Centre (IPRC)
Ethics committee address [1] 294705 0
Ethics committee country [1] 294705 0
Jordan
Date submitted for ethics approval [1] 294705 0
01/04/2016
Approval date [1] 294705 0
05/04/2016
Ethics approval number [1] 294705 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 64686 0
Dr Majdi Abu Awida
Address 64686 0
International Pharmaceutical Research Centre (IPRC)
1 Queen Rania Street
Sport City Circle
Amman 11196
Jordan
Country 64686 0
Jordan
Phone 64686 0
+962-6-5627648
Fax 64686 0
Email 64686 0
[email protected]
Contact person for public queries
Name 64687 0
Hartley Atkinson
Address 64687 0
AFT Pharmaceuticals Ltd
Level 1, 129 Hurstmere Rd
Takapuna
Auckland, 0622
New Zealand
Country 64687 0
New Zealand
Phone 64687 0
+6494880232
Fax 64687 0
Email 64687 0
[email protected]
Contact person for scientific queries
Name 64688 0
Hartley Atkinson
Address 64688 0
AFT Pharmaceuticals Ltd
Level 1, 129 Hurstmere Rd
Takapuna
Auckland, 0622
New Zealand
Country 64688 0
New Zealand
Phone 64688 0
+6494880232
Fax 64688 0
Email 64688 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.