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Trial registered on ANZCTR


Registration number
ACTRN12613001134718
Ethics application status
Approved
Date submitted
9/10/2013
Date registered
11/10/2013
Date last updated
13/10/2014
Type of registration
Prospectively registered

Titles & IDs
Public title
Comparative assessment of the absorption of a generic formulation of quetiapine prolonged release tablet against the innovator quetiapine tablet conducted under fasting conditions and at steady state in healthy male and female volunteers
Scientific title
A multiple dose, randomized, blinded, bioequivalence study of quetiapine prolonged release tablets in a 2 way crossover comparison against the innovator quetiapine tablet conducted under fasting conditions and at steady state in healthy male and female volunteers
Secondary ID [1] 283382 0
None
Universal Trial Number (UTN)
U1111-1148-4683
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Bioequivalence study conducted in healthy volunteers comparing two formulations of quetiapine with no health condition or problem studied.

Although this study is being conducted in healthy volunteers who are not being treated for the condition to which the medicine is used, quetiapine belongs to a class of medicines called an atypical antipsychotic drug and is prescribed for the maintenance treatment of Bipolar and schizophrenia.
290280 0
Condition category
Condition code
Other 290667 290667 0 0
Research that is not of generic health relevance and not applicable to specific health categories listed above

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Multiple dose, crossover over study design whereby each participant receives the test formulation of quetiapine (1 x 200 mg) on five occasions and the innovator formulation of desvenlafaxine (1 x 200 mg) on five occasions with each dose seperated by a 10 day washout period.

On study days 1-5 subjects will receive 5 daily doses of one formulation (either the test or innovator) and on study days 15-19 they will receive 5 daily doses of the other formulation (either the innovator or test).

Each dose (1 x 200 mg) will be taken orally with 240 ml of water at ambient temperature. Medication must be swallowed whole and a mouth check will be conducted to ensure the medication has been taken as directed.

Participants are required not to eat for 10 hours before receiving each dose.

On study days 1 to 4 and 15 to 18 subjects will report to Zenith Technology for dosing and the provision of one blood sample. They will then be given a light breakfast to consume following each dose at home.

On study day 5 and 19 no water is allowed for 1 hour prior to dosing until 1 hour after dosing (except for the water consumed with the dose) and are required to fast for approximately 4 hours after receiving each dose. Bathroom visits will be supervised to ensure no unauthorised water or food intake and for personal safety. Participants will be confined at the Clinical Site for 10 hours prior to dosing to ensure compliance can be monitored and for 24 hours after dosing.
Intervention code [1] 288105 0
Treatment: Drugs
Comparator / control treatment
Mulitple dose, crossover over study design whereby each participant receives the test formulation of quetiapine (1 x 200 mg prolonged release) on five occasions and the innovator formulation of quetipine (1 x 200 mg prolonged release) on five occasion with each dose seperated by a 10 day washout period. The comparator/control for this trial is the innovator formulation of quetiapine.
Control group
Active

Outcomes
Primary outcome [1] 290686 0
To compare the bioavailability of quetiapine (as summarised by AUC0-t(ss), Cmax(ss) and Cmin(ss)) for the two formulations. All plasma samples will be assayed for quetiapine using a fully validated LC/MS/MS method. Validation will be conducted to comply with EU and FDA guidelines.

Timepoint [1] 290686 0
Pre-dose samples on study days 1 to 4 and 15 and 18 and 0, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 9.0, 10.0, 12.0, 16.0, 20.0 and 24.0 hours on study days 5 and 19
Secondary outcome [1] 305038 0
Time to maximum peak concentration (Tmax) and the elimination half life (t1/2). Tmax will be the time where the maximum concentration occurred in the sample points. T1/2 = 0.693/Kel where kel is the terminal elimination rate constant.
Timepoint [1] 305038 0
Pre-dose samples on study days 1 to 4 and 15 and 18 and 0, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 9.0, 10.0, 12.0, 16.0, 20.0 and 24.0 hours on study days 5 and 19

Eligibility
Key inclusion criteria
Healthy males and non-pregnant females
Aged between 18 and 55
Non-smoker
BMI between 19 and 30
Normal, healthy individuals as determined by medical history, physical examination, ECG, blood pressure and laboratory tests
Able to provide written informed consent
Minimum age
18 Years
Maximum age
55 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Any history of recent recurrent attacks of bronchitis, asthma, migraine headaches
Concomitant drug therapy of any kind excluding prescribed hormonal contraceptives
Who have receievd an investigational compound or drug known to induce or inhibit liver enqymes within 60 days of the start of the study
Who have a history of abnormal heartbeats or frequent palpitations or who have a family history of long QTc syndrome
History or family history of depression or other mental illness, epilepsy or seizures
Sensitivity to quetiapine, any antipsychotic medicines, excipients of quetiapine
History of any conditions that might interfere with the absorption, distribution, metabolism or excretion of the drug
Who are lactose intolerant
Females who are breastfeeding or are planning to start a family within 60 days of dosing
Who are planning on having any surgical or dental procedures within 4 weeks of the study completion
Smoker (anyone who has smoked in the last 6 months)
History of alcohol or drug abuse or dependency
Participation in a drug study within 60 days of the start of the study or donated blood in the 60 days preceding the study.
Volunteers for whom the Clinical Investigator believes, for any reason, that participation would not be an acceptable risk.

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)
All formulations will be labelled as Formulation A and B. The identification of each treatment will only be known to the Managing Director and the Section Head - Trials and Regulatory Affairs.

Each participant will be identified by a 3 digit screening number and a 2 digit subject number. The screening number will be issued once the participant has given written consent to participate in the study and the two digit subject number (randomisation number) after acceptance into the study
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation list will be prepared using a computer program for a balanced two-way crossover design.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Crossover
Other design features
Phase
Phase 1
Type of endpoint/s
Bio-equivalence
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
28/10/2013
Actual
23/01/2014
Date of last participant enrolment
Anticipated
Actual
20/03/2014
Date of last data collection
Anticipated
Actual
Sample size
Target
36
Accrual to date
Final
Recruitment outside Australia
Country [1] 5492 0
New Zealand
State/province [1] 5492 0
Otago

Funding & Sponsors
Funding source category [1] 288105 0
Commercial sector/Industry
Name [1] 288105 0
Actavis Group PTC ehf
Country [1] 288105 0
Iceland
Primary sponsor type
Commercial sector/Industry
Name
Zenith Technology Corporation Limited
Address
156 Frederick Street
Dunedin 9016
Country
New Zealand
Secondary sponsor category [1] 286824 0
None
Name [1] 286824 0
Address [1] 286824 0
Country [1] 286824 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 290027 0
Southern Health & Disability Ethics Committee
Ethics committee address [1] 290027 0
Ethics committee country [1] 290027 0
New Zealand
Date submitted for ethics approval [1] 290027 0
26/09/2013
Approval date [1] 290027 0
22/10/2013
Ethics approval number [1] 290027 0
13/STH/125

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

Contacts
Principal investigator
Name 43578 0
Dr Noelyn Hung
Address 43578 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 43578 0
New Zealand
Phone 43578 0
+6434779669
Fax 43578 0
Email 43578 0
[email protected]
Contact person for public queries
Name 43579 0
Linda Folland
Address 43579 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 43579 0
New Zealand
Phone 43579 0
+6434779669
Fax 43579 0
Email 43579 0
[email protected]
Contact person for scientific queries
Name 43580 0
Cheung- Tak Hung
Address 43580 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 43580 0
New Zealand
Phone 43580 0
+6434779669
Fax 43580 0
Email 43580 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

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Documents added automatically
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