Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12613000630718
Ethics application status
Approved
Date submitted
30/05/2013
Date registered
4/06/2013
Date last updated
10/10/2014
Type of registration
Prospectively registered

Titles & IDs
Public title
Comparative assessment of the absorption of a generic formulation of desvenlafaxine extended release tablet against the innovator desvenlafaxine extended release 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 desvenlafaxine extended release tablets in a 2 way crossover comparison against the innovator desvenlafaxine extended release tablet conducted under fasting conditions and at steady state in healthy male and female volunteers
Secondary ID [1] 282590 0
None
Universal Trial Number (UTN)
U1111-1141-1560
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Bioequivalence study conducted in healthy volunteers comparing two formulations of desvenlafaxine 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, desvenlafaxine belongs to a class of medicines called Serotonin-Nonadrenaline Reuptake Inhibitors and is an antidepressant prescribed for the treatment and prevention of relapse of depression. 289280 0
Condition category
Condition code
Other 289604 289604 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 desvenlafaxine (1 x 100 mg) on five occasions and the innovator formulation of desvenlafaxine (1 x 100 mg) on five occasions with each dose seperated by a 10 day washout period.

Each dose (1 x 100 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.

On study days 5 and 19 standard meals will be consumed at the Clinical Site with no additional food intake allowed. Alcohol breath testing will be performed upon each participant reporting to the Clinical Site 10 hours prior to dosing on study days 5 and 19.

Pre and post study laboratory tests will be completed to assess the healthy of participants along with HIV, Hepatitis and drugs of abuse testing.
Intervention code [1] 287257 0
Treatment: Drugs
Comparator / control treatment
Multiple dose, crossover over study design whereby each participant receives the test formulation of desvenlafaxine (1 x 100 mg) on five occasions and the innovator formulation of desvenlafaxine (1 x 100 mg) on five occasions with each dose seperated by a 10 day washout period.
Control group
Active

Outcomes
Primary outcome [1] 289696 0
To compare the bioavailability of O-desmethylvenlafaxine (as summarised by AUC0-t(ss), Cmax(ss) and Cmin(ss)) for the two formulations. All plasma samples will be assayed for O-desmethylvenlafaxine using a fully validated LC/MS/MS method. Validation will be conducted to comply with EU and FDA guidelines.
Timepoint [1] 289696 0
Pre-dose samples on study days 1 to 4 and 15 and 18 and 0, 1, 2, 3, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5, 9.0, 10.0, 11.0, 12.0, 16.0, 20.0 and 24.0 hours on study days 5 and 19
Secondary outcome [1] 303043 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] 303043 0
Pre-dose samples on study days 1 to 4 and 15 and 18 and 0, 1, 2, 3, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5, 9.0, 10.0, 11.0, 12.0, 16.0, 20.0 and 24.0 hours on study days 5 and 19

Eligibility
Key inclusion criteria
Healthy males and Females
Aged between 18 and 55
Non-smoker
BMI between 19 and 30
Normal, healthy individuals as determined by medical history, physical examination, ECG, bood 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
History of depression, anxiety, obsessive-compulsive disorder, or post-traumatic stress syndrome
Pregnant or breast-feeding
Sensitivity to desvenlafaxine, any antidepressant agens, excipients of desvenlafaxine
History of any conditions that might interfere with the absorption, distribution, metabolism or excretion of the drug
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
10/06/2013
Actual
10/06/2013
Date of last participant enrolment
Anticipated
Actual
12/07/2013
Date of last data collection
Anticipated
Actual
Sample size
Target
26
Accrual to date
Final
Recruitment outside Australia
Country [1] 5119 0
New Zealand
State/province [1] 5119 0
Otago

Funding & Sponsors
Funding source category [1] 287371 0
Commercial sector/Industry
Name [1] 287371 0
Actavis Group PTC ehf
Country [1] 287371 0
Ireland
Primary sponsor type
Commercial sector/Industry
Name
Zenith Technology Corporation Limited
Address
156 Frederick Street
Dunedin 9016
Country
New Zealand
Secondary sponsor category [1] 286117 0
None
Name [1] 286117 0
Address [1] 286117 0
Country [1] 286117 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 289346 0
Northern A Health and Disability Ethics Committee
Ethics committee address [1] 289346 0
Ethics committee country [1] 289346 0
New Zealand
Date submitted for ethics approval [1] 289346 0
Approval date [1] 289346 0
10/05/2013
Ethics approval number [1] 289346 0
13/NTA/43

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

Contacts
Principal investigator
Name 40410 0
Dr Noelyn Hung
Address 40410 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 40410 0
New Zealand
Phone 40410 0
+6434779669
Fax 40410 0
Email 40410 0
[email protected]
Contact person for public queries
Name 40411 0
Linda Folland
Address 40411 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 40411 0
New Zealand
Phone 40411 0
+6434779669
Fax 40411 0
Email 40411 0
[email protected]
Contact person for scientific queries
Name 40412 0
Cheung-Tak Hung
Address 40412 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 40412 0
New Zealand
Phone 40412 0
+6434779669
Fax 40412 0
Email 40412 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

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

Documents added automatically
No additional documents have been identified.