Trial Review

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The ANZCTR now automatically displays published trial results and simplifies the addition of trial documents such as unpublished protocols and statistical analysis plans.

These enhancements will offer a more comprehensive view of trials, regardless of whether their results are positive, negative, or inconclusive.

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Trial registered on ANZCTR


Registration number
ACTRN12613001123730
Ethics application status
Approved
Date submitted
8/10/2013
Date registered
9/10/2013
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 levonorgestrel tablet against the innovator levonorgestrel tablet conducted under fasting conditions in healthy female volunteers
Scientific title
A single dose, randomized, blinded, bioequivalence study of levonorgestrel tablets in a 2 way crossover comparison against the innovator levonorgestrel tablet conducted under fasting conditions in healthy female volunteers
Secondary ID [1] 283367 0
None
Universal Trial Number (UTN)
U1111-1146-4689
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Bioequivalence study conducted in healthy volunteers comparing two formulations of levonorgestrel 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, levonorgestrel is a progestogen only contraceptive agent.

 290268 0
Condition category
Condition code
Other 290656 290656 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
Single dose, crossover over study design whereby each participant receives the test formulation of levonorgestrel (1 x 1.5 mg) on one occasion and the innovator formulation of levonorgestrel(1 x 1.5 mg) on one occasion with each dose seperated by a two week washout period. The intervention for this trial is the test formulation of levonorgestrel.

Each dose (1 x 1.5 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.

No water is allowed for 1 hour prior to dosing until 1 hour after dosing (except for the water consumed with the dose).

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

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.

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] 288095 0
Treatment: Drugs
Comparator / control treatment
Single dose, crossover over study design whereby each participant receives the test formulation of levonorgestrel (1 x 1.5 mg) on one occasion and the innovator formulation of levonorgestrel (1 x 1.5 mg) on one occasion with each dose seperated by a two week washout period. The comparator/control for this trial is the innovator formulation of levonorgestrel.
Control group
Active

Outcomes
Primary outcome [1] 290674 0
To compare the bioavailability of levonorgestrel (as summarised by Cmax and AUC) for the two formulations. All plasma samples will be assayed for levonorgestrel using a fully validated LC/MS/MS method. Validation will be conducted to comply with EU and FDA guidelines.
Timepoint [1] 290674 0
0, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10.0, 12.0, 16.0, 20.0, 24.0, 32.0, 48.0, 56.0 and 72.0 hours
Secondary outcome [1] 305015 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] 305015 0
0, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10.0, 12.0, 16.0, 20.0, 24.0, 32.0, 48.0, 56.0 and 72.0 hours

Eligibility
Key inclusion criteria
Healthy 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, bood pressure and laboratory tests
Not currently using any prescribed hormonal contraceptives
Able to provide written informed consent
Minimum age
18 Years
Maximum age
55 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Males
Any history of recent recurrent attacks of bronchitis, asthma, migraine headaches
Concomitant drug therapy of any kind
History of any conditions that might interfere with the absorption, distribution, metabolism or excretion of the drug
History of alcohol or drug abuse or dependency
Smoker (anyone who has smoked in the last 6 months)
Participation in a drug study within 60 days of the start of the study or donated blood in the 60 days preceding the study.
Who are pregnant, breastfeeding or who have any obstetric or gynaecological condition
Who have ever had an ectopic pregnancy or have a history or family history of thrombophilia or breast cancer
Sensitivity to levonorgestrel, any contraceptive agents, excipients of levonorgestrel
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
15/10/2013
Actual
30/10/2013
Date of last participant enrolment
Anticipated
Actual
15/01/2014
Date of last data collection
Anticipated
Actual
Sample size
Target
24
Accrual to date
Final
Recruitment outside Australia
Country [1] 5487 0
New Zealand
State/province [1] 5487 0
Otago

Funding & Sponsors
Funding source category [1] 288097 0
Commercial sector/Industry
Name [1] 288097 0
Medigen Pharma Pty Ltd
Country [1] 288097 0
Australia
Primary sponsor type
Commercial sector/Industry
Name
Zenith Technology Corp Ltd
Address
156 Frederick St
Dunedin 9016
Country
New Zealand
Secondary sponsor category [1] 286817 0
None
Name [1] 286817 0
Address [1] 286817 0
Country [1] 286817 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 290020 0
Central Health and Disability Ethics Committee
Ethics committee address [1] 290020 0
Ministry of Health
1 the Terrace
PO Box 5013
Wellington 6145
Ethics committee country [1] 290020 0
New Zealand
Date submitted for ethics approval [1] 290020 0
Approval date [1] 290020 0
05/09/2013
Ethics approval number [1] 290020 0
13/CEN/110

Summary
Brief summary
The objective of this study is to evaluate the bioequivalence of the test (new) formulation of 1.5 mg levonorgestrel tablet relative to that of the reference formulation (innovator brand of 1.5 mg levonorgestrel tablet) following oral administration of a single dose of 1.5 mg in healthy female subjects under fasting conditions.
Trial website
Trial related presentations / publications
No presentations or citations available. Final CSR provided to Sponsor Company for Registration Purposes
Public notes

Contacts
Principal investigator
Name 43514 0
Dr Noelyn Hung
Address 43514 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 43514 0
New Zealand
Phone 43514 0
+6434779669
Fax 43514 0
Email 43514 0
[email protected]
Contact person for public queries
Name 43515 0
Linda Folland
Address 43515 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 43515 0
New Zealand
Phone 43515 0
+6434779669
Fax 43515 0
Email 43515 0
[email protected]
Contact person for scientific queries
Name 43516 0
Cheung-Tak Hung
Address 43516 0
Zenith Technology Corporation Limited 156 Frederick Street (PO Box 1777) Dunedin 9016
Country 43516 0
New Zealand
Phone 43516 0
+6434779669
Fax 43516 0
Email 43516 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
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