None listed
Conditions
Brief summary
The objective of this study is to evaluate the bioequivalence of the test (new) formulation of 1 x 100 mg against the reference formulation (innovator brand of 1 x 100 mg modafinil tablet) following oral administration of a single dose of 1 x 100 mg in healthy male and female subjects under fasting conditions.
Interventions
Single dose, crossover study design whereby each participant receives the test formulation of modafinil (1 x 100 mg) on one occasion and the innovator formulation of modafinil (1 x 100 mg) on one occasion with each dose seperated by a one week washout period. The intervention for this trial is the test formulation of modafinil.
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 hour
Single dose, crossover study design whereby each participant receives the test formulation of modafinil (1 x 100 mg) on one occasion and the innovator formulation of modafinil (1 x 100 mg) on one occasion with each dose seperated by a one week washout period. The intervention for this trial is the test formulation of modafinil. 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 and will be monitored 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 health of participants along with HIV, Hepatitis and drugs of abuse testing. 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.
Sponsors
Zenith Technology Corp Ltd
Study design
Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
All
Age
20 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
Healthy male and non-pregnant females Aged between 20 and 55 Non-smoker BMI between 18 and 33 inclusive Normal, healthy individuals as determined by medical history, physical examination, ECG, blood pressure and laboratory tests
Exclusion criteria
Any history of recent recurrent attacks of bronchitis, asthma, migraine headaches Concomitant drug therapy of any kind Who have received an investigational compound or drug known to induce or inhibit liver enzymes within 60 days of the start of the study Sensitivity to modafinil or any other similar class of medicines, or the excipients of modafinil History of any conditions that might interfere with the absorption, distribution, metabolism or excretion of the drug Females who are pregnant and/or are breastfeeding Who are planning to start a family within 60 days of receiving the final dose. 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
Outcome results
None listed