Status and phase
Conditions
Treatments
About
The study will look at whether it is preferable to administer two wafers simultaneously or separately.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Males or females aged 18-65 years.
Good general health without clinically significant renal, hepatic, cardiac or respiratory disease, as determined by the Principal Investigator.
Willing and able to give informed consent and agree to complete all study procedures.
Have suitable venous access for blood sampling.
Female participants are eligible only if all the following apply:
BMI within the range of 19-30 kg/m2 (inclusive).
Deemed able to read and understand English in order to communicate with research staff and complete protocol required questionnaires and forms.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
10 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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