The purpose of the study is to evaluate the safety and tolerability of the drug product at each dose level.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
22
Unnamed facility
London, United Kingdom
Incidence and severity of adverse events
Time frame: Up to 6 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.