This trial is an open, national, multi-centre trial. The main objective of this trial is to assess the tolerability of the up-dosing phase of AVANZ® Cupressus arizonica by measurement of related Adverse Events.
The main objective of this trial is to assess the tolerability of the up-dosing phase of AVANZ® Cupressus arizonica, the measurement rate is the frequency of patients with investigational medicinal product (IMP)-related adverse events (AEs) will be the primary endpoint.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
52
AVANZ Cupressus
Hospital Clinico Universitario San Carlos
Madrid, Madrid, Spain
Frequency of patients with IMP-related AEs
Time frame: 6 treatment weeks
Frequency of patients with systemic reactions
Time frame: 6 weeks of treatment
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