Study to assess safety and tolerability of a single dose of study-drug administered to Cystic Fibrosis (CF) patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
25
A single nominal dose of CR002 (three different dose groups) will be inhaled as an aerosol mist produced by an I-neb Adaptive Aerosol Delivery (AAD) System.
A single nominal dose of Placebo will be inhaled as an aerosol mist produced by an I-neb Adaptive Aerosol Delivery (AAD) System.
Site 11
Sofia, Bulgaria
Site 12
Varna, Bulgaria
Site 30
Debrecen, Hungary
Site 24
Bialystok, Poland
Frequency of Adverse events
Time frame: 44 Days (Day -21 to Day 22)
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Site 22
Gdansk, Poland
Site 21
Poznan, Poland
Site 20
Rabka-Zdrój, Poland
Site 23
Warsaw, Poland
Site 42
Papworth Hospital, United Kingdom
Site 40
Penarth, United Kingdom
...and 1 more locations