BIIX 1 XX inhalation solution
Drugsingle doses of 800, 1000, 1200, 1400, 1600, 1800, or 2000 mcg
NCT Number: NCT02198287
Safety, tolerability and pharmacokinetic study of BIIX 1 XX in healthy male volunteers.
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Notify Me21 year–50 year
Male
Interventional
Phase 1
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
single doses of 800, 1000, 1200, 1400, 1600, 1800, or 2000 mcg
Time frame: up to 22 days
Time frame: up to 8 days after drug administration
Time frame: up to 8 days after drug administration
Time frame: pre-dose, 10 and 30 minutes after administration
Time frame: pre-dose, 10 and 30 minutes after administration
Time frame: up to 8 days after drug administration
Time frame: up to 168 hours after drug administration
Time frame: up to 168 hours after drug administration
Time frame: up to 168 hours after drug administration
Time frame: up to 168 hours after drug administration
Boehringer Ingelheim
Industry
A Single Increasing Dose Safety and Tolerability Study (Dose Extension) After Inhalational Administration of BIIX 1 XX (Single Doses: 800 - 2000 mcg) in Healthy Young Male Volunteers (Randomised, Double-blind, Placebo-controlled)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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