Novartis Investigative Site
Mid Glamorgan, Wales, CF484DR, United Kingdom
NCT Number: NCT02245828
This is a double blind, randomized, placebo controlled, single and multiple ascending dose study in healthy subjects. Safety evaluation will include (serious) adverse events, vital signs, body weight and lung function tests. Blood samples for Pharmacokinetics will also be drawn at specified timepoints.
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Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Mid Glamorgan, Wales, CF484DR, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Single and multiple ascending doses of QCC374
Placebo comparator
Time frame: 39 days
Number of Participants with Adverse Events
Time frame: 39 days
Area under the plasma concentration-time curve from time zero to infinity
Time frame: 39 days
The area under the plasma concentration-time curve from time zero to the time of the last quantifiable concentration
Time frame: 39 days
The area under the plasma concentration-time curve from time zero to the end of the dosing interval tau
Time frame: 39 days
The average steady state plasma concentration during multiple dosing
Time frame: 39 days
The observed maximum plasma concentration following drug administration
Time frame: 39 days
The terminal elimination half life
Time frame: 39 days
The time to reach the maximum concentration after drug administration
Novartis Pharmaceuticals
Industry
A Randomized, Double-blind, Placebo-controlled First-in-human Study to Assess the Safety, Tolerability and Pharmacokinetics of Single and Multiple Ascending Doses of QCC374 in Healthy Subjects
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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