SelK2 (Part 1)
DrugI.V., multiple-dose (Day 1 and Day 22)
NCT Number: NCT04540042
This study has two parts. The main purpose of Part 1 of this study will be to examine how safe and effective two doses of SelK2 is on participants with mild asthma. Lung function and inflammatory cell numbers will be measured in response to the administration of an allergen (a compound to which the participant is allergic) into the lungs in the presence or absence of SelK2. Part 2 of this study will examine how safe and effective one dose of SelK2 is on participants with chronic obstructive pulmonary disease (COPD). Lung function and inflammatory cell numbers will be measured in COPD patients in the presence or absence of SelK2. SelK2 may block the movement of key inflammatory cells into the lungs and consequently improve lung function in these two patient populations.
Looking for future studies?
Notify Me18 year–75 year
All sexes
Interventional
Phase 2
Queen Anne Street Medical Centre, London, United Kingdom
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Part 1:
Key Inclusion Criteria
Key Exclusion Criteria
Part 2:
Key Inclusion Criteria
Key Exclusion Criteria
I.V., multiple-dose (Day 1 and Day 22)
I.V., multiple-dose (Day 1 and Day 22)
I.V., single-dose (Day 1)
I.V., single-dose (Day 1)
Time frame: Pre-challenge to between 3 and 8 hours after administration of allergen inhalation challenge
Time frame: Change from baseline to Day 22
Time frame: Pre-challenge to between 3 and 8 hours after administration of allergen inhalation challenge
Time frame: Change from baseline to 8 and 24 hours post allergen challenge
Time frame: Pre-challenge to between 0 and 2 hours after the administration of allergen inhalation challenge
Time frame: Pre-challenge to between 0 and 8 hours after the administration of allergen inhalation challenge
Time frame: Change from baseline to Day 29
Time frame: Change from baseline to Days 4, 8, 15, and 29
Time frame: Change from baseline to Days 4, 8, 15, 22, and 29
Time frame: Change from baseline to Days 4, 8, 15, 22, and 29
Time frame: Change from baseline to Days 4, 8, 15, 22, and 29
Time frame: Change from baseline to Days 4, 8, 15, 22, and 29
Time frame: Change from baseline to Days 4, 8, 15, 22, and 29
Scores range from 0-40 with 40 being associated with the worst outcome.
Time frame: Change from baseline to Days 4, 8, 15, 22, and 29
Scores range from 0-12 with 12 being associated with the worst outcome.
Tetherex Pharmaceuticals Corporation
Industry
A Two Part, Randomised, Double-blind, Placebo-controlled, Phase 2 Parallel Group Study to Evaluate the Safety and Efficacy of Intravenously-Administered SelK2 on Airway Responses Following Allergen Challenge in Subjects With Asthma (Part 1) and to Evaluate the Safety and Efficacy of Intravenously-Administered SelK2 in Subjects With Chronic Obstructive Pulmonary Disease (Part 2)
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.
Published trials that share one or more normalized conditions with this study.
NCT05830318
Asthma, Behavior
Leicester, United Kingdom
View Trial DetailsNCT04849312
Anticoagulants; Increased, Asthma
Boston, Massachusetts, United States
View Trial DetailsNCT05045742
Anticoagulants; Increased, Asthma
Boston, Massachusetts, United States
View Trial DetailsNCT05256303
Anticoagulation, Asthma
Quincy, Illinois, United States
View Trial Details