An Open-Label Extension Study of GSK3511294 (Depemokimab) in Participants Who Were Previously Enrolled in 206713 (NCT04719832) or 213744 (NCT04718103)
Completed · Phase 3
Conditions studied: Asthma
In brief
The purpose of this open-label 12-month extension study is to continue to characterize the long-term safety, efficacy and immunogenic profile of GSK3511294 (Depemokimab) in participants with severe asthma with an eosinophilic phenotype following completion of clinical studies 206713 or 213744.
Key facts
- Study ID
- NCT05243680
- Run by
- GlaxoSmithKline
- People needed
- 641
- Starts
- 2022-03-01
- Expected to finish
- 2025-05-19
- Last updated by the study team
- 2026-01-15
Who can join
Age: 12 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participants who completed the double-blind study intervention treatment during Study 206713 or Study 213744.
- Participants capable of giving signed informed consent/assent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol. In France, a participant will be eligible for inclusion in this study only if either affiliated to or a beneficiary of a social security category.
You may not qualify if…
- Clinically significant change in health status during Study 206713 or Study 213744 which in the opinion of the investigator would make the participant unsuitable for participation in this study.
- A current malignancy or a malignancy that developed during Study 206713 or Study 213744 (participants who had localized carcinoma of the skin that was resected for cure will not be excluded).
- Participants who have other clinically significant medical conditions uncontrolled with Standard of Care (SoC) therapy not associated with Asthma, for example (e.g.), uncontrolled cardiovascular disease or ongoing active infectious disease which in the opinion of the investigator makes them unsuitable for the study.
- Participants with known parasitic (helminth) infections within 6 months prior to Visit 1 will be excluded from the study or required to be adequately treated for helminth infections before initiation of GSK3511294.
- Participants who meet the following based on results of Week 48 assessment from Study 206713 or Study 213744 or from a later result:
- Alanine aminotransferase (ALT) greater than (>)2 times upper limit of normal (ULN).
- Total bilirubin >1.5 times ULN (isolated bilirubin >1.5 times ULN is acceptable if bilirubin is fractionated and direct bilirubin less than [<] 35 percent [%]).
- Cirrhosis or current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, persistent jaundice.
- Participants with current diagnosis of vasculitis. Participants with high clinical suspicion of vasculitis at screening will be evaluated and current vasculitis must be excluded prior to enrolment.
- Electrocardiogram (ECG) assessment: QTc corrected by Fridericia's formula (QTcF) greater than or equal to (>=)450 milliseconds (msec) or QTcF >=480 msec for participants with Bundle Branch Block at Visit 1.
- Current smokers.
- Participants with allergy/intolerance to the excipients of GSK3511294, a monoclonal antibody, or biologic.
- Participants who are pregnant or breastfeeding. Participants should not be enrolled if they plan to become pregnant during the time of study participation.
- Participants who for any reason permanently discontinued study treatment in the previous study 206713/213744 will be excluded from this study.
- Other investigational product/clinical study:
- Participants who have received treatment with an investigational agent (biologic or non-biologic) within the past 30 days or 5 drug half-lives whichever is longer, prior to the first dose, other than Study 206713/213744 study treatment. The term "investigational" applies to any drug not approved for sale for the disease/indication to treat in the country in which it is being used or investigational formulations of marketed products.
- Participants who are currently participating in any other interventional clinical study.
Where it is running
- GSK Investigational Site — Lancaster, California, United States
- GSK Investigational Site — Colorado Springs, Colorado, United States
- GSK Investigational Site — Lafayette, Colorado, United States
- GSK Investigational Site — Coral Gables, Florida, United States
- GSK Investigational Site — Hialeah, Florida, United States
- GSK Investigational Site — Loxahatchee Groves, Florida, United States
- GSK Investigational Site — Miami, Florida, United States
- GSK Investigational Site — Miami, Florida, United States
- GSK Investigational Site — Miami, Florida, United States
- GSK Investigational Site — Orlando, Florida, United States
- GSK Investigational Site — Savannah, Georgia, United States
- GSK Investigational Site — Normal, Illinois, United States
- GSK Investigational Site — Lexington, Kentucky, United States
- GSK Investigational Site — Ypsilanti, Michigan, United States
- GSK Investigational Site — Szigetvár, Hungary
- GSK Investigational Site — Brescia, Italy
- GSK Investigational Site — Foggia, Italy
- GSK Investigational Site — Messina, Italy
- GSK Investigational Site — Milan, Italy
- GSK Investigational Site — Northfield, New Jersey, United States
- GSK Investigational Site — Toms River, New Jersey, United States
- GSK Investigational Site — The Bronx, New York, United States
- GSK Investigational Site — Gastonia, North Carolina, United States
- GSK Investigational Site — Huntersville, North Carolina, United States
- GSK Investigational Site — Mobile, Alabama, United States
Full record on ClinicalTrials.gov
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