Status:
COMPLETED
Safety And Efficacy Study Of Orally Administered DS102 In Patients With Chronic Obstructive Pulmonary Disease
Lead Sponsor:
Afimmune
Conditions:
Chronic Obstructive Pulmonary Disease
Eligibility:
All Genders
40-75 years
Phase:
PHASE2
Brief Summary
The purpose of this randomised, double-blind, placebo-controlled, parallel group study is to assess the safety and efficacy of orally administered DS102 capsules versus placebo in the treatment of adu...
Eligibility Criteria
Inclusion
- Patients (male or female) aged 40-75 years with stable COPD at the time of screening.
- Patients who are current or ex-smokers who have a smoking history of at least 10 pack years (Ten pack- years are defined as 20 cigarettes a Day for 10 years, or 10 cigarettes a Day for 20 years).
- Patients whose pre-study clinical laboratory findings do not interfere with their participation in the study, in the opinion of the Investigator.
- Patients who are able to communicate well with the Investigator, to understand and comply with the requirements of the study, and understand and sign the written informed consent.
Exclusion
- Patients with a history of malignancy of any organ system (including lung cancer), treated or untreated, within the past 5 years whether or not there is evidence of local recurrence or metastases, with the exception of localized basal cell carcinoma of the skin.
- Patients with significant systemic or major illness other than pulmonary disease, including coronary artery disease, liver disease, cerebrovascular disease, renal insufficiency, serious psychiatric disease, respiratory or hypertensive disease, as well as diabetes and arthritis that, in the opinion of the Investigator, would preclude the patient from participating in and completing the study.
- Patients with known hypersensitivity to any ingredients of the study treatment.
- Patients, in the opinion of the Investigator, not suitable to participate in the study
Key Trial Info
Start Date :
September 24 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 29 2019
Estimated Enrollment :
49 Patients enrolled
Trial Details
Trial ID
NCT03414541
Start Date
September 24 2017
End Date
January 29 2019
Last Update
January 31 2020
Active Locations (3)
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1
UK Site 2
Belfast, United Kingdom
2
UK Site 3
London, United Kingdom
3
UK Site 1
Manchester, United Kingdom