Last updated: October 31, 2023
Sponsor: Sanofi
Overall Status: Active - Recruiting
Phase
2
Condition
N/ATreatment
N/AClinical Study ID
TX321918
SFY17915
Ages 18-100 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Participants must be 18 years of age (when signing informed consent form)
- Diagnosis of AD for at least 1 year (defined by the American Academy of Dermatology Consensus Criteria)
- Documented history (within 6 months before screening) of either inadequate response or inadvisability to topical treatments
Exclusion
Exclusion Criteria:
- Skin co-morbidity that would adversely affect the ability to undertake AD assessments
- Receipt of any vaccine (expect influenza and COVID-19 vaccines) within 3 months prior to screening
- Receipt of any pneumococcal vaccine within approximate timeframe of 5 years prior to screening
- Prior receipt of two or more doses of Pneumovax 23 at any time
- Receipt of any tetanus-, diphtheria-, or pertussis-containing vaccine within approximate timeframe of 5 years prior to screening
- Participants for whom administration of the pneumococcal vaccine provided in this study is contraindicated or medically inadvisable, according to local label of the vaccine
- Participants for whom administration of the tetanus, diphtheria, and pertussis vaccine provided in this study is contraindicated or medically inadvisable, according to local label of the vaccine
Study Design
Study Start date:
Estimated Completion Date:
Study Description
Connect with a study center
AMR Fort Myers
Fort Myers, Florida 33912
United StatesActive - Recruiting
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