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MT2024-16: A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Activity of Single Ascending Doses of SBT777101 in Subjects with Hidradenitis Suppurativa

Status: Recruiting
This research study is for people who have Hidradenitis Suppurativa (HS) and it is moderate or severe in intensity and have been treated with at least one conventional therapy for HS. This study involves the investigational drug SBT777101, which is created by genetically modifying a patient’s own immune cells. The word “investigational” means that this drug has not been approved by the U.S. Food and Drug Administration (FDA) for marketing. SBT777101 is being developed to treat people with hidradenitis suppurativa (HS).
Sex: Male or Female
Age Group: 18 years and over
Inclusion Criteria:
Diagnosis of Hidradenitis Suppurativa
Exclusion Criteria:
History of Crohns diseaseInterventions:
Biological: SBT777101
Conditions:
Dermatology (Skin, Hair & Nails)
Keywords:
Clinics and Surgery Center (CSC), Hidradenitis suppurativa
Study Contact: Irmina Wallander - wall0396@umn.edu
Principal Investigator: Noah Goldfarb
Phase: PHASE1
IRB Number: STUDY00021432
See this study on ClinicalTrials.gov