A Study of OL-108 in Relapsed/Refractory Autoimmune Diseases

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBeijing GoBroad Hospital

About this trial

This study aims to characterize the safety, tolerability, pharmacokinetics, and preliminary efficacy of OL-108 in relapsed/refractory autoimmune diseases.

Eligibility criteria

Qualifiers

Adults aged 18-65 years old

ECOG 0-2

Adequate organ function

Females of childbearing potential (FCBP) must have a negative pregnancy test at screening and must agree to use a highly effective contraceptive method starting from the time of lymphodepletion and for 2 years after dosing of the IMP

Disqualifiers

Active uncontrolled infection

Serologic evidence of chronic hepatitis B virus (HBV) infection and unable or unwilling to receive standard prophylactic antiviral therapy or with detectable HBV viral load

Serologic evidence of hepatitis C virus (HCV) infection without completion of curative treatment or with detectable HCV viral load

HIV antibody positive

Trial design

Treatments tested in this trial

  • OL-108

Treatment groups

44 Participants
are divided into 1 treatment group

Sponsors and collaborators