About this trial
The main purpose of this study is to evaluate the safety and tolerability of IBI3005 and to determine the maximum tolerated dose (MTD) and the recommended Phase 2 Dose (RP2D) of IBI3005.
Eligibility criteria
Qualifiers
None
Disqualifiers
Infection requiring systemic antibiotics, antivirals or antifungals within 2 weeks prior to first dose of the study drug( antiviral medication for hepatitis B and hepatitis C infection that are compliant with the protocol were allowed);
Known human immunodeficiency virus (HIV) infection, or HIV positive (HIV 1/2 Ab positive);
Acute or chronic active hepatitis B (HbsAg positive and/or HbcAb positive with HBV DNA titer ≥ 104 copies/mL or ≥ 2000 IU/mL or higher than lower limit of detection) or C (HCV Ab positive with HCV RNA titer > 103 copies/mL or higher than lower limit of detection);
Active COVID-19 infection with obvious symptoms requiring treatment or hospitalization, such as pyrexia, dyspnea, nausea, vomiting, diarrhea, etc.;
Trial design
Treatments tested in this trial
- IBI3005