This Phase 2 study is designed to assess the safety, efficacy, pharmacokinetics (PK) and pharmacodynamics (PD) of ADX-038 in adults with complement-mediated kidney diseases.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
45
siRNA duplex oligonucleotide
siRNA duplex oligonucleotide
ADARx Clinical Site
Shreveport, Louisiana, United States
RECRUITINGADARx Clinical Site
Shelby, Michigan, United States
RECRUITINGEvaluate the safety and tolerability of ADX-038
Incidence and severity of TEAEs
Time frame: Length of study - 36 months
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ADARx Clinical Site
Dakota Dunes, South Dakota, United States
RECRUITINGADARx Clinical Site
Dallas, Texas, United States
RECRUITINGADARx Clinical Site
Houston, Texas, United States
RECRUITINGADARx Clinical Site
Wollongong, New South Wales, Australia
RECRUITINGADARx Clinical Site
Pok Fu Lam, Hong Kong
RECRUITINGADARx Clinical Site
Shatin, Hong Kong
RECRUITINGADARx Clinical Site
Gyeonggi-do, New South Wales, South Korea
RECRUITINGADARx Clinical Site
Seoul, New South Wales, South Korea
RECRUITING...and 2 more locations