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
Evaluate 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
Doral, Florida, United States
RECRUITINGADARx Clinical Site
Miami, Florida, United States
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Pembroke Pines, Florida, United States
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Iowa City, Iowa, United States
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Shreveport, Louisiana, United States
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Shelby, Michigan, United States
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Great Neck, New York, United States
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Columbus, Ohio, United States
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Dakota Dunes, South Dakota, United States
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Dallas, Texas, United States
RECRUITING...and 19 more locations