This open-label Phase 2 study will characterize the safety and efficacy of JADE101 in participants with IgA nephropathy, and the results will contribute to the overall clinical characterization of JADE101 in this patient population.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
JADE101 is supplied as sterile solution to be administered by SC injection
Jade Clinical Site
Chula Vista, California, United States
RECRUITINGJade Clinical Site
Arvada, Colorado, United States
Incidence of treatment-emergent adverse events (safety and tolerability)
The proportion of participants who experience one or more adverse events that begin or worsen after the first dose of study drug
Time frame: Day 1 through 100 weeks
Effect of JADE101 on Urine Protein Creatinine Ratio (UPCR) in participants with IgA nephropathy
Change from baseline in UPCR
Time frame: Day 1 through 100 weeks
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Jade Clinical Site
Denver, Colorado, United States
RECRUITINGJade Clinical Site
Orlando, Florida, United States
RECRUITINGJade Clinical Site
Pembroke Pines, Florida, United States
RECRUITINGJade Clinical Site
Houston, Texas, United States
RECRUITINGJade Clinical Site
Concord, New South Wales, Australia
RECRUITINGJade Clinical Site
Christchurch, New Zealand
RECRUITINGJade Clinical Site
Anyang-si, South Korea
RECRUITINGJade Clinical Site
Seongnam-si, South Korea
RECRUITING...and 5 more locations