A PHASE 2, OPEN-LABEL, MULTIPLE DOSE STUDY TO EVALUATE THE PHARMACODYNAMIC EFFECTS, SAFETY AND TOLERABILITY OF PATIROMER FOR ORAL SUSPENSION IN CHILDREN AND ADOLESCENTS 2 TO < 18 YEARS OF AGE WITH CHRONIC KIDNEY DISEASE AND HYPERKALEMIA (EMERALD)

Registry ID
RLY5016-206P
Source registry
HEALTH_CANADA
Status
Ongoing
Phase
PHASE2
Study type
INTERVENTIONAL
Sponsor
VIFOR PHARMA, INC.
Start date
2018-06-14
Last update
2017-04-25

Conditions

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