A PHASE 2 STUDY TO ASSESS THE EFFICACY AND SAFETY OF INTRAVENOUS INFUSION WITH HUMAN SOLUBLE RECOMBINANT FC-GAMMA RECEPTOR IIB (SM101/ BAX 1810) IN SUBJECTS WITH IMMUNOGLOBULIN A NEPHROPATHY (IGAN)

Registry ID
181501
Source registry
HEALTH_CANADA
Status
Pending
Phase
PHASE2
Study type
INTERVENTIONAL
Sponsor
BAXALTA US INC
Last update
2015-11-06

Conditions

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