May 19 (Reuters) - Chinook Therapeutics Inc KDNY.O :
* CHINOOK THERAPEUTICS- BION-1301 REMAINS WELL-TOLERATED,
WITH NO
SERIOUS ADVERSE EVENTS AND NO TREATMENT DISCONTINUATIONS DUE TO
ADVERSE EVENTS
* CHINOOK THERAPEUTICS INC - ALL PATIENTS WITH IGAN IN
COHORT 1
HAVE TRANSITIONED TO SUBCUTANEOUS (SC) DOSING
* CHINOOK THERAPEUTICS -DATA FROM TRIAL WILL INFORM DESIGN
OF
PHASE 3 TRIAL OF BION-1301 FOR PATIENTS WITH IGAN THAT CO PLANS
TO INITIATE IN 2023
* CHINOOK THERAPEUTICS - BION-1301 DEMONSTRATED 50%
PROTEINURIA
REDUCTION IN PATIENTS WITH IGAN AFTER THREE TO SIX MONTHS OF
TREATMENT
Source text for Eikon: ID:nGNX3zlm1t
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((Reuters.Brief@thomsonreuters.com;))