Efficacy and Safety in Patients With Primary IgA Nephropathy Who Have Completed Study Nef-301 (Nefigard-OLE)

PHASE3CompletedINTERVENTIONAL
Enrollment

119

Participants

Timeline

Start Date

November 17, 2020

Primary Completion Date

February 26, 2024

Study Completion Date

February 26, 2024

Conditions
Primary IgA Nephropathy
Interventions
DRUG

Nefecon 16mg daily

All study patients received Nefecon 16 mg daily for 9 months.

Trial Locations (18)

94304

13 Investigator sites, Palo Alto

Unknown

4 Investigator sites, Buenos Aires

6 Investigator sites, Melbourne

3 Investigator sites, Minsk

4 Investigator sites, Brussels

7 Investigator sites, Québec

6 Investigator sites, Prague

2 Investigator sites, Jyväskylä

2 Investigator sites, Saint-Priest-en-Jarez

5 Investigator sites, Aachen

5 Investigator sites, Athens

2 Investigator sites, Milan

2 Investigator sites, Lodz

4 Investigator sites, Gyeonggi-do

4 Investigator sites, Barcelona

3 Investigator sites, Uppsala

3 Investigator sites, Kayseri

6 Investigator sites, Leicester

Sponsors
All Listed Sponsors
lead

Calliditas Therapeutics AB

INDUSTRY