MIRACLE Study: A Study of Once-Monthly Intravenous Mircera in Hemodialysis Participants With Chronic Renal Anemia

PHASE3CompletedINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

October 31, 2009

Study Completion Date

October 31, 2009

Conditions
Anemia
Interventions
DRUG

Methoxy polyethylene glycol-epoetin beta

Mircera will be administered intravenously every 4 weeks for a total of 52 weeks. The first dose of 120, 200, or 360 mcg will be determined by the dose of ESA received prior to administration of study treatment, while subsequent doses will be adjusted to maintain hemoglobin within a country-specific target range.

Trial Locations (27)

1011

Lausanne

1030

Vienna

1100

Vienna

1130

Vienna

1160

Vienna

1205

Geneva

1220

Vienna

1951

Sion

3100

Sankt Pölten

3400

Burgdorf

4020

Linz

4031

Basel

4400

Steyr

4410

Liestal

5020

Salzburg

6004

Lucerne

6330

Kufstein

6500

Bellinzona

6600

Locarno

6807

Feldkirch

6850

Mendrisio

6900

Bregenz

6903

Lugano

8020

Graz

8037

Zurich

8091

Zurich

9007

Sankt Gallen

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT00545571 - MIRACLE Study: A Study of Once-Monthly Intravenous Mircera in Hemodialysis Participants With Chronic Renal Anemia | Biotech Hunter | Biotech Hunter