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CompletedNCT01042457

Concentration-controlled Therapy of Mycophenolate Mofetil (MMF) in Proliferative Lupus Nephritis

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Chulalongkorn University · Academic / Other
Sex
All
Age
16 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To evaluate therapeutic response to MMF treatment in patients with International Society of Nephrology/Renal Pathology Society (ISN/RPS) class III or IV lupus nephritis. Mycophenolic acid levels at 1-hour post dose will be monitored monthly up to 6 months.

Conditions

Interventions

TypeNameDescription
DRUGMycophenolate mofetilDrug : Mycophenolate Mofetil. Starting doses : 1000-1500 mg/day with titration based on Mycophenolic 1-hour post dose level.

Timeline

Start date
2009-05-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2010-01-05
Last updated
2013-09-30

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT01042457. Inclusion in this directory is not an endorsement.

Concentration-controlled Therapy of Mycophenolate Mofetil (MMF) in Proliferative Lupus Nephritis (NCT01042457) · Clinical Trials Directory