Ongoing Clinical Trials
ONGOING CLINICAL TRIALS
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- A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Safety and Efficacy of CCX168 (Avacopan) in Patients with Anti-Neutrophil Cytoplasmic Antibody (ANCA)- Associated Vasculitis Treated Concomitantly with Rituximab or Cyclophosphamide/Azathioprine
Principal Investigator: Dia R. Waguespack, MDStudy Coordinator: Iram AbbasiEmail: RenalResearch@uth.tmc.eduPhone: 713-500-6820Main Inclusion Criteria: Aged at least 18 years, with newly-diagnosed or relapsed AAV where treatment with Cyclophosphamide or rituximab is needed
- A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Safety and Efficacy of CCX168 (Avacopan) in Patients with Anti-Neutrophil Cytoplasmic Antibody (ANCA)- Associated Vasculitis Treated Concomitantly with Rituximab or Cyclophosphamide/Azathioprine
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- A phase III, randomised, open-label, comparative safety and efficacy trial of intravenous iron isomaltoside (Monofer®) and iron sucrose in subjects with iron deficiency anemia and non-dialysis-dependent chronic kidney disease
Principal Investigator: Dia R. Waguespack, MDStudy Coordinator: Iram AbbasiEmail: RenalResearch@uth.tmc.eduPhone: 713-500-6820Main Inclusion Criteria: >18 years of age
- A phase III, randomised, open-label, comparative safety and efficacy trial of intravenous iron isomaltoside (Monofer®) and iron sucrose in subjects with iron deficiency anemia and non-dialysis-dependent chronic kidney disease
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- A Study to Evaluate the Effect of Dapagliflozin on Renal Outcomes and Cardiovascular Mortality in Patients with Chronic Kidney Disease
Principal Investigator: Dia R. Waguespack, MDStudy Coordinator: Iram AbbasiEmail: RenalResearch@uth.tmc.eduPhone: 713-500-6820Main Inclusion Criteria: >18 years of age
- A Study to Evaluate the Effect of Dapagliflozin on Renal Outcomes and Cardiovascular Mortality in Patients with Chronic Kidney Disease
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- A Randomized, Controlled Double-blind Study Comparing the Efficacy and Safety of Orelvo (voclosporin) (23.7 mg Twice Daily) with Placebo in Achieving Renal Response in Subjects with Active Lupus Nephritis
Principal Investigator: Dia R. Waguespack, MDStudy Coordinator: Iram AbbasiEmail: RenalResearch@uth.tmc.eduPhone: 713-500-6820Main Inclusion Criteria: 18 to 75 years of age
- A Randomized, Controlled Double-blind Study Comparing the Efficacy and Safety of Orelvo (voclosporin) (23.7 mg Twice Daily) with Placebo in Achieving Renal Response in Subjects with Active Lupus Nephritis
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- Pathway Exploration and Analysis in Renal Lupus (PEARL) – Phase 2
Principal Investigator: Dia R. Waguespack, MDStudy Coordinator: Iram AbbasiEmail: RenalResearch@uth.tmc.eduPhone: 713-500-6820Main Inclusion Criteria: >18 years of age
- Pathway Exploration and Analysis in Renal Lupus (PEARL) – Phase 2