Trial ID: | L0146 |
Source ID: | NCT05515367
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Associated Drug: |
Desidustat
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Title: |
A Post Marketing Surveillance to Evaluate the Safety of Desidustat for the Treatment of Anemia in Subjects With Chronic Kidney Disease (CKD).(Real World Evidence Study)
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Acronym: |
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Status: |
RECRUITING
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Study Results: |
NO
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Results: |
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Conditions: |
Chronic Kidney Diseases|Anemia of Chronic Kidney Disease
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Interventions: |
DRUG: Desidustat
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Outcome Measures: |
Primary: To asses the Proportion of Subjects with treatment emergent adverse events., Baseline (week 0) to Week 52 (end of treatment)|To asses the Proportion of Subjects with treatment emergent Serious adverse events., Baseline (week 0) to Week 52 (end of treatment) | Secondary: Mean change in hemoglobin level, Baseline (week 0) to Week 52 (end of treatment)|Mean change in Lipid profile including Small dense LDL from baseline, Baseline (week 0) to Week 52 (end of treatment)|Mean change in VEGF, Baseline (week 0) to Week 52 (end of treatment)|Mean change in serum Hepcidin, Baseline (week 0) to Week 52 (end of treatment)
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Sponsor/Collaborators: |
Sponsor: Zydus Lifesciences Limited
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE4
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Enrollment: |
1004
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
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Start Date: |
2023-04-20
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Completion Date: |
2025-11-30
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Results First Posted: |
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Last Update Posted: |
2025-01-22
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Locations: |
Indira Gandhi Institute of Medical Sciences, Sheikhpura, Bihar, 800014, India
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URL: |
https://clinicaltrials.gov/show/NCT05515367
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