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Urine Collection (UC)
Version: 1.0
Date Modified: 2024-01-15
Vital Signs (VS)
Version: 1.0
Date Modified: 2024-01-15
Urinalysis (URI)
Version: 1.0
Date Modified: 2024-01-15
Informed Consent (IC)
CDASH
Version: 1.0
Date Modified: 2024-01-15
General Clinical Assessment (GCA)
CDASH
Version: 1.0
Date Modified: 2024-01-15
Patient Questionnaire (PQ)
Version: 1.0
Date Modified: 2024-01-15
Hematology Laboratory Results (HLR)
Version: 1.0
Date Modified: 2024-01-15
Surgical Procedure (SP)
Version: 1.0
Date Modified: 2024-01-15
End-of-Treatment Visit (EV)
Version: 1.0
Date Modified: 2024-01-15
Biopsy Results (BR)
Version: 1.0
Date Modified: 2024-01-15
Protocol Deviation (PD)
Version: 1.0
Date Modified: 2024-01-15
Study Treatment Dosing (STD)
Version: 1.0
Date Modified: 2024-01-15
Serious Adverse Event (SAE)
Version: 1.0
Date Modified: 2024-01-15
Eligibility Checklist (EC)
Version: 1.0
Date Modified: 2024-01-15
Vital Signs Follow-up (VSF)
Version: 1.0
Date Modified: 2024-01-15
Randomization Assignment (RA)
Version: 1.0
Date Modified: 2024-01-15
Drug Administration Record (DAR)
CDASH
Version: 1.0
Date Modified: 2024-01-15
Blinding Integrity (BI)
Version: 1.0
Date Modified: 2024-01-15
Medication Changes (MC)
Version: 1.0
Date Modified: 2024-01-15
Biopsy Results (BR)
Version: 1.0
Date Modified: 2024-01-15
General Clinical Assessment (GCA)
Version: 1.0
Date Modified: 2024-01-15
General Clinical Assessment (GCA)
CDASH
Version: 1.0
Date Modified: 2024-01-15
Study Drug Accountability (SDA)
Version: 1.0
Date Modified: 2024-01-15
Serum Chemistry (SC)
CDASH
Version: 1.0
Date Modified: 2024-01-15
Adverse Event (AE)
Version: 1.0
Date Modified: 2024-01-15
Dispensing and Return (DAR)
Version: 1.0
Date Modified: 2024-01-15
Quality of Life Questionnaire (QOLQ)
Version: 1.0
Date Modified: 2024-01-15