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Safety and Efficacy of Polyclonal Antibodies in Simultaneous Pancreas Kidney Transplant Recipients: Single-centre, Prospective, Observational Study
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT03470961-Aug 04, 2026
NCT ID
NCT03470961
Status
UNKNOWN
Phase
Phase 4
Sponsor
Tianjin First Central Hospital
Executive brief
Investment-Ready Snapshot
This study, sponsored by Tianjin First Central Hospital, aims to evaluate the safety and efficacy of two polyclonal antibody regimens in simultaneous pancreas-kidney transplant recipients. The market for immunosuppressive therapies in transplant medicine is significant, with increasing demand for improved outcomes in high-risk patients. The results of this study could position the sponsor favorably against competitors in the immunosuppressive drug market, particularly if non-inferiority is demonstrated. Given the study's observational nature, it may also provide valuable real-world evidence that could enhance market access strategies and inform pricing models. The focus on a specific patient population (end-stage diabetic nephropathy) may also allow for targeted marketing strategies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03470961
Indication
CKD (Chronic Kidney Disease) Stage 5T
Modality
small molecule
Target
Polyclonal antibodies targeting T-lymphocytes, specifically Anti-T-lymphocyte globulins (Grafalon) and Anti-thymocyte globulins (ATG).
Intervention
Anti-Tlymphocyte Globulins, Anti-Thymocyte Globulins
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.