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Clinical trial intelligence report
Investigation of the Pharmacokinetics of Subcutaneously Administered NNC0480-0389 in Participants With Various Degrees of Impaired Renal Function Compared to Participants With Normal Renal Function
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT05015894-Jul 28, 2026
NCT ID
NCT05015894
Status
COMPLETED
Phase
Phase 1
Sponsor
Novo Nordisk A/S
Executive brief
Investment-Ready Snapshot
Novo Nordisk is advancing NNC0480-0389 as a potential combination therapy for T2D, targeting a significant patient population with renal impairment, which is often underserved in diabetes management. The study's focus on pharmacokinetics in patients with impaired renal function positions the asset favorably in a competitive landscape where renal safety and efficacy are critical. The successful completion of this trial may enhance Novo Nordisk's portfolio in diabetes care, particularly in the context of increasing prevalence of T2D and associated renal complications. The market for diabetes therapies is substantial, with a growing demand for innovative solutions that address the complexities of comorbid conditions.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05015894
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
NNC0480-0389, a novel investigational agent, is designed to enhance blood sugar control in type-2 diabetes (T2D) patients, particularly those with varying degrees of renal impairment, in combination with semaglutide.
Intervention
NNC0480-0389
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.