TrialSignal
Clinical trial intelligence report
A Phase 1/2 Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of IMPT-514 in Participants With Active, Refractory Lupus Nephritis and Systemic Lupus Erythematosus
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06153095-Jul 28, 2026
NCT ID
NCT06153095
Status
WITHDRAWN
Phase
PHASE1
Sponsor
Lyell Immunopharma, Inc.
Executive brief
Investment-Ready Snapshot
A Phase 1/2 Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of IMPT-514 in Participants With Active, Refractory Lupus Nephritis and Systemic Lupus Erythematosus is a PHASE1 clinical asset sponsored by Lyell Immunopharma, Inc. in Systemic Lupus Erythematosus, Lupus Nephritis. SEO and diligence focus: IMPT-514, IMPT-514, IMPT-514, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06153095
Indication
Systemic Lupus Erythematosus
Modality
cell therapy
Target
IMPT-514, IMPT-514, IMPT-514
Intervention
IMPT-514, IMPT-514, IMPT-514
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.