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Clinical trial intelligence report
A First-in-patient Phase I/II Clinical Study to Investigate the Safety, Tolerability and Efficacy of Genome-edited Hematopoietic Stem and Progenitor Cells in Subjects With Severe Complications of Sickle Cell Disease
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT04443907-Aug 04, 2026
NCT ID
NCT04443907
Status
TERMINATED
Phase
PHASE1
Sponsor
Novartis Pharmaceuticals
Executive brief
Investment-Ready Snapshot
A First-in-patient Phase I/II Clinical Study to Investigate the Safety, Tolerability and Efficacy of Genome-edited Hematopoietic Stem and Progenitor Cells in Subjects With Severe Complications of Sickle Cell Disease is a PHASE1 clinical asset sponsored by Novartis Pharmaceuticals in Sickle Cell Disease. SEO and diligence focus: OTQ923, OTQ923, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04443907
Indication
Sickle Cell Disease
Modality
protein therapy
Target
OTQ923, OTQ923
Intervention
OTQ923, OTQ923
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.