TrialSignal
Clinical trial intelligence report
Modular Phase II Study to Link Targeted Therapy to Patients With Pathway Activated Tumors: Module 2 - Dovitinib for Patients With Tumor Pathway Activations Inhibited by Dovitinib Including Tumors With Mutations or Translocations of FGFR, PDGFR, VEGF, cKIT, FLT3, CSFR1, Trk and RET
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01831726-Jul 28, 2026
NCT ID
NCT01831726
Status
COMPLETED
Phase
PHASE2
Sponsor
Novartis Pharmaceuticals
Executive brief
Investment-Ready Snapshot
Modular Phase II Study to Link Targeted Therapy to Patients With Pathway Activated Tumors: Module 2
Dovitinib for Patients With Tumor Pathway Activations Inhibited by Dovitinib Including Tumors With Mutations or Translocations of FGFR, PDGFR, VEGF, cKIT, FLT3, CSFR1, Trk and RET is a PHASE2 clinical asset sponsored by Novartis Pharmaceuticals in Tumor Pathway Activations Inhibited by Dovitinib. SEO and diligence focus: Dovitinib (TKI258), endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01831726
Indication
Tumor Pathway Activations Inhibited by Dovitinib
Modality
small molecule
Target
Dovitinib (TKI258)
Intervention
Dovitinib (TKI258)
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.