TrialSignal
Clinical trial intelligence report
An Open Label, Phase 1 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Rogaratinib (BAY1163877) in Chinese Patients With FGFR-positive Refractory, Locally Advanced, or Metastatic Solid Tumors
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 17, 2026
NCT ID
NCT03788603
Status
COMPLETED
Phase
Phase 1
Sponsor
Bayer
Executive brief
Investment-Ready Snapshot
Rogaratinib (BAY1163877) is being evaluated for safety and pharmacokinetics in Chinese patients with FGFR-positive refractory, locally advanced, or metastatic solid tumors. The focus on a specific patient population with high FGFR expression levels may position Bayer favorably in the targeted therapy market, particularly in oncology. Given the increasing emphasis on precision medicine, successful outcomes could enhance Bayer's portfolio in the competitive landscape of FGFR inhibitors, which includes other agents currently in development or on the market. The completion of this trial may also provide valuable data for future regulatory submissions and broaden the therapeutic indications for rogaratinib, potentially increasing its market share.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03788603
Indication
Neoplasms
Modality
small molecule
Target
Fibroblast Growth Factor Receptors (FGFR1, 2, 3, 4)
Intervention
Rogaratinib (BAY1163877)
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.