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 20, 2026
NCT ID
NCT03788603
Status
COMPLETED
Phase
Phase 1
Sponsor
Bayer
Executive brief
Investment-Ready Snapshot
Rogaratinib (BAY1163877) is being evaluated in a Phase 1 clinical trial targeting FGFR-positive refractory, locally advanced, or metastatic solid tumors in Chinese patients. Given the increasing prevalence of FGFR mutations in various cancers, this asset has the potential to address a significant unmet medical need in oncology. The trial's completion in April 2020 positions Bayer to leverage the data for potential regulatory submissions or partnerships, particularly in the Asian market where FGFR-targeted therapies are underrepresented. Competitive analysis indicates that while there are existing FGFR inhibitors, the unique pharmacokinetic profile of rogaratinib may provide a differentiated therapeutic option. Diligence should focus on the safety and tolerability data, as well as the pharmacokinetic outcomes, to assess the viability for further development or commercialization.
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.