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A Phase 1, Open-Label, Non-Randomized, Dose-Finding, Safety and Tolerability Study of Orally Administered Teysuno (S-1) in Combination With Epirubicin and Oxaliplatin in Patients With Advanced Solid Tumors
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02867397-Jul 28, 2026
NCT ID
NCT02867397
Status
COMPLETED
Phase
Phase 1
Sponsor
Disphar International B.V.
Executive brief
Investment-Ready Snapshot
Disphar International B.V. is exploring the combination of Teysuno (S-1), a known oral chemotherapy agent, with epirubicin and oxaliplatin in patients with advanced solid tumors. The Phase 1 trial aims to establish the maximum tolerated dose (MTD) and assess safety and tolerability. Given the lack of established curative therapies for advanced solid tumors, this combination therapy could address a significant unmet medical need. The competitive landscape includes existing therapies for advanced solid tumors, but the unique oral formulation of S-1 may provide a differentiated offering. Diligence should focus on the safety profile and potential market acceptance of this combination therapy, especially in regions where oral chemotherapy is preferred.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02867397
Indication
Patients With Advanced or Metastatic Solid Tumors
Modality
combination therapy
Target
Oral administration of Teysuno (S-1) in combination with epirubicin and oxaliplatin targeting advanced solid tumors.
Intervention
Teysuno (S1) in combination with epirubicin and oxaliplatin
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.