Clinical trial · Interventional
An Exploratory Clinical Study of SHR6390 and SHR1020 in the Treatment of Esophageal Squamous Cell Carcinoma After Progression on PD-1 Antibody
NCT04866381CI-TRIAL-00051526unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study is being conducted to explore the efficacy of SHR-6390 and SHR-1020 in the treatment of esophageal squamous cell carcinoma after progression on PD-1 Antibody.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Esophageal Squamous Cell Carcinoma | Esophageal Squamous Cell Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Progression to PD-1 Antibody | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Camrelizumab (SHR-1210) + SHR-1020 | Drug | — | UNRESOLVED |
| SHR-6390 | Drug | — | UNRESOLVED |
| SHR-6390 + Camrelizumab (SHR-1210) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- SHR-6390
- description
- SHR-6390
- interventionNames
- Drug: SHR-6390
- type
- EXPERIMENTAL
- label
- SHR-6390 combined with Camrelizumab (SHR-1210)
- description
- SHR-6390 combined with Camrelizumab (SHR-1210)
- interventionNames
- Drug: SHR-6390 + Camrelizumab (SHR-1210)
- type
- EXPERIMENTAL
- label
- Camrelizumab (SHR-1210) combined with SHR-1020
- description
- Camrelizumab (SHR-1210) combined with SHR-1020
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Patients who were diagnosed as esophageal squamous cell carcinoma by histopathology with at least one measurable lesion according to RECIST 1.1 criteria. * Must have had progressive disease after previous treatment with PD-1 inhibitor * ECOG score 0-2 * The expected survival time is ≥ 12 weeks * Previous permanent discontinuation did not occur due to adverse events associated with immunotherapy, or the immunotreatment-related adverse events recovered to ≤1 grade Exclusion Criteria: * Had other active malignant tumors within 5 years before entering the study * Had abnormal swallowing function or dysfunction of gastrointestinal absorption * The first study drug treatment was less than 28 days or 5 half-lives (in terms of longer) from the last radiotherapy, chemotherapy, targeted therapy or immunotherapy * Patients who have already received surgery within 28 days (biopsy for diagnosis is permitted) * Pregnant or lactating women
References
Publications (0)
Data not yet available
No reference posted for this study.