Clinical trial · Interventional
SHR-1316 in Combination With Chemotherapy in Patients With Esophageal Squamous Cell Cancer
SHR-1316, a Novel Anti-PD-L1 Antibody, in Combination With Irinotecan Liposome and Fluorouracil in Patients With Esophageal Squamous Cell Cancer: a Phase II Study
NCT03732508CI-TRIAL-00035629unknownPhase 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)
The purpose of this study is to evaluate the progression-free survival (PFS) of Chemotherapy combined with SHR-1316 in patients with advanced esophageal squamous cell cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Advanced Esophageal Squamous Cell Cancer | Esophageal Squamous Cell Carcinoma | CURATED_BROADER | 0.78 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fluorouracil | Drug | Fluorouracil | ALIAS |
| Irinotecan liposome | Drug | — | UNRESOLVED |
| SHR-1316 | Drug | Adebrelimab | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Irinotecan liposome plus SHR1316 plus fluorouracil
- interventionNames
- Drug: Irinotecan liposome
- Drug: SHR-1316
- Drug: Fluorouracil
Primary outcomes (1)
- measure
- Duration of Progression-Free Survival (PFS)
- timeFrame
- approximately 22 months
- description
- based on response evaluation criteria in solid tumors 1.1 (RECIST 1.1)
Secondary outcomes (4)
- measure
- Disease Control Rate(DCR)
- timeFrame
- approximately 22 months
- description
- based on response evaluation criteria in solid tumors 1.1 (RECIST 1.1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically or cytologically confirmed unresectable local advanced/recurrent or metastasis esophageal squamous cell carcinoma; 2. No previous systemic anti-tumor treatment; 3. Subjects must have at least one measurable tumor lesion per RECIST 1.1; 4. ECOG: 0-1; 5. Adequate organ and bone marrow function; Exclusion Criteria: 1. Allergic to monoclonal antibodies, any SHR-1316 components,Irinotecan , Fluorouracil ; 2. Prior therapy as follow: 1. Anti-PD-1 or anti-PD-L1; 2. Any experimental drugs within 4 weeks of the first dose of study medication; 3. Received major operations or serious injuries within 4 weeks of the first dose of study medication; 4. Received last dose of anticancer therapy (including chemotherapy, radiotherapy, targeted therapy, etc.) within 4 weeks of the first dose of study medication; 3. Not recovered to ≤CTCAE 1 from adverse events (except for hair loss) due to a previously anti-tumor treatment; 4. Subjects with any active autoimmune disease or history of autoimmune disease; 5. Pregnancy or breast feeding;
References
Publications (0)
Data not yet available
No reference posted for this study.