Clinical trial · Interventional
A Clinical Study of SHR-A1811 in the Treatment of HER2-positive Locally Advanced or Metastatic Biliary Tract Cancer
An Open, Multicenter Phase II Clinical Study of SHR-A1811 in the Treatment of HER2-positive Locally Advanced or Metastatic Biliary Tract Cancer
NCT06778031CI-TRIAL-00086834recruitingPhase 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 an open, multicenter Phase II clinical trial to evaluate the efficacy and safety of the SHR-A1811 combination in HER2 positive patients with locally advanced or metastatic biliary tract 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 |
|---|---|---|---|
| HER2-positive Locally Advanced or Metastatic Biliary Tract Cancer | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SHR-1316 | Drug | Adebrelimab | ALIAS |
| SHR-8068 | Drug | — | UNRESOLVED |
| SHR-A1811 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- The SHR-A1811 combination group
- interventionNames
- Drug: SHR-A1811
- Drug: SHR-1316
- Drug: SHR-8068
Primary outcomes (1)
- measure
- Objective response rate (ORR) of the SHR-A1811 combination evaluated by investigators
- timeFrame
- Screening up to study completion, an average of 3 year.
Secondary outcomes (5)
- measure
- Duration of response (DoR) of the SHR-A1811 combination evaluated by investigators
- timeFrame
- Screening up to study completion, an average of 3 year.
- measure
- Disease control rate (DCR) of the SHR-A1811 combination evaluated by investigators
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age 18-75 years old (including both ends), male or female; 2. ECOG-PS score: 0 or 1; 3. Expected survival ≥ 12 weeks; 4. Locally advanced or metastatic biliary tract cancer confirmed by histopathology or cytology; 5. Subjects who had not previously received any systemic antitumor therapy were allowed to have previously received radical therapy, and had received the last dose of radical therapy for at least 6 months until disease recurrence; 6. According to the RECIST v1.1 standard, the subjects had at least one measurable lesion; 7. The main organ function is normal, in line with the program requirements; 8. Consent to contraception. Exclusion Criteria: 1. Other active malignancies within 5 years or at the same time; 2. Local antitumor therapy was received within 4 weeks prior to initiation of treatment; 3. Subjects with biliary obstruction should be excluded; 4. There is active autoimmune disease or a history of autoimmune disease that may recur; 5. Known or suspected history of interstitial pneumonia or interstitial lung disease, or prior history of interstitial pneumonia or interstitial lung disease requiring hormone therapy; 6. Severe infection within 4 weeks prior to initiation of study treatment; 7. Active hepatitis B virus (HBV) infection; 8. Have serious cardiovascular and cerebrovascular diseases.
References
Publications (0)
Data not yet available
No reference posted for this study.