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Clinical Trials in China / NCT06778031
Recruiting Phase 2

A Clinical Study of SHR-A1811 in the Treatment of HER2-positive Locally Advanced or Metastatic Biliary Tract Cancer

NCT06778031 · tracked via the Priya Life Science China tracker
Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Phase
Phase 2
Started
2025-02-26
Last updated
2025-03-06

Condition(s) studied

HER2-positive Locally Advanced or Metastatic Biliary Tract Cancer

Investigational drug(s) / intervention(s)

SHR-A1811 →SHR-1316 →SHR-8068 →

SHR-A1811: SHR-A1811.

SHR-1316: SHR-1316.

SHR-8068: SHR-8068.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Affiliated Cancer Hospital of Harbin Medical University Harbin Heilongjiang Recruiting
Zhongshan Hospital, Fudan University Shanghai Shanghai Municipality Recruiting

More Suzhou Suncadia Biopharmaceuticals Co., Ltd. trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06778031 on ClinicalTrials.gov ↗ ← All trials in China