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IBI310 in Combination With Sintilimab in Patients With Advanced Biliary Tract Cancer

Primary Purpose

Advanced Biliary Tract Cancer

Status
Recruiting
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
IBI310
sintilimab
Sponsored by
Innovent Biologics (Suzhou) Co. Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Advanced Biliary Tract Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: The subject must sign the written informed consent form, and can comply with the visits and related procedures specified in the protocol. Aged ≥18 years. Patients with unresectable or relapsed or metastatic advanced Biliary tract cancer,and diagnosed by histology/cytology (except carcinoma of ampulla). Had progressed after receiving at least first-line systemic treatment (if a patient has progressed within 6 months after receiving systemic treatment during adjuvant chemotherapy or concurrent radiochemotherapy, she will be deemed to have received first-line treatment). Patients who have never received any anti-PD-1, anti-PD-L1/L2 antibody, anti-CTLA-4 antibody, or other immunotherapy. The subject must have at least one measurable lesion as the target lesion (according to RECIST V1.1). A measurable lesion in the radiation field from previous radiotherapy or local treatment, can also be chosen as the target lesion if confirmed progression. Exclusion Criteria: Diagnosis of other malignant tumors within 5 years before the first administration, excluding radically cured skin basal cell carcinoma, skin squamous cell carcinoma, radically resected carcinoma in situ and/or thyroid papillary carcinoma. Patients who have previously received organ or bone marrow transplantation. Patients with acute or chronic active hepatitis B or C infection, hepatitis B virus (HBV) DNA> 2000 IU/ml or 104 copies/ml; hepatitis C virus (HCV) antibody positive and HCV-RNA >103 copies/ml;. Patients with acute or chronic active hepatitis B or C infection who have received nucleotide antiviral therapy and are below the above standards can be selected. Uncontrollable hypertension, systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥100 mmHg after best medical treatment, history of hypertensive crisis or hypertensive encephalopathy. Pleural effusion, ascites, and pericardial effusion with clinical symptoms or requiring drainage , patients who only shows with a few pleural effusion, ascites, and pericardial effusion by imaging and with no clinical symptoms can be selected.

Sites / Locations

  • Hunan cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

IBI310+ sintilimab

Arm Description

All Subjects will be treated with : Sintilimab 200mg IV Q3W continuously and IBI310 2mg/kg IV single dose, 3 weeks later, IBI310 maintenance dose is 1mg/kg IV Q6W until progression (treatment duration up to 24 months).

Outcomes

Primary Outcome Measures

Objective response rate (ORR)
Investigator evaluated ORR per RECIST V1.1

Secondary Outcome Measures

progression free survival, PFS
PFS is defined as the time from first treatment to the date of the first documented tumor progression as determined by the investigator (per RECIST 1.1), or death due to any cause.
duration of response, DoR
Defined as the time from the first documented objective response to the first documented progressive disease or death of any cause, whichever occurs first;
disease control rate, DCR
Defined as the proportion of patients whose best response is CR, PR, and stable disease (SD) non-CR/non-PD
Overall Survival,OS
OS is defined as the time from enrollment to the date of death.

Full Information

First Posted
December 6, 2022
Last Updated
March 31, 2023
Sponsor
Innovent Biologics (Suzhou) Co. Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT05653180
Brief Title
IBI310 in Combination With Sintilimab in Patients With Advanced Biliary Tract Cancer
Official Title
A Single Arm,Multi-center,Phase Ib/II Clinical Study Evaluating IBI310 Combined With Sintilimab in Patients With Advanced Biliary Tract Cance(BTC)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 10, 2023 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
June 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Innovent Biologics (Suzhou) Co. Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This research study is designed to establish whether the combination of IBI310 & Sintilimab has efficacy in patients with advanced BTC

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Biliary Tract Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IBI310+ sintilimab
Arm Type
Experimental
Arm Description
All Subjects will be treated with : Sintilimab 200mg IV Q3W continuously and IBI310 2mg/kg IV single dose, 3 weeks later, IBI310 maintenance dose is 1mg/kg IV Q6W until progression (treatment duration up to 24 months).
Intervention Type
Drug
Intervention Name(s)
IBI310
Intervention Description
2mg/kg IV,3 weeks later, 1mg/kg IV Q6W
Intervention Type
Drug
Intervention Name(s)
sintilimab
Other Intervention Name(s)
IBI308
Intervention Description
200mg IV Q3W
Primary Outcome Measure Information:
Title
Objective response rate (ORR)
Description
Investigator evaluated ORR per RECIST V1.1
Time Frame
up to 24 months
Secondary Outcome Measure Information:
Title
progression free survival, PFS
Description
PFS is defined as the time from first treatment to the date of the first documented tumor progression as determined by the investigator (per RECIST 1.1), or death due to any cause.
Time Frame
up to 24 months
Title
duration of response, DoR
Description
Defined as the time from the first documented objective response to the first documented progressive disease or death of any cause, whichever occurs first;
Time Frame
up to 24 months
Title
disease control rate, DCR
Description
Defined as the proportion of patients whose best response is CR, PR, and stable disease (SD) non-CR/non-PD
Time Frame
up to 24 months
Title
Overall Survival,OS
Description
OS is defined as the time from enrollment to the date of death.
Time Frame
up to 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The subject must sign the written informed consent form, and can comply with the visits and related procedures specified in the protocol. Aged ≥18 years. Patients with unresectable or relapsed or metastatic advanced Biliary tract cancer,and diagnosed by histology/cytology (except carcinoma of ampulla). Had progressed after receiving at least first-line systemic treatment (if a patient has progressed within 6 months after receiving systemic treatment during adjuvant chemotherapy or concurrent radiochemotherapy, she will be deemed to have received first-line treatment). Patients who have never received any anti-PD-1, anti-PD-L1/L2 antibody, anti-CTLA-4 antibody, or other immunotherapy. The subject must have at least one measurable lesion as the target lesion (according to RECIST V1.1). A measurable lesion in the radiation field from previous radiotherapy or local treatment, can also be chosen as the target lesion if confirmed progression. Exclusion Criteria: Diagnosis of other malignant tumors within 5 years before the first administration, excluding radically cured skin basal cell carcinoma, skin squamous cell carcinoma, radically resected carcinoma in situ and/or thyroid papillary carcinoma. Patients who have previously received organ or bone marrow transplantation. Patients with acute or chronic active hepatitis B or C infection, hepatitis B virus (HBV) DNA> 2000 IU/ml or 104 copies/ml; hepatitis C virus (HCV) antibody positive and HCV-RNA >103 copies/ml;. Patients with acute or chronic active hepatitis B or C infection who have received nucleotide antiviral therapy and are below the above standards can be selected. Uncontrollable hypertension, systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥100 mmHg after best medical treatment, history of hypertensive crisis or hypertensive encephalopathy. Pleural effusion, ascites, and pericardial effusion with clinical symptoms or requiring drainage , patients who only shows with a few pleural effusion, ascites, and pericardial effusion by imaging and with no clinical symptoms can be selected.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tengfei Zhou
Phone
+86 0512-69566088
Email
tengfei.zou@innoventbio.com
Facility Information:
Facility Name
Hunan cancer Hospital
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tao Zhang
Phone
+86 027-85726114
Email
1277577866@qq.com
First Name & Middle Initial & Last Name & Degree
Jia Luo
Phone
+86 0731-89762030
Email
luojia@hnca.org.cn

12. IPD Sharing Statement

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IBI310 in Combination With Sintilimab in Patients With Advanced Biliary Tract Cancer

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