Anlotinib Hydrochloride Capsules Combined With TQB2450 Injection in Esophageal Squamous Cell Carcinoma Patients
NCT ID: NCT05252078
Last Updated: 2022-12-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE2
30 participants
INTERVENTIONAL
2022-06-02
2026-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Anlotinib
Patients in the study group will receive the following treatment:
21 days as a treatment cycle, Anlotinib 12 mg/day, Orally (D1-D14); TQB 2450 1200 mg, iv (D1).
If anlotinib is not tolerated, the dose can be reduced to 10mg or 8mg, until un-tolerable toxicity again.
Anlotinib hydrochloride
Anlotinib Hydrochloride is a capsule in the form of 8 mg ,10 mg and 12 mg, orally, once daily, 2 weeks on/1 week off.
TQB2450
TQB2450 is an injection in the form of 600 mg; 1200 mg, iv, D1.
Interventions
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Anlotinib hydrochloride
Anlotinib Hydrochloride is a capsule in the form of 8 mg ,10 mg and 12 mg, orally, once daily, 2 weeks on/1 week off.
TQB2450
TQB2450 is an injection in the form of 600 mg; 1200 mg, iv, D1.
Eligibility Criteria
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Inclusion Criteria
* ≥ 18 years old.
* ECOG performance status of 0-1
* Patients with esophageal squamous cell carcinoma pathologically diagnosed as T1-2N1-3M0 or T3-4NanyM0.
* Patients received radical (R0) resection of squamous cell carcinoma with no recurrence in imaging examination within 6-12 weeks after surgery, and need adjuvant therapy assessed by the researchers.
* Laboratory tests must be met:
* Neutrophils count =/\> 1.5 x 109/L, platelets count =/\> 75 x 109/L, Hb =/\> 90 g/L, WBC =/\> 3 x 109/L.
* total bilirubin =/\< 1.5 x ULN, ALT and AST =/\< 2.5 x ULN.
* Creatinine =/\< 1.5 x ULN.
* APTT, INR, PT =/\< 1.5 x ULN.
* TSH =/\< ULN.
* Myocardial enzymes in the normal range.
* LVEF =/\> 50%.
Exclusion Criteria
* Concurrent malignancy (except cured basal cell carcinoma of the skin).
* Patients was diagnosed cervical esophageal carcinoma.
* Patients who have received prior targeted therapy (anti-VEGF/VEGFR) or immunity therapy (anti-PD-1/PD-L1/CTLA-4).
* Patients who are allergic to other monoclonal antibodies.
* Patients with a history of immunodeficiency (or active autoimmue disease), or other acquired congenital immunodeficiency diseases.
* Immunosuppressant, systemic, or absorbable local hormone therapy (\> 10mg/ day of prednisone or other equivalent hormone) is required for immunosuppression and continued within 2 weeks of initial administration.
* Patients with multiple factors affecting oral administration.
* Uncontrolled pleural effusion, pericardial effusion or ascites that requires repeated drainage.
* With bleeding tendency. Patients with any bleeding or bleeding event CTC AE grade 3 in the 4 weeks prior to initial administration. The presence of digestive diseases or active bleeding of unresected tumors, or other conditions that the investigator determined which could lead to gastrointestinal bleeding or perforation.
* Active or untreated CNS metastases as determined by CT or magnetic resonance imaging (MRI) evaluation during screening and prior radiographic assessments.
* Patients with hypertension who could not be well controlled by antihypertensive drugs (systolic blood pressure \> 160 mmHg, diastolic blood pressure \> 100 mmHg).
* Patients with myocardial infarction, myocardial ischemia, arrhythmias with poor control (including QTC interval male \> 450 ms, female\> 470 ms) and cardiac insufficiency of grade II according to NYHA standard.
* Active or uncontrolled severe infection (≥ CTC AE Grade 2 infection).
* HIV test positive.
* Proteinuria =/\>2+ and confirmed 24-hour urinary protein quantification \> 1.0 g.
* Vaccination with prophylactic or attenuated vaccine within 4 weeks prior to initial administration.
* According to the investigators' judgment, there are factors that endanger patient or prevent patients from completing the study.
18 Years
ALL
No
Sponsors
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Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
INDUSTRY
Jiangxi Provincial Cancer Hospital
OTHER
Responsible Party
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Principal Investigators
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Changying Guo, PhD
Role: PRINCIPAL_INVESTIGATOR
Jiangxi Provincial Cancer Hospital
Locations
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Jiangxi Cancer Hospital
Nanchang, Jiangxi, China
Countries
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Central Contacts
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Facility Contacts
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Changying Guo
Role: primary
Other Identifiers
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2021ky222
Identifier Type: -
Identifier Source: org_study_id