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NCT05252078RecruitingPhase 2

Anlotinib Hydrochloride Capsules Combined With TQB2450 Injection in Esophageal Squamous Cell Carcinoma Patients

An Open, Single Arm, Multicenter, Exploratory Phase II Clinical Trial of Anlotinib Hydrochloride Capsules Combined With TQB2450 Injection in Esophageal Squamous Cell Carcinoma Patients as Postoperative Adjuvant Therapy

Source: ClinicalTrials.gov · Last updated 16 Dec 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is an Open, Single Arm, Exploratory and Phase II Clinical Trial of Anlotinib Hydrochloride Capsules Combined With TQB2450 Injection in Esophageal Squamous Cell Carcinoma (ESCC) Patients as Postoperative Adjuvant Therapy. In order to observe and evaluate the efficacy and safety of Anlotinib Hydrochloride Capsules combined with TQB2450 Injection in treatment of patients with ESCC. The primary endpoint is disease free survival (DFS).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
First submitted
22 Jan 2022
Start date
2 Jun 2022
Primary completion date
Nov 2026
Lead sponsor
Jiangxi Provincial Cancer Hospital
NCT number
NCT05252078

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 30
  • From 2 Jun 2022 to the primary completion date, Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients received other antitumor adjuvant therapy after surgical resection.
  • Concurrent malignancy (except cured basal cell carcinoma of the skin).
  • Patients who have received prior targeted therapy (anti-VEGF/VEGFR) or immunity therapy (anti-PD-1/PD-L1/CTLA-4).
  • 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.
  • 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.
  • Vaccination with prophylactic or attenuated vaccine within 4 weeks prior to initial administration.

Other illness

  • Patients who are allergic to other monoclonal antibodies.
  • Patients with a history of immunodeficiency (or active autoimmue disease), or other acquired congenital immunodeficiency diseases.
  • Patients with hypertension who could not be well controlled by antihypertensive drugs (systolic blood pressure \> 160 mmHg, diastolic blood pressure \> 100 mmHg).
  • Active or uncontrolled severe infection (≥ CTC AE Grade 2 infection).
  • HIV test positive.

Lab values

  • 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.

Other

  • Patients was diagnosed cervical esophageal carcinoma.
  • Patients with multiple factors affecting oral administration.
  • Uncontrolled pleural effusion, pericardial effusion or ascites that requires repeated drainage.
  • Proteinuria =/\>2+ and confirmed 24-hour urinary protein quantification \> 1.0 g.
  • According to the investigators' judgment, there are factors that endanger patient or prevent patients from completing the study.

Who the study is looking for

  • Subjects volunteered to join the study, signed informed consent, good compliance, with follow-up.
  • ≥ 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%.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Jiangxi Cancer Hospital
Coordinator of this site? Confirm its status
NanchangChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.