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NCT04310943CompletedPhase 2

Efficacy and Safety of Tislelizumab Combined With Bevacizumab and Albumin Paclitaxel in Lung Adenocarcinoma

Tislelizumab Combined With Bevacizumab and Albumin Paclitaxel in the Treatment of Advanced Lung Adenocarcinoma: a Single-arm, Phase Ⅱ Clinical Trial

Source: ClinicalTrials.gov · Last updated 6 Mar 2024

Brief summary (registry, in English)

The single arm clinical study is to evaluate the efficacy and safety of Tislelizumab combined with Bevacizumab and albumin paclitaxel in the treatment of advanced lung adenocarcinoma. All of the patients were received EGFR-TKI therapy for 1 line and disease progression. The primary endpoint is six months PFS and safety, the seconday endpoint is ORR and one-year OS rate.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
24 (actual)
First submitted
13 Mar 2020
Start date
1 Mar 2021
Primary completion date
1 Jun 2023
Lead sponsor
Zhou Chengzhi
Diseases
Lung cancer
NCT number
NCT04310943

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 24
  • From 1 Mar 2021 to the primary completion date, 1 Jun 2023
  • 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

  • have received checkpoint inhibitor.
  • patients who were treated with systemic glucocorticoids (\>10mg/ day prednisone therapeutic dose) or other immunosuppressive drugs within 14 days prior to the initial administration or during the study period

Other illness

  • any unstable systemic disease

Other

  • histology of mixed NSCLC with squamous cell carcinoma, neuroendocrine carcinoma and small cell carcinoma.
  • uncontrolled pleural effusion, pericardial effusion, or ascites after appropriate intervention

Who the study is looking for

  • lung adenocarcinoma stage Ⅳ(according AJCC 8)
  • received EGFR-TKI for 1 line and disease progression
  • EGFR T790M negative
  • ECOG PS 0-2

Age in the registry: 18 years to 75 years · 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
Zhou Chengzhi
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

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