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临床试验/CTIS2023-509576-42-00
CTIS2023-509576-42-00进行中(未招募)1 期

A Phase III, Double-blind, Placebo controlled, Multi-center International Study of Neoadjuvant/Adjuvant Durvalumab for the Treatment of Patients with Resectable Stages II and III Non-small Cell Lung Cancer (AEGEAN). - D9106C00001

AstraZeneca AB0 个研究点目标入组 751 人开始时间: 2024年6月24日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
751

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Age =18 years., A pre- or post-bronchodilator FEV of 1.0 L and >40% post-operative predicted value., Newly diagnosed and previously untreated patients with histologically or cytologically documented NSCLC with resectable (Stage IIA to select [ie, N2] Stage IIIB) disease., World Health Organization (WHO)/ECOG PS of 0 or 1 at enrollment., At least 1 lesion, not previously irradiated, that qualifies as a RECIST 1.1 Target Lesion (TL) at baseline., No prior exposure to immune-mediated therapy including, but not limited to, other anti-CTLA-4, anti-PD-1, anti-PD-L1, and anti-PD-L2 antibodies, excluding therapeutic anticancer vaccines., Adequate organ and marrow function., Confirmation of a patient's tumour PD-L1 status., Provision of sufficient tumour biopsy sample for evaluation and confirmation of EGFR and ALK status., Planned surgery to be performed need to include lobectomy, sleeve resection or bilobectomy.

排除标准

  • History of allogeneic organ transplantation., Known allergy or hypersensitivity to any of the study drugs or excipients., Existence of more than one primary tumour such as mixed small cell and NSCLC histology., Patients who are candidates to undergo only pneumonectomy, segmentectomies or wedge resections., Patients with a documented test result confirming the presence of EGFRm or ALK translocation., Active or prior documented autoimmune or inflammatory disorders (including inflammatory bowel disease, diverticulitis, systemic lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome)., History of another primary malignancy., History of active primary immunodeficiency., Active infection including tuberculosis hepatitis B and C, or human immunodeficiency virus., Deemed unresectable NSCLC by multidisciplinary evaluation., Patients who have preoperative radiotherapy treatment as part of their care plan., Patients who have brain metastases or spinal cord compression., Stage IIIB N3 and Stages IIIC, IVA, and IVB NSCLC.

研究者

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