跳至主要内容
临床试验/CTIS2023-504150-35-00
CTIS2023-504150-35-00招募中1 期

Akynzeo as antiemetic treatment in patients with endometrial cancer treated with taxane - platinum combination chemotherapy. NOEME study.

Fondazione IRCCS Istituto Nazionale Dei Tumori0 个研究点目标入组 84 人开始时间: 2023年7月19日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
84

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+(—)

入选标准

  • Subject is at least 18 years of age, able to understand the study procedures, and agrees to participate in the study by providing written informed consent., Subject has histologically or cytologically proven endometrial cancer., Patients were required to have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2., Adequate organ function allowing the patient to receive taxane-platinum combination therapy with or without immunotherapy according to clinical practice and opinion of treating physician., Naive to chemotherapy.

排除标准

  • Patients will experience emesis within the 24 hours before receipt of 1 course of chemotherapy., Patients will be scheduled to radiation therapy to the abdomen or pelvis within 1 week before day 1 or between day 1 and 5., Patients will be scheduled to undergo bone marrow or stem-cell transplant., Chronic systemic corticosteroid use., Brain metastasis., Subject is considered a poor medical risk due to a serious, uncontrolled medical disorder., History or predisposition to cardiac conduction abnormalities, torsade des pointes or severe cardiovascular diseases., Subject is pregnant or breastfeeding or is expecting to conceive children within the projected duration of the study, starting with the screening visit through 180 days after the last dose of study treatment.

研究者

相似试验