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临床试验/CTIS2022-502139-20-00
CTIS2022-502139-20-00进行中(未招募)1 期

Semaglutide Treatment for Prevention of Toxicity in High-dose Chemotherapy with Autologous Hematopoietic Stem Cell Transplantation – a randomized, double-blind, placebo-controlled, investigator-initiated study - PROTECT

Rigshospitalet0 个研究点目标入组 40 人开始时间: 2022年11月22日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
40

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

  • Referral for auto-HSCT for relapsed diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma, Age = 18 years, BMI = 18.5, ECOG performance status = 2, Literate in Danish and/or English

排除标准

  • Diabetes, Pregnant or nursing females, Previous or current gastrointestinal malignancy, Personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2. Family is defined as a first degree relative, Genetic disorders with defective tissue repair (e.g. Fanconi anaemia), History of pancreatitis (acute or chronic), Renal impairment measured as estimated Glomerular Filtration Rate (eGFR) value of < 30 ml/min/1.73 m2 as defined by KDIGO 2012 classification4, Impaired liver function, defined as ALT = 2.5 times upper normal limit at screening, Known or suspected hypersensitivity to semaglutide or other GLP-1RA, Inflammatory bowel disease

研究者

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