NL-OMON26386招募中不适用
A prospective single-centre study on the efficacy and safety of 4 weekly pasireotide LAR administration in combination with or without weekly pegvisomant in previously controlled acromegaly subjects with combined treatment of long-acting somatostatin analogues and weekly pegvisomant.
Erasmus University Medical Center Rotterdam0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 60
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
入选标准
- •Written informed consent male or female aged ≥ 18 years
- •- Documentation supporting the diagnosis of acromegaly based on elevated GH and/or IGF-I levels due to a pituitary tumor
排除标准
- •- Has undergone pituitary surgery or radiotherapy within 6 months prior to study entry.
研究者
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