跳至主要内容
临床试验/CTIS2023-507385-11-00
CTIS2023-507385-11-00招募中1 期

ong-Term Follow-Up of Subjects Treated With NTLA-2001 - ITL-2001-CL-999

Intellia Therapeutics Inc.0 个研究点目标入组 72 人开始时间: 2024年4月8日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
72

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

  • 1. A participant has completed or discontinued from an Intellia-sponsored clinical study in which a complete or partial dose of NTLA-2001 was received., 2. A participant has provided informed consent for the LTFU study., 3. A participant is willing to attend study visits, complete protocol-required follow-up schedule, and comply with the study requirements.

排除标准

  • 未提供

研究者

发起方
Intellia Therapeutics Inc.

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