A Phase 3 Trial to Evaluate the Long-Term Safety and Efficacy of Navenibart in Participants with Hereditary Angioedema (ORBIT-EXPANSE)

未提供0 个研究点目标入组 11 人开始时间: 待定

适应症

试验速览

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•Participants from STAR-0215-301 who met one of the following conditions:
•a. Completed STAR-0215-301 through the Day 181 visit
•b. Withdrew from STAR-0215-301 but met the following criteria:
•i. Received 2 doses of IP ii. completed >= 2 months of trial follow-up after the second dose of IP iii. Met other eligibility criteria as assessed by Investigator

•Participation in an investigational clinical trial other than STAR-0215- 301 in the 30 days or any exposure to an investigational drug (other than navenibart in STAR-0215-301) within 5 half-lives before informed consent/assent
•Any exposure to angiotensin-converting enzyme (ACE) inhibitors or any estrogen containing medications with systemic absorption (such as hormonal contraceptives or hormone replacement therapy) within 30 days before Screening.
•Known sensitivity to the ingredients in the formulation of IP

发起方

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