A Phase 4 Double-Blind Study to Assess the Safety and Tolerability of Intravenous Administration of GLASSIA in Healthy Adult Volunteers
收藏DataCite Commons2025-09-09 更新2026-05-07 收录
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https://search.vivli.org/doiLanding/studies/PR00011659/isLanding
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资源简介:
The purpose of this study was to generate sufficient safety and tolerability information in support of an increase in the infusion rate of intravenous GLASSIA in the prescribing information from 0.04 to 0.2 mL/kg/min.
提供机构:
Vivli
创建时间:
2025-07-30



