drugset / Trial / NCT05751642

Safety and Tolerability, Pharmacokinetic, and Pharmacodynamic Study of ALXN1920 in Healthy Participants

NCT05751642 ↗

Phase 1 Completed 48 enrolled Alexion Pharmaceuticals, Inc.
RandomizedSequentialTriple-blindBasic science

Summary

This study will assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of single ascending doses (SADs) of ALXN1920 subcutaneous (SC) and of a single dose of ALXN1920 intravenous (IV) in healthy adult participants.

Timeline

Start
2023-04-19
Primary completion
2023-12-04
Completion
2023-12-04

Drugs

EvaluationDrugModalityDoseRoute
Subject ALXN1920 Unknown — Subcutaneous

Indications

No indication recorded.