drugset / Trial / NCT04567810

Safety, Tolerability, and Pharmacokinetics of Anti-Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Chicken Egg Antibody (IgY) (COVID-19)

NCT04567810 ↗

Phase 1 Completed 48 enrolled Stanford University
RandomizedSequentialDouble-blindPrevention

Summary

The primary objective of Part 1 (Single Ascending Dose) is to assess the safety and tolerability of anti-SARS-CoV-2 IgY when given as single-ascending doses administered intranasally to healthy participants. The primary objective of Part 2 (Multiple Dose) is to assess the safety and tolerability of anti-SARS-CoV-2 IgY when given as multiple doses administered intranasally to healthy participants. A secondary objective is to assess the pharmacokinetics of anti-SARS-CoV-2 IgY when given as multiple doses administered intranasally to healthy participants. Safety will be evaluated using adverse event (AE), physical examination (including vital signs), electrocardiogram, and clinical laboratory data. Pharmacokinetics will be evaluated by serum anti-SARS-CoV-2 IgY concentration.

Timeline

Start
2020-09-18
Primary completion
2020-12-14
Completion
2020-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject anti-SARS-CoV-2 IgY Protein / enzyme biologic 2 mg Intranasal
Subject anti-SARS-CoV-2 IgY Protein / enzyme biologic 4 mg Intranasal
Subject anti-SARS-CoV-2 IgY Protein / enzyme biologic 8 mg Intranasal

Indications