drugset / Trial / NCT06879067

Safety, Tolerability and Immune Effects of the Nasal Foralumab in Healthy Human Volunteers

NCT06879067

Phase 1 Completed 27 enrolled Tiziana Life Sciences LTD
RandomizedSequentialTriple-blindOther

Summary

The goal is to establish the safety of administration of nasal foralumab to healthy volunteers in escalating doses to determine the dose at which immune effects are observed. Patients will receive doses for 5 consecutive days and have a follow-up period.

Timeline

Start
2018-11-12
Primary completion
2019-07-23
Completion
2020-11-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Foralumab Monoclonal antibody 10 ug Intranasal
Subject Foralumab Monoclonal antibody 50 ug Intranasal
Subject Foralumab Monoclonal antibody 250 ug Intranasal

Indications

No indication recorded.