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PHA1A clinical trials

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NCT ID: NCT06435936 Recruiting - PHA1A Clinical Trials

A Study to Assess the Safety of SAB-176 to Prevent the Flu, Given IM in Healthy Adults Compared With Placebo

SAB-176-103
Start date: April 22, 2024
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety and tolerability of an intramuscular injection of SAB-176 intended for use as a pre/post prophylactic for influenza. This is a Phase 1, randomized, double-blind, placebo-controlled clinical trial in which a total of 28 subjects will receive an injection of either SAB-176 or placebo (normal saline). The investigational product will be administered intramuscularly (IM) on Day 1. Four dose escalation cohorts of 7 subjects (5 active and 2 placebo) each are planned. Subjects will be randomized to receive either SAB-176 or placebo in a double-blinded manner. Progression to subsequent dose-escalating cohorts will be dependent on safety measured through Day 5 after dosing of the previous cohort. Blood specimens will be collected at prescribed intervals to examine pharmacokinetics and immunogenicity. Safety will be actively monitored during investigational product administration and for 60 days following dosing. The decision to advance to the next cohort will be based solely on the safety assessment through Day 5. All safety data will be summarized and reviewed by the PI, the Sponsor's Clinical Monitor, and the Research Monitor prior to next cohort dose-escalation.

NCT ID: NCT03931668 Recruiting - PHA1A Clinical Trials

Tolerance, PK and PD Effects Study of TPN-672 in Chinese Healthy Volunteers

Start date: April 17, 2019
Phase: Early Phase 1
Study type: Interventional

This is a single-site, randomized, double-blind, placebo-controlled, incremental phase I clinical trial to evaluate preliminarily the tolerance, pharmacokinetics and pharmacodynamic effects of TPN672 maleate in Chinese healthy volunteers after single dose administration.

NCT ID: NCT03630094 Completed - PHA1A Clinical Trials

Plasma and Intrapulmonary Concentrations Study of WCK 5222

Start date: March 31, 2017
Phase: Phase 1
Study type: Interventional

This is a Phase 1, multiple dose, open-label pharmacokinetic study in healthy adult male and female subjects.