RecruitingPhase 1NCT07205926

First in Human Dose Escalation Study Evaluating the Safety and Immunogenicity of IVT's Shigella-04 Vaccine in Healthy Young Adults

First-in-human, Randomized, Double-blind, Placebo-controlled, Dose-escalation Study Evaluating the Safety and Immunogenicity of IVT Shigella-04 in Healthy Young Adults


Sponsor

Inventprise Inc.

Enrollment

60 participants

Start Date

Oct 9, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Phase 1 trial to evaluate the Safety and Immunogenicity of Inventprise's (IVT) Shigella-04 in Healthy Young Adults


Eligibility

Min Age: 18 YearsMax Age: 49 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a biological treatment called IVT Shigella-04 and a biological treatment called Placebo (0.9% saline) for people with diarrhea and shigella. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 49 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALIVT Shigella-04

Preventative vaccine for Shigella protection against 4 unique serotypes

BIOLOGICALPlacebo (0.9% saline)

Subjects dosed with 0.9% saline


Locations(1)

Medpace Clinical Pharmacology Unit

Cincinnati, Ohio, United States

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NCT07205926


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