Condition: Vaccine · Crimean-Congo Hemorrhagic Fever · Sponsor: HDT Bio
The goal of this clinical trial is to assess the safety, tolerability and immunogenicity of three dosage levels, and a single or two-dose administration regimen, of the investigational HDT-321 product administered intra-muscularly. The main questions it aims to answer are: * Is HDT-321 safe to use * Does HDT-321 provide protection against Crimean-Congo hemorrhagic fever virus (CCHFV) Researchers will record any adverse events and test blood samples to see if HDT-321 is safe and works to protect participants against Crimean-Congo hemorrhagic fever virus (CCHFV) Participants will: * Receive 1 or 2 doses of HDT-321 * Complete a memory aid and measurements for 7 days after receiving each dose of HDT-321 * Be followed throughout the study using phone calls and clinic visits to check for and record adverse events * Provide blood samples at specific study visits
This description comes directly from the study's public registry record.
James Keary · 206-567-8230 · james.keary@hdt.bio
Aude Frevol · 206-704-5705 · aude.frevol@hdt.bio
Always discuss trial participation with your own doctor first.
| Flourish Research San Antonio (Clinical Trials of Texas) | San Antonio, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06799013