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Clinical Trial Summary

The goal of this study is to assess the immune response, tolerance, and safety of the low-dose intradermal (forearm) mpox vaccine in people who are HIV+ compared to people who are HIV-, and compared to the standard-dose subcutaneous (upper arm) vaccine. The resulting data will fill knowledge gaps, inform public health practices, and address community concerns about the absence of data for low-dose intradermal mpox vaccinations in people living with HIV.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05654883
Study type Observational
Source NYU Langone Health
Contact Mark J. Mulligan, MD
Phone 877-919-2822
Email Mark.mulligan@nyulangone.org
Status Recruiting
Phase
Start date November 11, 2022
Completion date December 31, 2028

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