Transgender Women Needed for a Truvada Dosing Study

Transgender women needed for a research study that involves taking daily observed doses of the HIV drug Truvada, along with Lupron injections and oral estrogen. This research involves multiple study visits, including 5 separate day-long visits for blood and colon tissue sampling.

Basic Study Requirements:

• Over 18 years of age
• HIV negative
• Transgender women not currently on hormones or willing to temporarily stop hormone therapy
• Willing to come in for 5 day-long visits at the Johns Hopkins Hospital
• Willing to come to Johns Hopkins for daily observed Truvada dosing

Earn up to $3,650.
If interested, call 443-287-7156.
Principal Investigator: Mark Marzinke, Ph.D.
Protocol Number: IRB00203162
Approved February 26, 2019. 

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Transgender patients taking or planning to begin estrogen or testosterone therapy needed for a research study of the hormone influence in skin aging.   The study involves completion of a questionnaire, de-identified photographs of the face, and donation of small tissue samples (skin biopsies, skin swabs).  This research involves a single study visit for patients who are already on hormone therapy and two study visits for patients planning to begin hormone therapy.

Basic Study Requirements:

• Over 18 years of age
• Currently on hormone therapy or planning to begin hormone therapy
• Willing to come in for one 30-minute visit at the Johns Hopkins Hospital Outpatient Center (two 30-minute visits for patients not yet on hormone therapy)

Earn $20 per skin biopsy (up to $60 if already on hormones and $120 if not)
If interested, call 410-502-SKIN (7546) or email [email protected]
Principal Investigator: Farah Succaria, M.D
Protocol Number: IRB00260762
Approved July 9, 2021. 

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Study on Multipurpose Technology for HIV & Pregnancy Prevention (HAPPY)

The purpose of the study is to examine the values and preferences for a long-acting, multipurpose prevention medication that would prevent HIV and pregnancy in individuals with childbearing potential, irrespective of gender identity. Step 1 of the study is an in-depth interview to garner participant preferences for a novel product.

 

Basic Study Requirements:

• Transgender Diverse individuals assigned female at birth

If interested, scan QR code or call (410)-502-8320.

 

Principal Investigator: Allison Agwu, MD, SCM

Protocol Number: IRB00413361