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NCT Number: NCT07665372

Liver Transplantation From Donors With HIV: Impact on Opportunistic Infections, Cancer, and Long-Term Outcomes (Expanding HOPE Liver)

This research is being done to better understand opportunistic infections and cancer in transplant recipients with HIV who receive livers from a donor with HIV compared to livers from donors without HIV.

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Key information

Conditions

HIV

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic, Arizona, Phoenix, Arizona, United States

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About this study

Previously, people with HIV in need of a transplant could only receive organs from a donor without HIV. However, in November 2013, the HIV Organ Policy Equity (HOPE) Act made it possible for people with HIV to receive organs from donors with HIV as a part of a research study.

Over the last two decades, people with HIV have received organs from donors without HIV, and in general, these recipients have done well after transplant and still maintained control of HIV. Over the last several years, people with HIV have received organs from donors with HIV, and in general, these recipients have also done well after transplant and still maintained control of HIV. Although organ transplant into people with HIV using donors with and without HIV has been successful, the use of organs from donors with HIV may increase the risk of certain opportunistic infections and cancer in some people. Opportunistic infections are when pathogens (germs) cause infections in people with weakened immune systems that would not happen, or would be mild, in people with healthy immune systems. This study will look to better understand opportunistic infections and cancer in transplant recipients with HIV (HIV R+) who receive livers from donors with HIV (HIVD+) or without HIV (HIV D-).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant meets local criteria for liver or simultaneous liver kidney (SLK) transplant.
  • Participant or legally authorized representative (in accordance with Johns Hopkins Medicine Institutional Review Board (IRB) and local IRB policy) is able to understand and provide informed consent.
  • Participant has documented HIV infection by any licensed assay or documented history of detectable HIV-1 RNA.
  • Participant is ≥ 18 years old.
  • Most recent HIV-1 RNA < 50 copies RNA/mL. Viral blips between 50-400 copies will be allowed as long as there are not consecutive measurements > 200 copies/mL. Organ recipients who are unable to tolerate Antiretroviral Therapy (ART) due to organ failure or recently started ART may be eligible despite a detectable viral load if safe and effective ART to be used by the recipient after transplantation is described.

Exclusion criteria

  • Participant has prior progressive multifocal leukoencephalopathy (PML), cryptosporidiosis of > 1 month duration, or prior primary Central Nervous System (CNS) lymphoma.
  • Participant is pregnant or breastfeeding.
  • Past or current medical problems or findings from medical history, physical examination, or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.

Treatment and study plan

HIV D+/R+

Other

Receipt of liver transplant from a deceased donor with HIV

HIV D-/R+

Other

Receipt of liver transplant from a deceased donor without HIV

Primary outcomes

  1. Incidence of a composite event of opportunistic infection or cancer in HIV D+/R+ compared to HIV D-/R+ LT

    Time frame: From transplant through end of follow up (at least 6 months year, up to 4 years post-transplant)

    Cumulative incidence of composite event of opportunistic infection or cancer

Secondary outcomes

  1. Participant survival

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Time to event (death)

  2. Graft survival

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Time to event (graft loss)

  3. Incidence of bacterial, fungal, viral, and other opportunistic infections post-transplant

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Cumulative incidence of infections

  4. Incidence and type of post-transplant cancer as determined by local pathology

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Cumulative incidence of cancer determined by local pathology

  5. Serious adverse events post-transplant

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Cumulative incidence of serious adverse events

  6. Incidence of rejection events post-transplant

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Cumulative incidence of rejection events

  7. Graft function over time measured by fibrosis-4 index and Aspartate Aminotransferase (AST) to Platelet Ratio Index

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Mean value of graft function

  8. Incidence of HIV-breakthrough and HIV persistent viral failure post-transplant

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Cumulative incidence of HIV-breakthrough and HIV persistent viral failure

  9. Incidence of new antiretroviral drug resistance and/or X4 tropic virus post-transplant

    Time frame: From transplant through end of follow up (at least 6 months, up to 4 years post-transplant)

    Cumulative incidence of new resistance and/or X4 tropic virus based on local testing

  10. Incidence of surgical and vascular transplant complications during the first year post-transplant

    Time frame: From transplant through end of follow up (at least 6 months year, up to 4 years post-transplant)

    Cumulative incidence of complications

Study contacts

Contact information is provided by the study sponsor or research team.

Christine Durand, MD

CONTACT

[email protected]

410-614-6702

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • National Institute of Allergy and Infectious Diseases (NIAID)

Registry information

Official study title

HOPE in Action Liver Transplantation From Donors With HIV: Impact on Opportunistic Infections, Cancer, and Long-Term Outcomes

Important dates

Study start
2026
Primary completion
2030
Study completion
2031
First posted
Jun 24, 2026
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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