24 Participants Needed

MGD020 + MGD014 for HIV

(DELIVER-02 Trial)

Recruiting at 2 trial locations
SP
Overseen BySusan Pedersen
Age: 18+
Sex: Any
Trial Phase: Phase 1
Sponsor: University of North Carolina, Chapel Hill
Must be taking: Antiretrovirals
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores the safety and tolerance of two experimental antibody treatments, MGD014 and MGD020, for people living with HIV. Vorinostat, a drug that helps reveal hidden HIV in cells, is also used to assess how the antibodies perform in different scenarios. Participants will be divided into three groups to test these treatments in various combinations, with one group temporarily pausing their usual HIV medications. This trial may suit individuals who have maintained stable antiretroviral therapy (ART) for at least two years and have not recently shown high levels of HIV in their blood. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive these new treatments.

Do I have to stop taking my current medications for the trial?

If you are in group B, you will need to stop taking your antiretroviral therapy (ART) for up to 8 weeks during the trial. If you are in groups A or C, you will continue your current ART.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research is investigating the safety of using MGD014 and MGD020 together in people with HIV who are also on antiretroviral therapy (ART). Early results suggest this combination might be safe, but it remains under close study. Researchers monitor the body's reactions to these drugs and any potential side effects.

For the combination of MGD014, MGD020, and Vorinostat, research is in its initial stages. As this is a Phase 1 trial, the primary goal is to assess the treatment's safety and tolerability. Scientists are examining any side effects and their severity.

Vorinostat has approval for some other conditions, providing some knowledge about its safety in humans. However, its use with MGD014 and MGD020 is new, requiring further information to confirm safety.

In a Phase 1 trial, safety is the top priority, and researchers carefully monitor all participants for any adverse effects.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about the treatments MGD014 and MGD020 for HIV because they offer a novel approach compared to current options, like antiretroviral therapy. MGD014 and MGD020 work by enhancing the immune response against HIV, potentially offering a new mechanism to control the virus. Unlike standard treatments that require daily medication, these investigational drugs are administered via infusions, which may lead to longer-lasting effects. Additionally, the combination of MGD014 and MGD020 with temporary treatment interruption or Vorinostat could provide insights into optimizing HIV management, making these treatments a promising frontier in HIV therapy.

What evidence suggests that this trial's treatments could be effective for HIV?

Research has shown that MGD014 and MGD020 are promising treatments for HIV. Early lab studies indicate that MGD014 helps certain white blood cells, called T cells, effectively kill cells infected with HIV. MGD020 targets specific parts of the HIV virus to support the immune system. In this trial, participants will receive infusions of MGD014 and MGD020. Some participants will receive these infusions alone, while others will receive them with a temporary treatment interruption or with Vorinostat. When used together, MGD014 and MGD020 have shown greater effectiveness in reducing dormant HIV in cells. In studies with humanized mice, this combination significantly improved the ability to target HIV. These findings suggest that these treatments could effectively manage HIV.12467

Who Is on the Research Team?

CL

Cynthia L. Gay, MD

Principal Investigator

University of North Carolina, Chapel Hill

Are You a Good Fit for This Trial?

This trial is for people with HIV who are on antiretroviral therapy. Participants must be willing to potentially pause their current HIV treatment and receive experimental antibodies, MGD014 and MGD020, through IV infusions. Some will also take Vorinostat orally.

Inclusion Criteria

HIV infection documented by licensed rapid HIV test, HIV antibody test, or HIV Ag/Ab assay
Confirmation of HIV infection by licensed Western blot, a second antibody test, or HIV-1 antigen, plasma HIV-1 RNA viral assay
Able and willing to give written informed consent
See 21 more

Exclusion Criteria

Recent participation in other investigational treatments
Non-HIV related immune deficiency
Allergy or hypersensitivity to study drug components
See 19 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive MGD014 and MGD020 infusions, with some groups also receiving Vorinostat or undergoing a temporary treatment interruption

6-12 weeks
13 or 18 visits, depending on group assignment

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessments of adverse events and pharmacokinetics

14 weeks

Long-term Follow-up

Participants are monitored for long-term safety and immunogenicity, including anti-drug antibody formation

26 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • MGD014
  • MGD020
  • Vorinostat
Trial Overview The DART DELIVER-02 Study tests the safety of two HIV-specific antibodies (MGD014 and MGD020) and an oral medication called Vorinostat in individuals with HIV/AIDS. The study explores how these treatments affect dormant HIV in cells and measures how long the drugs stay active in the body.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Group I: Arm C - MGD014/MGD020 Infusions with VorinostatExperimental Treatment3 Interventions
Group II: Arm B - MGD014/MGD020 Infusions with Temporary Treatment Interruption (TTI)Experimental Treatment3 Interventions
Group III: Arm A - MGD014/MGD020 InfusionsExperimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of North Carolina, Chapel Hill

Lead Sponsor

Trials
1,588
Recruited
4,364,000+

US Military HIV Research Program

Collaborator

Trials
20
Recruited
3,900+

Henry M. Jackson Foundation for the Advancement of Military Medicine

Collaborator

Trials
103
Recruited
94,300+

National Institute of Allergy and Infectious Diseases (NIAID)

Collaborator

Trials
3,361
Recruited
5,516,000+

United States Department of Defense

Collaborator

Trials
940
Recruited
339,000+

Citations

A Study of MGD020 Alone or Combined With MGD014 in ...A phase 1, open-label, dose-escalation, and multi-dose expansion study of MGD020 as a single agent or in combination with MGD014 in persons with HIV-1 (PWH) on ...
Bispecific antibody-derived molecules to target persistent ...This study will also evaluate the safety and PK of the MGD014 + MGD020 combination. The results from these studies will support future clinical studies in which ...
A Study of MGD020 Alone or Combined With MGD014 in ...Study CP-MGD020-01 is a phase 1, open-label, dose-escalation, and multi-dose expansion study of MGD020 as a single agent or in combination ...
MGD020 + MGD014 for HIV · Info for ParticipantsEarly lab studies indicate that MGD014 can effectively assist T cells in killing HIV-infected cells. Although these results are promising, they are based on lab ...
Trial | NCT05261191MGD020 is a bispecific DART® molecule that binds CD3 and gp41 subunit of HIV-1 envelope. MGD014 is a bispecific DART® molecule that binds CD3 and gp120 subunit ...
The DART DELIVER-02 Study | Clinical Research Trial ...The study will measure the impact of study treatment on non-active HIV in cells, and how long MGD014 and MGD020 stay in the body after they are ...
NCT05261191The combination of MGD020 and MGD014 has the potential to enhance the recognition of rare actively infected cells in individuals that express env glycoproteins ...
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security