Bringing HIV Study Protocols to Life with Representative, High-Quality Research

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This blog is the second in a series about the future of NIAID's HIV clinical research enterprise. For more information, please visit the HIV Clinical Research Enterprise page.

The impact of clinical research is often measured by its outcomes. From trials that provide groundbreaking evidence of efficacy to those stopped early for futility, the end results of clinical trials shape practice and future research priorities. However, years of effort from scientists, study teams and study participants while a trial is underway are sometimes overshadowed by final study outcomes. In this regard, trial implementation requires clinical research sites’ operational excellence for the duration of a study. Access to relevant populations depends on the location of each clinical research site as well as investigators' and clinical care providers’ engagement with the local community and understanding of their needs and preferences. A high-functioning clinical research site anchored in the communities it works in and comprised of cohesive, well-integrated components is essential to producing high-quality outputs. 

Currently, NIAID supports four research networks as part of its HIV clinical research enterprise. The networks are made up of more than 100 clinical research sites, each with local experts, robust research infrastructure, and well-trained, cross-functional staff who maintain standardized procedures and quality controls aligned with their network.

Every seven years, NIAID engages research partners, community representatives, and other public health stakeholders in a multidisciplinary evaluation of network progress toward short- and long-term scientific goals. This process takes account of knowledge gained since the networks were last funded and identifies essential course corrections based on the latest scientific and public health evidence. Subsequent NIAID HIV research investments build on the conclusions of these discussions. This process includes examining the networks’ infrastructure model, which the Institute updates and refines to stay aligned with its scientific priorities. 

The HIV clinical trials network sites have made tremendous contributions to NIH’s scientific priorities by offering direct access to and consultation with populations most affected by HIV globally, and by delivering high-quality clinical research with strong connections to trusted community outreach platforms. Their approach to community engagement anchors clinical research sites beyond the scope of any individual study, and when possible, aligns scientific questions and study protocols based on local context. 

Since the start of the 2020 research network grant cycle, HIV clinical research sites have enrolled about 93,000 participants across 78 clinical trials in 25 countries. The networks were able to quickly pivot to support NIAID’s emerging infectious disease priority areas, including COVID-19 and mpox. Of the 93,000 participants since 2020, approximately 78,000 were enrolled into COVID-19 clinical trials sponsored by NIAID’s Division of AIDS. 

Clinical trials sites currently operate with a hub-and-spoke model, with each hub providing centralized support to their linked clinical research sites. This model leverages shared resources where possible and practical, and ensures robust oversight to promote high-quality clinical trial operations. Hubs provide infrastructure and services including laboratory, pharmacy, regulatory, data management, and training to support execution of NIAID-sponsored clinical research. 

Future networks will need to maintain core strengths of current models while expanding capacity in areas vital to further scientific progress. These include operations that inform pandemic responses and extending our reach within communities impacted by HIV, including populations historically underrepresented in clinical research. Additionally, there may be opportunities for clinical research sites and other partners to conduct implementation science research based on their capacity and access to relevant populations in the context of specific scientific questions. 

Make seamless progress on established and emerging scientific priorities

Our goals include maintaining the strength and flexibility of our current network model and infrastructure to support established scientific priorities that improve the practice of medicine, including high-impact registrational trials to identify new biomedical interventions and support changes to product labelling. The networks also must remain capable of directing operations to generate evidence on interventions for pandemic responses. 

Engage underserved populations for more representative studies 

Building on its current reach, NIAID and its partners have identified opportunities to expand or strengthen our connections to medically underserved populations affected by HIV, and to increase representation of geographic areas with limited access to current clinical trials sites. We also are seeking clinical research sites with longstanding community relationships and experience conducting randomized clinical trials that include Black gay, bisexual, and other men who have sex with men, transgender people, people who sell sex, people who use drugs, and adolescent girls and young women, as well as populations in African countries with a high HIV prevalence. 

Integrate implementation science within clinical research practice

Implementation science is the scientific study of methods and strategies that facilitate the uptake of evidence-based practice and research into regular use by practitioners and policymakers. As biomedical HIV prevention, treatment, and diagnostic options expand, our scientific questions must expand to address not only whether an intervention works, but how it can be delivered to offer health care choices that people need, want and are able to use. This expanded scientific scope calls for research sites to have a diverse reach and skill sets, including experience and capacity for conducting implementation science research and fostering and maintaining partnerships with organizations that conduct implementation science research on key topics and interventions on which implementers seek stronger evidence.

The research community plays an essential role in shaping NIAID’s scientific direction and research enterprise operations. We want to hear from you. Please share your questions and comments at NextNIAIDHIVNetworks@mail.nih.gov.

About NIAID’s HIV Clinical Trials Networks

The clinical trials networks are supported through grants from NIAID, with co-funding from and scientific partnerships with NIH’s National Institute of Mental Health, National Institute on Drug Abuse, National Institute on Aging, and other NIH institutes and centers. There are four networks—Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections, the HIV Vaccine Trials Network, the HIV Prevention Trials Network, and the International Maternal Pediatric Adolescent AIDS Clinical Trials Network.

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The Antiviral Tecovirimat is Safe but Did Not Improve Clade I Mpox Resolution in Democratic Republic of the Congo

The antiviral drug tecovirimat did not reduce the duration of mpox lesions among children and adults with clade I mpox in the Democratic Republic of the Congo (DRC), based on an initial analysis of data from a randomized, placebo-controlled trial. However, the study’s 1.7% overall mortality among enrollees, regardless of whether they received the drug or not, was much lower than the mpox mortality of 3.6% or higher reported among all cases in the DRC. This shows that better outcomes among people with mpox can be achieved when they are hospitalized and provided high-quality supportive care.

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Candidate Malaria Vaccine Provides Lasting Protection in NIH-Sponsored Trials

Two National Institutes of Health (NIH)-supported trials of an experimental malaria vaccine in healthy Malian adults found that all three tested regimens were safe. One of the trials enrolled 300 healthy women ages 18 to 38 years who anticipated becoming pregnant soon after immunization. That trial began with drug treatment to remove malaria parasites, followed by three injections spaced over a month of either saline placebo or the investigational vaccine at one of two dosages.

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Charting the Path to an HIV-Free Generation

NIAID Now |

This blog is the first in a series about the future of NIAID's HIV clinical research enterprise. For more information, please visit the HIV Clinical Research Enterprise page.

NIAID supports four research networks as part of its HIV clinical research enterprise. Every seven years, the Institute engages research partners, community representatives, and other public health stakeholders in a multidisciplinary evaluation of network progress toward short- and long-term scientific goals. This process takes account of knowledge gained since the networks were last funded and identifies essential course corrections based on the latest scientific and public health evidence. Subsequent NIAID HIV research investments build on the conclusions of these discussions.

Pregnancy, childbirth and the postnatal period are a key focus of NIAID HIV research and call for measures to support the health of people who could become pregnant as well as their infants. Biological changes and social dynamics such as gender inequality, intimate partner violence, and discrimination can increase the likelihood of HIV acquisition during all natal stages. Of note, breastfeeding/chestfeeding is emerging as the predominant mode of vertical HIV transmission. NIAID is committed to optimizing HIV treatment and prevention options for people who might become pregnant, people who are pregnant and lactating, newborns, and young children who are still nursing or are living with HIV. Our goals are to offer safe, effective, acceptable, and accessible tools that provide evidence-based HIV prevention choices throughout the period of reproductive potential; prevent vertical HIV transmission to infants; and enable infants born with HIV to experience long periods of HIV remission or complete HIV clearance. We think these goals can be reached with discovery and development studies to advance biomedical interventions, and implementation science to rapidly introduce state-of-the-art interventions where they are needed most urgently.

In the current evaluation of our clinical trials networks, NIAID and other stakeholders are assessing novel interventions to interrupt the unacceptably high rate of new pediatric HIV diagnoses that persist in high burden countries. Recent research is rapidly expanding the evidence base for treatment for children and pregnant people with HIV, as well as biomedical prevention tools for pregnant people and people of reproductive potential who stand to benefit from their use. Some key advances include: 

  • Expanded evidence to support a cascade of multiple regulatory approvals making new therapeutic agents available to the youngest children with HIV;
  • Demonstrated safety of prevention products and antiretroviral therapy (ART) throughout pregnancy, including long-acting cabotegravir for HIV pre-exposure prophylaxis (PrEP); the controlled-release vaginal ring for HIV PrEP; and integrase strand transfer inhibitor-based ART for viral suppression in people with HIV; and
  • Rigorous examination of the potential of treatment initiation within hours of birth to enable ART-free HIV remission in children in a research setting.

Together, these advances open doors to improved tools for HIV prevention and treatment and help define remaining evidence gaps and research needs.

Biomedical research to accelerate evidence responsive to pediatric and perinatal needs 

As noted above, a NIAID-sponsored clinical trial led by the International Maternal Pediatric Adolescent AIDS Clinical Trials Network (IMPAACT), called IMPAACT P1115, found that four children surpassed a year of HIV remission after pausing ART. The protocol remains active with subsequent iterations of the trial in children receiving more advanced ART regimens and novel broadly neutralizing antibody-based therapy. Further research is planned to identify biomarkers to predict the likelihood of HIV remission or rebound following ART interruption. Additional studies also are needed to better understand the mechanisms by which neonatal immunity and very early ART initiation limited the formation of latent HIV reservoirs to drive the original P1115 results.

Additional research priorities include developing early infant HIV testing assays that can promptly detect vertical HIV acquisition through breastfeeding/chestfeeding; wider examination of the safety and efficacy of presumptive ART pending an HIV diagnosis; administration of very early neonatal and pediatric formulations of the latest and future generations of long-acting ARVs for prevention and treatment and antibody-based therapy; and optimization of long-acting HIV treatment regimens to support health through periods of reproductive potential, pregnancy, and lactation.    

Implementation science to strengthen delivery 

Improving HIV prevention and care through reproductive years and intense early-life HIV intervention for infants will require an unprecedented level of reproductive health, prenatal, postnatal and pediatric HIV service integration. Several key clinical and operational questions warrant investigation through implementation science. The first is assuring availability of acceptable HIV testing modalities pre-conception, as well as universal HIV testing as part of routine obstetric care, and then supporting access to a person’s preferred PrEP method or ART based on HIV status. For infants whose birthing parent has HIV, we need evidence-based models for offering very early point-of-care infant HIV diagnosis and treatment, including presumptive ART for infants exposed to HIV in utero pending confirmatory testing. We also need to understand how to better support continued engagement in care to maintain viral suppression for childbearing people with HIV through the end of the lactating period and life course. We will provide special consideration for the preferences of adolescent and young adult cisgender women who are disproportionately affected by HIV in high burden settings globally. Defining local and contextually appropriate adaptations of successful models will be paramount for successful uptake. 

The research community plays an essential role in shaping NIAID’s scientific direction and research enterprise operations. We want to hear from you. Please share your questions and comments at NextNIAIDHIVNetworks@mail.nih.gov.

About NIAID Clinical Trials Networks and Pediatric HIV

The IMPAACT Network examines prevention and treatment interventions for HIV, HIV-associated complications, and related pathogens in infants, children, and adolescents, and during pregnancy and postpartum periods. The Network is supported through grants from NIAID, with co-funding and scientific partnership from the NIH Eunice Kennedy Shriver National Institute of Child Health and Human Development and the NIH National Institute of Mental Health. Three other networks—the HIV Vaccine Trials Network, HIV Prevention Trials Network, and Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections—generate complementary evidence and provide research infrastructure where needed when rapidly evolving prevention and treatment science has implications for IMPAACT priority populations. 

Editorial note: NIAID encourages the use of inclusive language in all communications. The terms related to lactation and pregnancy in this blog reflect the diverse gender identities and experiences of all people who stand to benefit from HIV prevention and cure research. For more information on inclusive language related to pregnancy and family, please visit the NIAID HIV Language Guide.  

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Exploratory Analysis Associates HIV Drug Abacavir with Elevated Cardiovascular Disease Risk in Large Global Trial

Current or previous use of the antiretroviral drug (ARV) abacavir was associated with an elevated risk of major adverse cardiovascular events (MACE) in people with HIV, according to an exploratory analysis from a large international clinical trial primarily funded by the National Institutes of Health (NIH). There was no elevated MACE risk for the other antiretroviral drugs included in the analysis. The findings will be presented at the 2024 International AIDS Conference (AIDS 2024) in Munich, Germany.

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NIAID's Approach to Women's Health Research

Why Is Women's Health a Priority for NIAID?

The National Institute of Allergy and Infectious Diseases (NIAID) mission is to conduct and support basic and translational research to understand, diagnose, prevent and treat infectious and immune-mediated diseases, including diseases that impact the health of women and girls. NIAID takes measures to ensure the involvement of women in clinical trials on various infectious and auto-immune diseases.

Scientific Advances in Women's Health Research

NIH Statement on Preliminary Efficacy Results of Twice-Yearly Lenacapavir for HIV Prevention in Cisgender Women

The injectable antiretroviral drug lenacapavir was safe and 100% effective as long-acting HIV pre-exposure prophylaxis (PrEP) among cisgender women in a Phase 3 clinical trial, according to top-line findings released by Gilead Sciences, Inc., the study sponsor. Lenacapavir is administered every six months, making it the most durable HIV prevention method to have shown efficacy in this population.

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Stepping into Science

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‘Stepping into Science’ Highlights Variety of Scientific Careers

NIAID’s RML Campus Hosts Day-Long High School Program

Introducing local students to biomedical science and research has long been a feature of outreach programs at NIAID’s Rocky Mountain Laboratories in Hamilton, Montana.  However, realizing that traditional laboratory science – aka “bench research” – isn’t for everyone, RML staff recently invited two dozen area high school students to experience not only traditional research but also the lesser-known careers that make bench research possible.

Where bench science can be slow and methodical – scientists may spend their entire career investigating the same problem – jobs that support bench research often vary greatly from project to project. Both types of careers are rewarding and exciting – but appeal to different types of people.

“Stepping into Science,” held this spring at the RML campus, was the idea of Kamryn Cregger, who began postbaccalaureate research work at RML in August 2023. Cregger says she quickly realized that RML had amazing resources to benefit area students, and she hoped to provide them with a similar type of opportunity that she experienced as a high schooler in rural Maryland. Cregger enrolled in a biomedical leadership program that led to a pharmaceutical internship, two years of lab training, and ultimately a bachelor’s degree in plant sciences from the University of Tennessee.

Now working on tickborne disease projects at RML – and helping local middle-school students through RML’s Biomedical Research After School Scholars program – Cregger wanted to find a way to connect with college-bound high schoolers.

“With all of the scientists and staff members on site, why not show the local students what kinds of jobs there are in science in addition to bench work?” she thought. Making those types of connections also could establish the RML group as long-term mentors for students applying for college, internships, or career positions.

After a few months of planning meetings, coordinating with RML volunteers, and finding out what most appealed to students and faculty from Hamilton and Corvallis high schools – the groups arrived for the whirlwind day of activities at RML.

“Throughout the day,” Cregger said, “students asked questions about careers, RML research, medical school application processes, the differences in academic versus government research and even vaccine development!” Students received a campus tour, overview of the types of research done in the different laboratory groups and rotated through three hands-on demonstrations by virologists, animal care staff and  microscopists.

A team of RML virologists worked together to demonstrate biosafety knowledge, proper laboratory skills, such as pipetting, working in a biosafety cabinet, and dressing in personal protective equipment (PPE). They even designed a way for students to participate in a fun research-based game.

The three microscopists – Forrest Hoyt, Sophia Antonioli-Schmit and Bryan Hansen – all discussed their remarkable journeys from local high schools to RML.

In the animal care segment, “We taught them about animal husbandry, histology technicians, biologists and veterinarians,” veterinary pathologist Carl Shaia said. “Someone in each of those positions described their duties, education and how they came to RML. We also briefly touched on pay, the importance of benefits and the impact of student debt for higher education.”

RML biologist Tara Wehrly’s daughter participated in the events. Wehrly said she appreciated how the activities gave her daughter a greater understanding of the work she does.

“My daughter knows I work here, and I talk about scientific matters, but until she was on campus, it was more of an abstract concept,” Wehrly said. “I feel that Kamryn (Cregger) found the right people to give enthusiastic, informative presentations communicating the fun parts of their jobs to this group of teenagers. The discussions the kids had with post-bacs and post-docs gave them information about potential career paths that they might not have considered prior to this.”

Cregger and other event organizers already are discussing where to take the idea next, starting off with hopes of continuing the program for years to come. RML would like to inspire generations of science-loving people “and is honored to help guide the students down whatever path they choose,” according to Cregger. 

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Apply to Develop Global Infectious Disease Research Training Programs

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A significant obstacle to advancing evidence-based treatment and control of infectious diseases in low- and middle-income countries (LMICs) is the lack of capability to conduct research tailored to local needs. As a result, NIAID, in partnership with the Fogarty International Center (FIC), has put out a notice of funding opportunity (NOFO) Global Infectious Disease Research Training Program (D43, Clinical Trial Optional), calling for applications for collaborative training programs that will strengthen the capacity of LMIC institutions to carry out infectious disease research (not including HIV/AIDS). 

The primary aim of this initiative is to cultivate scientific knowledge and skills among trainees from LMICs, thereby strengthening the research capacity of institutions in these countries to investigate methods for preventing, treating, and controlling infectious diseases that pose significant health risks. This announcement encourages joint applications from LMICs and U.S. research institutions.  

Research Objectives and Scope 

The objectives of the Global Infectious Disease Research Training program are as follows: 

  • To develop research training opportunities and professional development activities for a collaborative group of LMIC scientists and health research professionals at an LMIC institution to strengthen its capacity to conduct independent, sustainable infectious disease research. 
  • To provide mentored infectious disease research experience that is directly relevant to the health priorities of the LMIC of the trainees. 
  • To strengthen the capabilities of trainees at the proposed LMIC institution to lead, manage, and train others in infectious disease research. 

This NOFO can support research training related to infectious disease prevention, care, and treatment in a broad range of technical areas including: 

  • Basic, epidemiologic, clinical, behavioral, and social science research 
  • Bioengineering 
  • Bioinformatics, biostatistics, disease modeling 
  • Genetics/genomics 
  • Vector biology 
  • Pathophysiology, diagnostics, and therapeutics research 
  • Implementation, health economics, health services and systems research  
  • Clinical trials 

Applicants are also encouraged to design multidisciplinary research training programs with a focus on a global infectious disease cross-cutting theme.  

Note, however, that this program does not support HIV/AIDS research training. Applicants interested in HIV research training should apply to the FIC HIV Research Training Program Funding Opportunities

Award and Deadline Information  

Application budgets are limited to $230,000 per year for new awards and $276,000 per year for renewal awards (total direct costs). The maximum project period allowed is 5 years.  

Awards may provide stipends as a subsistence allowance to help defray living expenses during research training. They may also support the cost of tuition and fees at the rate already in place at U.S. or foreign institutions. Trainees may be paid a stipend comparable to their professional experience and U.S. or foreign institutional requirements. Refer to the NOFO for additional information on trainee travel and training related expenses.  

Non-domestic (non-U.S.) entities (foreign organizations) are eligible to apply, but non-domestic components of U.S. organizations are not eligible to apply.

Note, though, that only individuals who are citizens of LMICs (defined by the World Bank classification system) are eligible for research training support or other training activities. Individuals who have dual citizenship or permanent residency in the United States, other high-income countries, or ineligible countries as described in the NOFO are not eligible for training support. 

Be aware that the NOFO lists out specific instructions for how you should complete the budget section of your application. It also describes required International Training Data Tables.  

Note that clinical trials are optional, however, for applications proposing training in clinical trials, the recruitment and selection plans should include specific strategies to identify trainees who have the potential to organize, manage, and implement clinical trials. 

For applications proposing training in clinical trials research, remember to include plans for training in data management and statistics relevant to clinical trials, good clinical practice (GCP), and good laboratory practice (GLP). Also provide documentation of the administrative, data coordinating, enrollment, and laboratory or testing centers, appropriate for the clinical trial at the training sites. 

Contacts 

For questions related to your application, contact Dr. Barbara Sina at the Fogarty International Center at sinab@mail.nih.gov or 301-402-9467, or Dr. Stephanie Coomes at stephanie.coomes@nih.gov or 301-761-6855.

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