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ACTG

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uuid002kdf1

Namestring
ACTG
Legal namestring
ACTG (AIDS Clinical Trials Group)
Websiteurl
actgnetwork.org
Company typeenum
Private
Founded yearint
1987
Descriptiontext

ACTG (AIDS Clinical Trials Group) is a global, nonprofit clinical trials network founded in 1987 and headquartered at the University of North Carolina at Chapel Hill School of Medicine, focused on advancing the management and cure of HIV and related infectious diseases. The network conducts Phase 1-4 clinical trials across 65 Clinical Research Sites in 15 countries on four continents, organized around five Transformative Science Groups (Antiretroviral Therapy, HIV Cure, Tuberculosis, Comorbidities, and Viral Hepatitis) plus cross-cutting groups in Behavioral Science, Women's Health, Neurology, and Implementation Science. ACTG's infrastructure is delivered through a consortium model: the Leadership and Operations Center (LOC) at UNC Chapel Hill, Statistical and Data Analysis Center at Harvard T.H. Chan School of Public Health, Data Management Center at Frontier Science Foundation, and Network Coordinating Center at DLH, supported by a network of specialty virology, immunology, and pharmacology laboratories and a Central Specimen Repository operated jointly with the IMPAACT network.

Since its founding, ACTG has enrolled 47,000+ participants across 3,000+ trials, with active studies targeting long-acting injectable antiretroviral regimens, HIV cure strategies (including a Small Clinical Trials Unit for intensive experimental studies), tuberculosis treatment-shortening regimens, hepatitis B therapeutics, and platform trials for emerging infectious diseases such as COVID-19 and mpox. Landmark outputs include the LATITUDE study published in the New England Journal of Medicine in 2026, which led to early trial halt after demonstrating the superiority of long-acting injectable cabotegravir and rilpivirine over daily oral ART in adherence-challenged populations.

ACTG is primarily funded by the NIH National Institute of Allergy and Infectious Diseases (NIAID) — through its Division of AIDS (DAIDS) — with collaborating support from the NIH National Institute of Mental Health (NIMH) and industry partners including ViiV Healthcare, Johnson & Johnson, and CIPLA, which supply investigational medications and co-fund specific protocols. The network monetizes through cooperative-agreement grant funding rather than commercial product sales; clinical trial participation is free for volunteers. Pharmaceutical sponsors gain access to ACTG's pre-established regulatory, laboratory, statistical, and site infrastructure, while the network's Global Community Advisory Board, Community Scientific Subcommittee, and site-level Community Advisory Boards ensure participant representation across the research lifecycle.

Short descriptiontext

ACTG is a nonprofit, NIH/NIAID-funded global clinical trials network conducting Phase 1-4 studies on HIV, tuberculosis, hepatitis, and emerging infectious diseases across 65 sites in 15 countries, having enrolled 47,000+ participants in 3,000+ trials since 1987.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBirmingham, United States
HQ citystring
Birmingham
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices11 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical trials network, HIV research studies, infectious disease research, clinical trial infrastructure, antiretroviral therapy research
Industry4 codes
1Clinical Development (Phase I–III Trial Design & Execution)
CodeHLAIALAEPrimaryYes
2Clinical Trial Site Operations & Study Coordination
CodeHLAGACAEPrimaryNo
3Healthcare Outcomes & Real-World Evidence (RWE) Analytics
CodeBPAHALANPrimaryNo
4Point-of-Care & Decentralized Trial Testing Services
CodeHLAGAEAKPrimaryNo
NAICS code3 codes
  • Scientific Research and Development Services5417
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Medical and Diagnostic Laboratories62151
SIC code3 codes
  • Services-Commercial Physical & Biological Research8731
  • Services-Misc Health & Allied Services, Nec8090
  • Services-Medical Laboratories8071
Product category
Clinical Trials Network Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1NIH/NIAID Government Funding
TypeSubscription Recurring
Description

ACTG is primarily funded by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH), and collaborating NIH institutes including the National Institute of Mental Health. This constitutes the core operational funding for the network's clinical trials infrastructure, site management, laboratory operations, and scientific agenda.

actgnetwork.org
2Industry Support / Pharmaceutical Partnerships
TypeLicensing Royalties
Description

Pharmaceutical companies including ViiV Healthcare, Johnson & Johnson, and CIPLA provide medications, product support, or co-funding for specific clinical trials. Medications for studies are sometimes provided by pharmaceutical partners, such as cabotegravir and rilpivirine provided by ViiV Healthcare and Johnson & Johnson for the LATITUDE study.

financialpost.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Technology or R&D, Infrastructure, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1Small Clinical Trials Advancing HIV Remission and Cure
Description

A program under ACTG's Cure Transformative Science Group for conducting small experimental clinical trials (less than 30 participants) to advance HIV remission and cure efforts.

actgnetwork.org
Core offering1 text field

ACTG conducts Phase 1–4 clinical trials for HIV, tuberculosis, hepatitis B, and emerging infectious diseases through a global network of 65 Clinical Research Sites in 15 countries on four continents. The network provides full trial infrastructure — protocol development, statistical and data management support, specialty laboratories, specimen repositories, and regulatory liaison — organized around five Transformative Science Groups (Antiretroviral Therapy, HIV Cure, Tuberculosis, Comorbidities, Viral Hepatitis) plus cross-cutting groups in Behavioral Science, Women's Health, Neurology, and Implementation Science. Pharmaceutical partners and academic investigators use ACTG's pre-established platform to evaluate novel therapies; clinical trial participation is free for volunteers.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Long-acting injectable cabotegravir and rilpivirine reduced the cumulative risk of regimen failure at 48 weeks by nearly half — 22.8% for Cabenuva versus 41.2% for daily oral ART — leading to early halting of the LATITUDE trial in February 2024.
+4 more records
Product overview1 text field

ACTG (AIDS Clinical Trials Group) is the world's largest and longest-running clinical trials network focused on HIV and infectious diseases. Founded in 1987, ACTG operates a portfolio of clinical studies including HIV cure research, antiretroviral therapy optimization, treatment for comorbidities, tuberculosis, hepatitis, and emerging infectious diseases. The network comprises thousands of researchers across 65 clinical research sites in 15 countries on four continents, having conducted over 3,000 trials. Key research programs include the Small Clinical Trials Advancing HIV Remission and Cure program, transformative science groups focused on antiretroviral therapy, HIV cure, tuberculosis, comorbidities, viral hepatitis, and cross-cutting groups in behavioral science, women's health, neurology, and implementation science.

Product and service4 records
1ACTG Clinical Trials Network
CategoryClinical Trials Network
Description

The ACTG Clinical Trials Network is the world's largest HIV clinical trials network, conducting research to improve the management of HIV and its comorbidities, develop cures for HIV, and innovate treatments for tuberculosis, hepatitis B, and emerging infectious diseases. The network operates 65 sites across 15 countries on four continents with 47,000+ participants and 3,000+ trials conducted since 1987, used by pharmaceutical companies and academic investigators.

2Small Clinical Trials Advancing HIV Remission and Cure Program
CategoryClinical Trials Program
Description

A specialized program for conducting small (less than 30 participants), intensive experimental clinical trials to advance HIV remission and cure efforts using ACTG's infrastructure. Managed by the ACTG Small Clinical Trials Unit (SCTU). The first study under this program is Study A5413 evaluating oral dasatinib.

3ACTG Specimen Repository
CategoryBiospecimen Resource
Description

A large body of specimens collected from ACTG and IMPAACT network studies, available to investigators through a standard application and review process. Specimens are stored at the Central Specimen Repository managed by the Biomedical Research Institute. Used by academic investigators for HIV and infectious disease research.

4HIV Databases
CategoryResearch Data Resource
Description

ACTG provides access to HIV databases for researchers to support data analysis and cross-study research. Used by academic and clinical investigators conducting secondary analyses.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership9 partners
Strategic tierKeyTypeStrategic or Co-development Partner
Description

ViiV Healthcare provides cabotegravir and rilpivirine medications for ACTG's LATITUDE study (A5359), which demonstrated the superiority of long-acting injectable Cabenuva over daily oral ART in people with adherence challenges. ViiV is a specialist HIV company jointly owned by GSK and Pfizer.

Strategic tierKeyTypeStrategic or Co-development Partner
Description

Johnson & Johnson provides medications (cabotegravir + rilpivirine) for the LATITUDE study as part of a collaboration with ViiV Healthcare. The study was funded by NIH with medications provided by ViiV Healthcare and Johnson & Johnson.

Strategic tierSupportingTypeStrategic or Co-development Partner
Description

CIPLA provides industry support for study A5402 (COPE), a phase 2 randomized clinical trial evaluating pramipexole versus escitalopram for treating depressive disorders and mild neurocognitive disorder among people living with HIV.

Strategic tierKeyTypeStrategic or Co-development Partner
Description

The Statistical and Data Analysis Center (SDAC) is housed at Harvard T.H. Chan School of Public Health, providing complete statistical support from study design through publication for ACTG Phase 1-4 clinical trials. Harvard biostatisticians are core members of each protocol team.

Strategic tierCore/FundamentalTypeStrategic or Co-development Partner
Description

The Leadership and Operations Center (LOC) Administrative Core is housed within UNC Chapel Hill's School of Medicine and Clinical Research Alliance. Responsible for managing all network funds, developing/negotiating budgets and contracts, supporting network meetings, and coordinating external communications.

Strategic tierKeyTypeStrategic or Co-development Partner
Description

Frontier Science Foundation acts as the ACTG Data Management Center (DMC), facilitating design and development of electronic case report forms, monitoring data quality, and preparing data for FDA progress reports. Also partners on the Repository Advisory Group (RAG) for specimen management.

Strategic tierKeyTypeStrategic or Co-development Partner
Description

The Network Coordinating Center (NCC) is housed at DLH and collaborates with ACTG leadership to provide technical, scientific, administrative, and project management support. NCC coordinates implementation of the scientific research agenda and ensures compliance with network policies among ACTG leadership, sites, and partners.

Strategic tierKeyTypeStrategic or Co-development Partner
Description

The Repository Advisory Group (RAG) is a collaboration between ACTG and IMPAACT clinical trials networks to make specimens collected from network studies available to investigators. This partnership creates a combined specimen repository spanning two major HIV/AIDS clinical trials networks.

Strategic tierSupportingTypeStrategic or Co-development Partner
Description

The Central Specimen Repository managed by the Biomedical Research Institute stores specimens collected from completed ACTG and IMPAACT studies, making them available to investigators for new research through standard application and review processes.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
1INSIGHT Network
TypeDirect peer
Description

International Network for Strategic Initiatives in Global HIV Trials — NIH-funded HIV and emerging-infection trials network conducting large, pragmatic Phase 3/4 studies. Comparable in operating model (NIH cooperative agreement, multicenter global CRS model) and therapeutic focus areas (HIV, COVID-19).

TypeDirect peer
Description

International Maternal Pediatric Adolescent AIDS Clinical Trials Network — directly comparable NIH/DAIDS-funded HIV clinical trials network focused on maternal/pediatric HIV, TB, and pregnancy; partner with ACTG on the Central Specimen Repository, making them the closest functional peer.

3Tuberculosis Trials Consortium (TBTC)
TypeDirect peer
Description

CDC-sponsored consortium conducting Phase 2/3 TB treatment and prevention trials across US and international sites. Most directly comparable to ACTG's TB TSG work and shares the multi-site, federally-funded clinical trial operations model.

TypeDirect peer
Description

NIH-funded network conducting clinical trials of microbicides for HIV prevention. Operates with a similar DAIDS consortium structure, multicenter site network, and community engagement model, although narrower in scope (prevention only).

TypeDirect peer
Description

NIAID-funded HIV clinical trials network focused on prevention research (PrEP, vaccines, microbicides). Operates with analogous multi-site, NIH-funded, Phase 1-4 trial infrastructure serving overlapping investigator and pharmaceutical partner communities.

TypeBroad incumbent
Description

Global commercial contract research organization (CRO) providing clinical trial operations, laboratory, and data services. Operates at vastly larger scale than ACTG in commercial trials, with overlapping capabilities in trial design, biostatistics, central labs, and site management used by ACTG's pharmaceutical sponsors.

TypeDirect peer
Description

NIAID-funded HIV vaccine clinical trials network operating global CRS sites and similar immunological laboratory infrastructure. Comparable in governance model, funder relationship, and operational scale to ACTG, though focused on vaccine efficacy rather than therapeutic/cure research.

TypeBroad incumbent
Description

Major CRO and research models organization providing preclinical and clinical laboratory services, including specialty lab capabilities (virology, immunology, pharmacology) that mirror the scope of ACTG's specialty laboratory network (Pitt, Emory, UNC, UCSD/SDSU).

TypeBroad incumbent
Description

Global CRO providing clinical research, laboratory, and consulting services to pharma/biotech. Comparable through its central lab (formerly PRA) and post-2017 PRA merger that delivers similar data management, biostatistics, and global site support functions to ACTG's network infrastructure.

TypeBroad incumbent
Description

Large global CRO offering Phase I-IV clinical trial management, central labs, and bioservices acquired from PPD. Comparable in delivering centralized biostatistics, data management, and lab services that parallel ACTG's SDAC, DMC, and specialty lab functions.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment6 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile4 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles21 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

ACTG

Clinical Trials Network Servicesactgnetwork.org

ACTG is a nonprofit, NIH/NIAID-funded global clinical trials network conducting Phase 1-4 studies on HIV, tuberculosis, hepatitis, and emerging infectious diseases across 65 sites in 15 countries, having enrolled 47,000+ participants in 3,000+ trials since 1987.

What ACTG does

ACTG (AIDS Clinical Trials Group) is a global, nonprofit clinical trials network founded in 1987 and headquartered at the University of North Carolina at Chapel Hill School of Medicine, focused on advancing the management and cure of HIV and related infectious diseases. The network conducts Phase 1-4 clinical trials across 65 Clinical Research Sites in 15 countries on four continents, organized around five Transformative Science Groups (Antiretroviral Therapy, HIV Cure, Tuberculosis, Comorbidities, and Viral Hepatitis) plus cross-cutting groups in Behavioral Science, Women's Health, Neurology, and Implementation Science. ACTG's infrastructure is delivered through a consortium model: the Leadership and Operations Center (LOC) at UNC Chapel Hill, Statistical and Data Analysis Center at Harvard T.H. Chan School of Public Health, Data Management Center at Frontier Science Foundation, and Network Coordinating Center at DLH, supported by a network of specialty virology, immunology, and pharmacology laboratories and a Central Specimen Repository operated jointly with the IMPAACT network.

Since its founding, ACTG has enrolled 47,000+ participants across 3,000+ trials, with active studies targeting long-acting injectable antiretroviral regimens, HIV cure strategies (including a Small Clinical Trials Unit for intensive experimental studies), tuberculosis treatment-shortening regimens, hepatitis B therapeutics, and platform trials for emerging infectious diseases such as COVID-19 and mpox. Landmark outputs include the LATITUDE study published in the New England Journal of Medicine in 2026, which led to early trial halt after demonstrating the superiority of long-acting injectable cabotegravir and rilpivirine over daily oral ART in adherence-challenged populations.

ACTG is primarily funded by the NIH National Institute of Allergy and Infectious Diseases (NIAID) — through its Division of AIDS (DAIDS) — with collaborating support from the NIH National Institute of Mental Health (NIMH) and industry partners including ViiV Healthcare, Johnson & Johnson, and CIPLA, which supply investigational medications and co-fund specific protocols. The network monetizes through cooperative-agreement grant funding rather than commercial product sales; clinical trial participation is free for volunteers. Pharmaceutical sponsors gain access to ACTG's pre-established regulatory, laboratory, statistical, and site infrastructure, while the network's Global Community Advisory Board, Community Scientific Subcommittee, and site-level Community Advisory Boards ensure participant representation across the research lifecycle.

ACTG firmographics

Firmographics
Name
ACTG
Legal name
ACTG (AIDS Clinical Trials Group)
Website
https://actgnetwork.org
Company type
Private
Founded year
1987
Operating status
Operating
Headcount range
11–50 employees
Short description
ACTG is a nonprofit, NIH/NIAID-funded global clinical trials network conducting Phase 1-4 studies on HIV, tuberculosis, hepatitis, and emerging infectious diseases across 65 sites in 15 countries, having enrolled 47,000+ participants in 3,000+ trials since 1987.
Ownership category
akta.pro rank

ACTG industry classification

Industry
Product category
Clinical Trials Network Services
NAICS
Scientific Research and Development Services (5417), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Medical and Diagnostic Laboratories (62151)
SIC
Services-Commercial Physical & Biological Research (8731), Services-Misc Health & Allied Services, Nec (8090), Services-Medical Laboratories (8071)
akta.pro primary industry
Clinical Development (Phase I–III Trial Design & Execution) (HLAIALAE)
akta.pro secondary industries
Clinical Trial Site Operations & Study Coordination (HLAGACAE), Healthcare Outcomes & Real-World Evidence (RWE) Analytics (BPAHALAN), Point-of-Care & Decentralized Trial Testing Services (HLAGAEAK)

Keywords

  • Clinical trials network
  • HIV research studies
  • Infectious disease research
  • Clinical trial infrastructure
  • Antiretroviral therapy research

Where ACTG is headquartered

Location

Headquarters

HQ city
Birmingham
HQ country
United States
HQ region
North America

Offices11 records

Markets served

ACTG business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Technology or R&D, Infrastructure, Marketing or Sales

Revenue model

  1. NIH/NIAID Government Funding: ACTG is primarily funded by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH), and collaborating NIH institutes including the National Institute of Mental Health. This constitutes the core operational funding for the network's clinical trials infrastructure, site management, laboratory operations, and scientific agenda.
  2. Industry Support / Pharmaceutical Partnerships: Pharmaceutical companies including ViiV Healthcare, Johnson & Johnson, and CIPLA provide medications, product support, or co-funding for specific clinical trials. Medications for studies are sometimes provided by pharmaceutical partners, such as cabotegravir and rilpivirine provided by ViiV Healthcare and Johnson & Johnson for the LATITUDE study.

Go-to-market motion1 record

Distribution channels3 records

Marketing channels7 records

ACTG product offering

Product offering

Core offering

ACTG conducts Phase 1–4 clinical trials for HIV, tuberculosis, hepatitis B, and emerging infectious diseases through a global network of 65 Clinical Research Sites in 15 countries on four continents. The network provides full trial infrastructure — protocol development, statistical and data management support, specialty laboratories, specimen repositories, and regulatory liaison — organized around five Transformative Science Groups (Antiretroviral Therapy, HIV Cure, Tuberculosis, Comorbidities, Viral Hepatitis) plus cross-cutting groups in Behavioral Science, Women's Health, Neurology, and Implementation Science. Pharmaceutical partners and academic investigators use ACTG's pre-established platform to evaluate novel therapies; clinical trial participation is free for volunteers.

Product overview

ACTG (AIDS Clinical Trials Group) is the world's largest and longest-running clinical trials network focused on HIV and infectious diseases. Founded in 1987, ACTG operates a portfolio of clinical studies including HIV cure research, antiretroviral therapy optimization, treatment for comorbidities, tuberculosis, hepatitis, and emerging infectious diseases. The network comprises thousands of researchers across 65 clinical research sites in 15 countries on four continents, having conducted over 3,000 trials. Key research programs include the Small Clinical Trials Advancing HIV Remission and Cure program, transformative science groups focused on antiretroviral therapy, HIV cure, tuberculosis, comorbidities, viral hepatitis, and cross-cutting groups in behavioral science, women's health, neurology, and implementation science.

Differentiator

Problem solved

Functional benefit

Brands

  • Small Clinical Trials Advancing HIV Remission and Cure: A program under ACTG's Cure Transformative Science Group for conducting small experimental clinical trials (less than 30 participants) to advance HIV remission and cure efforts.

Products and services

  • ACTG Clinical Trials Network The ACTG Clinical Trials Network is the world's largest HIV clinical trials network, conducting research to improve the management of HIV and its comorbidities, develop cures for HIV, and innovate treatments for tuberculosis, hepatitis B, and emerging infectious diseases. The network operates 65 sites across 15 countries on four continents with 47,000+ participants and 3,000+ trials conducted since 1987, used by pharmaceutical companies and academic investigators.
  • Small Clinical Trials Advancing HIV Remission and Cure Program A specialized program for conducting small (less than 30 participants), intensive experimental clinical trials to advance HIV remission and cure efforts using ACTG's infrastructure. Managed by the ACTG Small Clinical Trials Unit (SCTU). The first study under this program is Study A5413 evaluating oral dasatinib.
  • ACTG Specimen Repository A large body of specimens collected from ACTG and IMPAACT network studies, available to investigators through a standard application and review process. Specimens are stored at the Central Specimen Repository managed by the Biomedical Research Institute. Used by academic investigators for HIV and infectious disease research.
  • HIV Databases ACTG provides access to HIV databases for researchers to support data analysis and cross-study research. Used by academic and clinical investigators conducting secondary analyses.

Quantifiable outcome

  • Long-acting injectable cabotegravir and rilpivirine reduced the cumulative risk of regimen failure at 48 weeks by nearly half — 22.8% for Cabenuva versus 41.2% for daily oral ART — leading to early halting of the LATITUDE trial in February 2024.
  • +4 more outcomes

Companies that use ACTG

Customer profile

Named customers4 records

Segments6 records

Ideal customer profiles4 records

ACTG technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

ACTG partnerships and signals

Strategic signal

Partnerships

Nine partnerships are on record, tiered key, supporting and core/fundamental.

  • ViiV HealthcarekeyStrategic or Co-development PartnerViiV Healthcare provides cabotegravir and rilpivirine medications for ACTG's LATITUDE study (A5359), which demonstrated the superiority of long-acting injectable Cabenuva over daily oral ART in people with adherence challenges. ViiV is a specialist HIV company jointly owned by GSK and Pfizer.
  • Johnson & JohnsonkeyStrategic or Co-development PartnerJohnson & Johnson provides medications (cabotegravir + rilpivirine) for the LATITUDE study as part of a collaboration with ViiV Healthcare. The study was funded by NIH with medications provided by ViiV Healthcare and Johnson & Johnson.
  • CIPLAsupportingStrategic or Co-development PartnerCIPLA provides industry support for study A5402 (COPE), a phase 2 randomized clinical trial evaluating pramipexole versus escitalopram for treating depressive disorders and mild neurocognitive disorder among people living with HIV.
  • Harvard T.H. Chan School of Public HealthkeyStrategic or Co-development PartnerThe Statistical and Data Analysis Center (SDAC) is housed at Harvard T.H. Chan School of Public Health, providing complete statistical support from study design through publication for ACTG Phase 1-4 clinical trials. Harvard biostatisticians are core members of each protocol team.
  • University of North Carolina at Chapel Hillcore/fundamentalStrategic or Co-development PartnerThe Leadership and Operations Center (LOC) Administrative Core is housed within UNC Chapel Hill's School of Medicine and Clinical Research Alliance. Responsible for managing all network funds, developing/negotiating budgets and contracts, supporting network meetings, and coordinating external communications.
  • Frontier Science Foundation (FSTRF)keyStrategic or Co-development PartnerFrontier Science Foundation acts as the ACTG Data Management Center (DMC), facilitating design and development of electronic case report forms, monitoring data quality, and preparing data for FDA progress reports. Also partners on the Repository Advisory Group (RAG) for specimen management.
  • DLH (Network Coordinating Center)keyStrategic or Co-development PartnerThe Network Coordinating Center (NCC) is housed at DLH and collaborates with ACTG leadership to provide technical, scientific, administrative, and project management support. NCC coordinates implementation of the scientific research agenda and ensures compliance with network policies among ACTG leadership, sites, and partners.
  • IMPAACT Clinical Trials NetworkkeyStrategic or Co-development PartnerThe Repository Advisory Group (RAG) is a collaboration between ACTG and IMPAACT clinical trials networks to make specimens collected from network studies available to investigators. This partnership creates a combined specimen repository spanning two major HIV/AIDS clinical trials networks.
  • Biomedical Research Institute (Central Specimen Repository)supportingStrategic or Co-development PartnerThe Central Specimen Repository managed by the Biomedical Research Institute stores specimens collected from completed ACTG and IMPAACT studies, making them available to investigators for new research through standard application and review processes.

Scale indicators6 records

Recent moves6 records

Expansion highlights5 records

ACTG competitors and assessment

Company assessment

Direct peers

  • INSIGHT Network: International Network for Strategic Initiatives in Global HIV Trials — NIH-funded HIV and emerging-infection trials network conducting large, pragmatic Phase 3/4 studies. Comparable in operating model (NIH cooperative agreement, multicenter global CRS model) and therapeutic focus areas (HIV, COVID-19).
  • IMPAACT Network: International Maternal Pediatric Adolescent AIDS Clinical Trials Network — directly comparable NIH/DAIDS-funded HIV clinical trials network focused on maternal/pediatric HIV, TB, and pregnancy; partner with ACTG on the Central Specimen Repository, making them the closest functional peer.
  • Tuberculosis Trials Consortium (TBTC): CDC-sponsored consortium conducting Phase 2/3 TB treatment and prevention trials across US and international sites. Most directly comparable to ACTG's TB TSG work and shares the multi-site, federally-funded clinical trial operations model.
  • Microbicide Trials Network (MTN): NIH-funded network conducting clinical trials of microbicides for HIV prevention. Operates with a similar DAIDS consortium structure, multicenter site network, and community engagement model, although narrower in scope (prevention only).
  • HIV Prevention Trials Network (HPTN): NIAID-funded HIV clinical trials network focused on prevention research (PrEP, vaccines, microbicides). Operates with analogous multi-site, NIH-funded, Phase 1-4 trial infrastructure serving overlapping investigator and pharmaceutical partner communities.
  • HIV Vaccine Trials Network (HVTN): NIAID-funded HIV vaccine clinical trials network operating global CRS sites and similar immunological laboratory infrastructure. Comparable in governance model, funder relationship, and operational scale to ACTG, though focused on vaccine efficacy rather than therapeutic/cure research.

Broad incumbents

  • IQVIA: Global commercial contract research organization (CRO) providing clinical trial operations, laboratory, and data services. Operates at vastly larger scale than ACTG in commercial trials, with overlapping capabilities in trial design, biostatistics, central labs, and site management used by ACTG's pharmaceutical sponsors.
  • Charles River Laboratories: Major CRO and research models organization providing preclinical and clinical laboratory services, including specialty lab capabilities (virology, immunology, pharmacology) that mirror the scope of ACTG's specialty laboratory network (Pitt, Emory, UNC, UCSD/SDSU).
  • ICON plc: Global CRO providing clinical research, laboratory, and consulting services to pharma/biotech. Comparable through its central lab (formerly PRA) and post-2017 PRA merger that delivers similar data management, biostatistics, and global site support functions to ACTG's network infrastructure.
  • Thermo Fisher PPD (Clinical Research Services): Large global CRO offering Phase I-IV clinical trial management, central labs, and bioservices acquired from PPD. Comparable in delivering centralized biostatistics, data management, and lab services that parallel ACTG's SDAC, DMC, and specialty lab functions.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights6 records

Customer concentration

ACTG social profiles

Digital presence

ACTG financial estimates

Financial estimate

Revenue estimate

Valuation estimate

ACTG leadership team

Management profile

Number of profiles

Profiles21 records

ACTG funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

ACTG M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about ACTG

What does ACTG do?

ACTG conducts Phase 1–4 clinical trials for HIV, tuberculosis, hepatitis B, and emerging infectious diseases through a global network of 65 Clinical Research Sites in 15 countries on four continents. The network provides full trial infrastructure — protocol development, statistical and data management support, specialty laboratories, specimen repositories, and regulatory liaison — organized around five Transformative Science Groups (Antiretroviral Therapy, HIV Cure, Tuberculosis, Comorbidities, Viral Hepatitis) plus cross-cutting groups in Behavioral Science, Women's Health, Neurology, and Implementation Science. Pharmaceutical partners and academic investigators use ACTG's pre-established platform to evaluate novel therapies; clinical trial participation is free for volunteers.

Is ACTG a public or private company?

ACTG is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was ACTG founded?

ACTG was founded in 1987. It employs 11 to 50 people.

Where is ACTG based?

ACTG is headquartered in Birmingham, United States, in the North America region.

How does ACTG make money?

Two revenue lines are on record. NIH/NIAID Government Funding is the primary driver. The others are industry Support / Pharmaceutical Partnerships.

Who are ACTG's main competitors?

Direct peers on record are INSIGHT Network, IMPAACT Network, Tuberculosis Trials Consortium (TBTC), Microbicide Trials Network (MTN), HIV Prevention Trials Network (HPTN) and HIV Vaccine Trials Network (HVTN). Broad incumbents are IQVIA, Charles River Laboratories, ICON plc and Thermo Fisher PPD (Clinical Research Services).

Does ACTG have an API?

No public API is recorded for ACTG.

What industry is ACTG in?

ACTG's product category is Clinical Trials Network Services. Its primary akta.pro industry code is HLAIALAE, Clinical Development (Phase I–III Trial Design & Execution), with a secondary code of HLAGACAE, Clinical Trial Site Operations & Study Coordination. Its NAICS code is 5417 and its SIC code is 8731.

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BioSpaceACTG Launches HIV Cure Study Evaluating Novel Approach Targeting the HIV ReservoirACTG opened study A5413, a randomized, double-blind, placebo-controlled trial evaluating oral dasatinib's safety and impact on the HIV reservoir in people on antiretroviral therapy. The study enrolls 14 participants, randomizing them to 100 mg daily dasatinib or placebo for 12 weeks, followed by 24 weeks. It is the first study under ACTG's Small Clinical Trials Advancing HIV Remission and Cure program.GlobeNewswireACTG Launches HIV Cure Study Evaluating Novel Approach Targeting the HIV ReservoirACTG, the world's largest HIV clinical trials network, announced the launch of study A5413, a randomized double-blind placebo-controlled clinical trial evaluating oral dasatinib for its ability to reduce the HIV reservoir in 14 participants on antiretroviral therapy. The trial will treat participants with 100 mg daily dasatinib or placebo for 12 weeks, followed by 24 weeks of observation, and is the first study under ACTG's Small Clinical Trials Advancing HIV Remission and Cure program. Funded by the NIH's National Institute of Mental Health and NIAID, the study tests a novel approach of blocking CD4 cell proliferation to potentially shrink the latent HIV reservoir, addressing a major barrier to an HIV cure.Financial PostACTG Launches Landmark Study Evaluating Treatments for Depressive Disorders with or without Mild Neurocognitive Disorder among People Living with HIVACTG announced the launch of study A5402, a phase 2 randomized clinical trial evaluating pramipexole versus escitalopram for treating depressive disorders and mild neurocognitive disorder among people living with HIV. The multi-center trial will enroll 186 participants aged 18-70 across ACTG clinical research sites over a 24-week treatment period, sponsored by the NIH's National Institute of Mental Health and National Institute of Allergy and Infectious Diseases with industry support from CIPLA. The study addresses a condition affecting up to 80 percent of people living with HIV globally, representing a two- to four-fold increase compared to the general population.The Canadian Press NewsACTG Launches Landmark Study Evaluating Treatments for Depressive Disorders with or without Mild Neurocognitive Disorder among People Living with HIVACTG opened study A5402, a phase 2 trial comparing pramipexole to escitalopram for depressive disorders with or without mild neurocognitive disorder in people living with HIV. The trial will enroll 186 participants on ART for 24 weeks, aiming to see if pramipexole is more effective than standard antidepressants.GlobeNewswireACTG Launches Landmark Study Evaluating Treatments for Depressive Disorders with or without Mild Neurocognitive Disorder among People Living with HIVACTG opened study A5402, a phase 2 trial comparing pramipexole to escitalopram for depressive disorders with or without mild neurocognitive disorder in people living with HIV. The trial will enroll 186 participants on antiretroviral therapy, aiming to assess whether pramipexole is more effective than standard antidepressants.GlobeNewswireACTG Launches Critical Study Evaluating Hormone Therapy for Women Living with HIV in the Menopause TransitionACTG opened the HoT study (A5424), a phase 4 trial evaluating estradiol gel with or without oral progesterone versus placebo for women living with HIV in the menopausal transition. The trial enrolls 240 participants aged 40-60 with moderate to severe vasomotor symptoms, aiming to provide clinical guidance for midlife care.Financial PostACTG Announces Publication of STOMP Results in the New England Journal of MedicineACTG announced the publication of STOMP trial results in the New England Journal of Medicine, demonstrating that tecovirimat does not improve mpox resolution. The phase 3 trial involved 412 participants across seven countries and was stopped early after interim analysis showed no benefit in symptom resolution. These findings emphasize the necessity of conducting randomized controlled trials for mpox therapeutics.GlobeNewswireACTG Announces Publication of STOMP Results in the New England Journal of MedicineACTG published STOMP trial results in the New England Journal of Medicine, showing tecovirimat did not improve mpox resolution. The phase 3 trial of 412 participants found 79% resolution in the treatment group versus 81% in placebo, with no differences in pain or healing. The findings underscore the need for randomized trials to identify effective mpox therapeutics.GlobeNewswireACTG Announces Publication of STOMP Results in the New England Journal of MedicineACTG announced publication of STOMP trial results in the New England Journal of Medicine showing that tecovirimat did not improve mpox resolution compared to placebo in a phase 3 randomized controlled trial. The trial enrolled 412 participants across seven countries and found 79% of the tecovirimat group achieved clinical resolution by day 29 versus 81% in the placebo group, with no significant differences in pain reduction or other secondary endpoints. The findings underscore the need for continued randomized controlled trials to identify safe and effective therapeutics for mpox.Financial PostACTG Announces Publication of LATITUDE Findings in the New England Journal of MedicineACTG announced the publication of the LATITUDE study in the New England Journal of Medicine, which reports that long-acting injectable cabotegravir and rilpivirine was more effective than oral ART in preventing regimen failure among people living with HIV with adherence challenges. The study involved 453 participants and was halted early in February 2024 due to interim efficacy results showing significant benefit. The findings could expand the use of long-acting HIV treatment options.