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Human Immunodeficiency Virus (HIV)

Infectious Diseases
21
Pipeline Programs
15
Companies
20
Clinical Trials
3 recruiting
1
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
9
1
1
0
6
4
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
250%
Monoclonal Antibody
125%
Vaccine
125%
+ 25 programs with unclassified modality

Infectious Diseases is an $11.9B market dominated by HIV and hepatitis C treatments in their peak revenue phases, reflecting a mature but stable therapeutic area.

$11.9B marketMature→ Stable30 products15 companies

Key Trends

  • HIV antiretroviral dominance: Nucleoside Reverse Transcriptase Inhibitors account for 44% of spending
  • Patent cliff pressure: $2.8B in revenue from major products facing LOE between 2027–2031
  • High trial velocity: 9,337 active trials indicate sustained pipeline development despite market maturity

Career Verdict

Infectious Diseases offers stable, well-compensated roles with strong commercial demand, but limited growth upside—ideal for risk-averse professionals seeking established franchises rather than high-growth opportunities.

AI-generated market analysis based on FDA, CMS, ClinicalTrials.gov, and hiring data

Market Leaders

#1BIKTARVYStable
$3.2B
Gilead Sciences·Peak10.5yr
#2EPCLUSAStable
$877M
Gilead Sciences·Peak8.1yr
#3TIVICAYDeclining
$657M
GSK·Peak4.1yr
#4TRIUMEQDeclining
$632M
GSK·Peak4.1yr
#5GENVOYAStable
$626M
Gilead Sciences·Peak6.9yr

Drug Class Breakdown

Nucleoside Reverse Transcriptase Inhibitors
$5.2B(44%)

backbone of HIV treatment, stable demand

RNA Replicase Inhibitors
$1.8B(15%)

hepatitis C treatment, mature market

Cytochrome P450 3A Inhibitors
$1.4B(12%)

boosting agents in combination regimens

P-Glycoprotein Inhibitors
$343M(3%)

niche mechanism, limited growth

Career Outlook

Stable

Infectious Diseases offers predictable career progression and above-average compensation in Commercial roles, supported by 780 current openings and sustained demand from market incumbents. However, patent cliffs affecting $2.8B in near-term revenue (2027–2031) will compress margins and slow hiring after 2028, particularly in Commercial support and field-based roles. The area is best suited for mid-career professionals seeking stability over rapid growth, with limited appeal for early-career scientists pursuing innovation-driven research.

Breaking In

Enter via Commercial or Manufacturing roles at GSK, Sanofi, or Becton Dickinson to build market expertise and commanding salaries ($160K–$237K); avoid pure R&D tracks unless you target specific mechanisms like long-acting injectables.

For Experienced Professionals

Experienced professionals should pursue Market Access, Medical Affairs, or Commercial Leadership roles where patent cliff expertise commands premium compensation; consider consulting or biotech transition if R&D innovation is your priority.

In-Demand Skills

Market access and payer strategyBrand management in generic-transition environmentsManufacturing scale-up and supply chain optimizationMedical science liaison (MSL) capabilities for physician engagementHealth economics and real-world outcomes analysis

Best For

Brand ManagerMarket Access ManagerMedical Science LiaisonSales DirectorManufacturing EngineerHealth Economics Analyst

Hiring Landscape

$160K–$275K

Infectious Diseases hiring is heavily weighted toward Commercial roles (247 positions, 32% of total), reflecting mature market dynamics focused on market access and brand management. GSK and Becton Dickinson lead hiring (214 and 188 roles), but Gilead Sciences—the market leader by revenue—shows surprisingly low hiring (25 roles), signaling efficiency-driven operations. Salary progression favors Commercial ($275K avg) over R&D ($184K avg), indicating career acceleration through sales and marketing functions.

780
Open Roles
5
Companies Hiring
4
Departments

Top Hiring Companies

214Growing
100Stable
61Stable
51Growing

By Department

Commercial(32%)
$275K
Engineering(16%)
$237K
Manufacturing(14%)
$160K
Research & Development(9%)
$184K

Strong Commercial hiring with premium salaries suggests Infectious Diseases is an excellent landing spot for brand, sales, and market access professionals, but limited R&D hiring indicates reduced innovation investment.

On Market (1)

Approved therapies currently available

GSK
SELZENTRYApproved
maraviroc
GSK
CCR5 Co-receptor Antagonist [EPC]oral2016
9M Part D

Competitive Landscape

13 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
5 programs
1
3
1
RaltegravirPhase 4Small Molecule
Doravirine, Tenofovir, LamivudinePhase 3
MK-8527Phase 3
MK-8527Phase 3
MK-8527Phase 1
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
5 programs
1
3
1
RaltegravirPhase 4Small Molecule1 trial
Doravirine, Tenofovir, LamivudinePhase 31 trial
MK-8527Phase 31 trial
MK-8527Phase 31 trial
MK-8527Phase 11 trial
Active Trials
NCT06783192Completed14Est. Oct 2023
NCT02403674Completed734Est. Sep 2023
NCT07044297Recruiting4,390Est. Jul 2027
+2 more trials
GSK
GSKLONDON, United Kingdom
2 programs
1
Open Label Treatment Access: MaravirocN/A1 trial
MaravirocPHASE_41 trial
Active Trials
NCT00992654No Longer Available
NCT01449006Completed19Est. Sep 2014
ViiV Healthcare
ViiV HealthcareNC - Durham
2 programs
1
MaravirocPhase 4
Open Label Treatment Access: MaravirocN/A
Colorado Therapeutics
Colorado TherapeuticsCO - Louisville
3 programs
1
Quadrivalent Live Attenuated Influenza VaccinePhase 2Vaccine1 trial
Dolutegravir Sodium MonohydrateN/A1 trial
Mitochondria in HIV and Aging (MITO+)N/A1 trial
Active Trials
NCT02028819No Longer AvailableEst. Feb 2014
NCT03489421Completed14Est. Sep 2019
NCT02474901Completed101Est. Dec 2016
Sangamo Therapeutics
1 program
1
SB-728mR-TPhase 1/21 trial
Active Trials
NCT02225665Completed8Est. Jun 2018
AbbVie
AbbVieNORTH CHICAGO, IL
3 programs
3
ABBV-181Phase 11 trial
ABBV-382Phase 11 trial
BudigalimabPhase 1Monoclonal Antibody2 trials
Active Trials
NCT04223804Completed41Est. Feb 2023
NCT04554966Completed54Est. Aug 2023
NCT05005403Recruiting694Est. Jul 2027
+1 more trials
Pfizer
PfizerNEW YORK, NY
2 programs
1
PF-04776548Phase 11 trial
Open Label Treatment Access: MaravirocN/A
Active Trials
NCT01045317Completed10Est. Feb 2010
Allergy Therapeutics
Allergy TherapeuticsUK - West Sussex
2 programs
2
3% w/w SPL7013 GelPhase 1
A244Phase 11 trial
Active Trials
NCT05423418Completed65Est. Oct 2024
Starpharma
StarpharmaAustralia - Abbotsford
1 program
1
3% w/w SPL7013 GelPhase 11 trial
Active Trials
NCT00370357Completed36Est. Jun 2007
Purdue Pharma
Purdue PharmaCT - Stamford
1 program
e-HERO: Ending the HIV Epidemic in Rural OklahomaN/A1 trial
Active Trials
NCT05664802Completed200Est. Jun 2024
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
MK-8527PHASE_1
CytoDyn
CytoDynVANCOUVER, WA
1 program
PRO 140PHASE_2_31 trial
Active Trials
NCT02990858Terminated43Est. Jul 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
GSKMaraviroc
Sharp TherapeuticsRaltegravir
Sharp TherapeuticsMK-8527
Sharp TherapeuticsMK-8527
Sharp TherapeuticsDoravirine, Tenofovir, Lamivudine
CytoDynPRO 140
Colorado TherapeuticsQuadrivalent Live Attenuated Influenza Vaccine
Sangamo TherapeuticsSB-728mR-T
Sharp TherapeuticsMK-8527
Allergy TherapeuticsA244
AbbVieBudigalimab
AbbVieABBV-382
AbbVieBudigalimab
AbbVieABBV-181
PfizerPF-04776548

Showing 15 of 19 trials with date data

Clinical Trials (20)

Total enrollment: 11,042 patients across 20 trials

A Study of the Neurological Effects of Adding Maraviroc to HAART Regimen in Patients With HIV (HANDmac)

Start: Oct 2011Est. completion: Sep 201419 patients
Phase 4Completed

A Study of the Neurological Effects of Adding Raltegravir to HAART Regimen in Patients With HIV

Start: Oct 2011Est. completion: Oct 20136 patients
Phase 4Terminated

A Study of MK-8527 to Prevent Human Immunodeficiency Virus Type 1 (HIV-1) (MK-8527-010)

Start: Nov 2025Est. completion: Oct 20274,580 patients
Phase 3Recruiting

A Clinical Study of MK-8527 to Prevent Human Immunodeficiency Virus Type 1 (HIV-1) (MK-8527-011)

Start: Jul 2025Est. completion: Jul 20274,390 patients
Phase 3Recruiting
NCT02403674Sharp TherapeuticsDoravirine, Tenofovir, Lamivudine

Comparison of Doravirine, Tenofovir, Lamivudine (MK-1439A) and ATRIPLA™ in Treatment-Naive Human Immunodeficiency Virus Type 1 (HIV-1)-Infected Participants (MK-1439A-021)

Start: Jun 2015Est. completion: Sep 2023734 patients
Phase 3Completed

An Extension Protocol for Subjects Who Successfully Completed PRO140_CD02 or PRO140_CD02_Open Label Study

Start: Nov 2016Est. completion: Jul 202243 patients
Phase 2/3Terminated
NCT02474901Colorado TherapeuticsQuadrivalent Live Attenuated Influenza Vaccine

Shedding, Immunogenicity and Safety of Quadrivalent Live Intranasal Influenza Vaccine (QLAIV) in HIV-infected Children and Young Adults

Start: Jul 2013Est. completion: Dec 2016101 patients
Phase 2Completed

Repeat Doses of SB-728mR-T After Cyclophosphamide Conditioning in HIV-Infected Subjects on HAART

Start: Aug 2014Est. completion: Jun 20188 patients
Phase 1/2Completed

A Drug-Drug Interaction Study of MK 8527 With a Combined Oral Contraceptive (LNG/EE)

Start: Aug 2023Est. completion: Oct 202314 patients
Phase 1Completed

Safety, Tolerability, and Immunogenicity of ALFQ in a HIV Vaccine Containing A244 and B.65321 in Healthy Adults

Start: Sep 2022Est. completion: Oct 202465 patients
Phase 1Completed

Study to Assess Adverse Events and Pharmacokinetics in Adult Participants With Non-Small Cell Lung Cancer, Head and Neck Squamous Cell Carcinoma and Other Solid Tumors, Receiving Intravenous Infusion of Azirkitug Alone or in Combination(s) With Budigalimab, Bevacizumab, or Telisotuzumab Adizutecan

Start: Nov 2021Est. completion: Jul 2027694 patients
Phase 1Recruiting

Study to Assess Adverse Events and How Intravenous (IV) or Subcutaneous (SC) ABBV-382 Moves Through the Body of Adult Participants With Human Immuno-Deficiency Virus (HIV-1)

Start: Apr 2021Est. completion: Aug 202354 patients
Phase 1Completed

Study to Evaluate the Safety and How the Body Handles a Single Dose of Subcutaneous (SC) and Intravenous (IV) Budigalimab in Adult Participants Living With Human Immunodeficiency Virus (HIV)

Start: Mar 2021Est. completion: Oct 202233 patients
Phase 1Completed

A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-181 (Budigalimab) in Adult Participants With Human Immunodeficiency Virus (HIV)-1

Start: Jan 2020Est. completion: Feb 202341 patients
Phase 1Completed

A Study To Investigate The Clearance Of PF-04776548 From The Body Following A Very Low (Micro) Dose Of The Compound Using A Low Level Of Radiotracer To Help Quantify Expected Low Concentrations Of PF-04776548 In The Body

Start: Jan 2010Est. completion: Feb 201010 patients
Phase 1Completed
NCT00370357Starpharma3% w/w SPL7013 Gel

SPL7013 Gel - Male Tolerance Study

Start: Aug 2006Est. completion: Jun 200736 patients
Phase 1Completed
NCT00992654GSKOpen Label Treatment Access: Maraviroc

A Treatment Access Program To Provide Maraviroc To Eligible Adult Patients Completing A4001050 Study Until Commercial Availability Of Maraviroc (Celsentri) In India

N/ANo Longer Available
NCT05664802Purdue Pharmae-HERO: Ending the HIV Epidemic in Rural Oklahoma

e-HERO: Ending the HIV Epidemic in Rural Oklahoma

Start: Dec 2022Est. completion: Jun 2024200 patients
N/ACompleted
NCT03489421Colorado TherapeuticsMitochondria in HIV and Aging (MITO+)

Mitochondria in HIV and Aging (MITO+)

Start: Dec 2018Est. completion: Sep 201914 patients
N/ACompleted
NCT02028819Colorado TherapeuticsDolutegravir Sodium Monohydrate

Compassionate Use of Ibalizumab for the Treatment of HIV Infection

Start: Jan 2012Est. completion: Feb 2014
N/ANo Longer Available

Related Jobs in Infectious Diseases

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

6 late-stage (Phase 3) programs, potential near-term approvals
3 actively recruiting trials targeting 11,042 patients
15 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.