Skip to main content

Human Papillomavirus Infection

15
Pipeline Programs
10
Companies
20
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
2
1
0
0
7
5
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Vaccine
7100%
+ 26 programs with unclassified modality

Competitive Landscape

10 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
7 programs
2
2
Diphtheria Toxoid/Tetanus Toxoid/Acellular Pertussis Vaccine AdsorbedPhase 4Vaccine1 trial
GardasilPhase 41 trial
V503Phase 31 trial
V503Phase 31 trial
ComplianceN/A1 trial
+2 more programs
Active Trials
NCT01087164Unknown600Est. Jun 2014
NCT00932009Completed1,933Est. Dec 2009
NCT00572832Completed200Est. Aug 2009
+4 more trials
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
7 programs
2
2
Diphtheria Toxoid/Tetanus Toxoid/Acellular Pertussis Vaccine AdsorbedPhase 4Vaccine
GardasilPhase 4
V503Phase 3
V503Phase 3
ComplianceN/A
+2 more programs
Merck & Co.
Merck & Co.RAHWAY, NJ
3 programs
1
Diphtheria Toxoid/Tetanus Toxoid/Acellular Pertussis Vaccine AdsorbedPhase 4Vaccine
Quadrivalent human papillomavirus vaccine on-time administrationN/AVaccine
offer of vaginal self collectionPHASE_2_31 trial
Active Trials
NCT01095198Unknown1,440Est. Jan 2013
Guard Therapeutics
Guard TherapeuticsSweden - Stockholm
4 programs
1
3
Nonavalent HPV study vaccinePhase 3Vaccine1 trial
Recombinant NonavalentPhase 31 trial
Recombinant NonavalentPhase 31 trial
Recombinant NonavalentPhase 11 trial
Active Trials
NCT05680454Completed160Est. May 2022
NCT06207175Unknown1,260Est. Jan 2026
NCT05668572Unknown12,000Est. Feb 2023
+1 more trials
Antiva Biosciences
Antiva BiosciencesCA - Redwood City
1 program
1
ABI-2280Phase 1/21 trial
Active Trials
NCT06491446Completed141Est. Apr 2026
BravoVax
BravoVaxChina - Wuhan
1 program
1
Human papillomavirusPhase 11 trial
Active Trials
NCT05672966Unknown40Est. Oct 2024
GSK
GSKLONDON, United Kingdom
4 programs
Cervarix data collectionN/A1 trial
Endocervical samplesN/A1 trial
Endocervical samplesN/A1 trial
Prevalence-based modelN/A1 trial
Active Trials
NCT01551537Withdrawn0Est. Apr 2014
NCT01205412Completed552Est. Nov 2011
NCT01158209Completed490Est. Aug 2011
+1 more trials
ViiV Healthcare
ViiV HealthcareNC - Durham
4 programs
Cervarix data collectionN/A
Endocervical samplesN/A
Endocervical samplesN/A
Prevalence-based modelN/A
Geneva Biotech
Geneva BiotechSwitzerland - Pregny-Chambésy
1 program
HPV testingN/A1 trial
Active Trials
NCT07550010Recruiting1,800Est. Sep 2027
Angeles Therapeutics
Angeles TherapeuticsCA - Los Angeles
1 program
Parent RemindersN/A1 trial
Active Trials
NCT03726151Completed17,000Est. May 2024

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
MSDDiphtheria Toxoid/Tetanus Toxoid/Acellular Pertussis Vaccine Adsorbed
MSDGardasil
Guard TherapeuticsNonavalent HPV study vaccine
Guard TherapeuticsRecombinant Nonavalent
Guard TherapeuticsRecombinant Nonavalent
MSDV503
MSDV503
Merck & Co.offer of vaginal self collection
Antiva BiosciencesABI-2280
BravoVaxHuman papillomavirus
Guard TherapeuticsRecombinant Nonavalent
Geneva BiotechHPV testing
Angeles TherapeuticsParent Reminders
GSKCervarix data collection
GSKEndocervical samples

Showing 15 of 20 trials with date data

Clinical Trials (20)

Total enrollment: 57,026 patients across 20 trials

NCT07706673MSDDiphtheria Toxoid/Tetanus Toxoid/Acellular Pertussis Vaccine Adsorbed

ESCUDDO Long Term Follow Up

Start: Aug 2026Est. completion: Jan 203113,700 patients
Phase 4Enrolling By Invitation

Acceptability of Human Papillomavirus (HPV) Vaccine in Female Sex Workers

Start: Oct 2009Est. completion: Aug 2011200 patients
Phase 4Completed
NCT06207175Guard TherapeuticsNonavalent HPV study vaccine

A Study to Evaluate the Immunogenicity and Safety of Nonavalent Human Papillomavirus (HPV) Vaccine

Start: Nov 2023Est. completion: Jan 20261,260 patients
Phase 3Unknown
NCT05662020Guard TherapeuticsRecombinant Nonavalent

A Study to Evaluate the Immunogenicity and Safety of HPV Vaccine in Healthy Female Participants Aged 9-26 Years in China

Start: Mar 2022Est. completion: Mar 20282,750 patients
Phase 3Active Not Recruiting
NCT05668572Guard TherapeuticsRecombinant Nonavalent

A Phase III Trial Evaluates the Efficacy, Immunogenicity and Safety Profile of HPV Vaccine

Start: Dec 2020Est. completion: Feb 202312,000 patients
Phase 3Unknown

A Phase III Study of a 2-dose Regimen of a Multivalent Human Papillomavirus (HPV) Vaccine (V503), Administered to 9 to 14 Year-olds and Compared to Young Women, 16 to 26 Years Old (V503-010)

Start: Dec 2013Est. completion: Jul 20171,518 patients
Phase 3Completed

A Study of V503 Given Concomitantly With Menactra™ and Adacel™ in 11 to 15 Year Olds (V503-005)

Start: Oct 2009Est. completion: Feb 20111,241 patients
Phase 3Completed
NCT01095198Merck & Co.offer of vaginal self collection

Randomized Trial of Vaginal Self Sampling for Human Papillomavirus (HPV)

Start: Apr 2010Est. completion: Jan 20131,440 patients
Phase 2/3Unknown

Evaluating Clearance of High-Risk HPV and Safety After Administration of ABI-2280 Vaginal Inserts

Start: Mar 2024Est. completion: Apr 2026141 patients
Phase 1/2Completed
NCT05672966BravoVaxHuman papillomavirus

Phase I Clinical Trial of a Candidate HPV Vaccine

Start: Aug 2023Est. completion: Oct 202440 patients
Phase 1Unknown
NCT05680454Guard TherapeuticsRecombinant Nonavalent

A Phase I Trial Evaluate the Safety and Tolerability Profile of HPV Vaccine

Start: Sep 2019Est. completion: May 2022160 patients
Phase 1Completed

Digital Telecytology for Triage of HPV-Positive Women in Cameroon

Start: Sep 2025Est. completion: Sep 20271,800 patients
N/ARecruiting

Comparative Effectiveness of System Interventions to Increase HPV Vaccine Receipt in FQHCs

Start: May 2018Est. completion: May 202417,000 patients
N/ACompleted
NCT01551537GSKCervarix data collection

Post-marketing Surveillance of GSK Biologicals' Cervarix™ When Administered to Healthy Females in Sri Lanka

Start: Apr 2013Est. completion: Apr 20140
N/AWithdrawn
NCT01205412GSKEndocervical samples

An Observational Study on the Prevalence of Human Papillomavirus Types in Women in the Kingdom of Bahrain

Start: Oct 2010Est. completion: Nov 2011552 patients
N/ACompleted
NCT01158209GSKEndocervical samples

An Observational, Epidemiological Study on the Prevalence of Human Papillomavirus Types in Women in Egypt

Start: Oct 2010Est. completion: Aug 2011490 patients
N/ACompleted
NCT01087164MSDCompliance

Brief Interventions to Increase HPV Vaccine Acceptance in School-based Health Centers

Start: Sep 2010Est. completion: Jun 2014600 patients
N/AUnknown
NCT01702337GSKPrevalence-based model

Prevalence-based Health and Economic Model of the Bivalent Versus the Quadrivalent Human Papillomavirus (HPV) Vaccine

Start: Feb 2010Est. completion: Feb 20101 patients
N/ACompleted
NCT00932009MSDPrevalence and Type Distribution of Human Papillomavirus (HPV) in Tanzanian Men

Prevalence and Type Distribution of Human Papillomavirus (HPV) in Tanzanian Men

Start: Mar 2009Est. completion: Dec 20091,933 patients
N/ACompleted
NCT00572832MSDQuadrivalent human papillomavirus vaccine on-time administration

Randomized Trial of Alternative Quadrivalent Human Papilloma Virus (HPV) Vaccination Schedules in a University Setting

Start: Sep 2007Est. completion: Aug 2009200 patients
N/ACompleted

Phase Legend

Preclinical— Lab & animal studies
Phase 1— Safety & dosing
Phase 2— Efficacy testing
Phase 3— Large-scale trials
On Market— Approved & available

Key Insights

7 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 57,026 patients
10 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.