HUMAN PAPILLOMAVIRUS, L1 PROTEIN VIRUS LIKE PARTICLES
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Also known as CervarixGardasilGardasil 9Human papillomavirusl1 protein virus like particlesSilgard
Summary
Human Papillomavirus, L1 Protein Virus Like Particles (CHEMBL6068359) is an approved vaccine component; indicated across 2 conditions including human papilloma virus infection.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Vaccine component
- Indications: 2 conditions
- Clinical trials: 67
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL6068359 |
| Name | HUMAN PAPILLOMAVIRUS, L1 PROTEIN VIRUS LIKE PARTICLES |
| Type | Vaccine component |
| Max phase | 4 |
Also known as: Cervarix, Gardasil, Gardasil 9, Human papillomavirus, l1 protein virus like particles, Silgard, HUMAN PAPILLOMAVIRUS, L1 PROTEIN VIRUS LIKE PARTICLES
Targets
Targets
No target linkage available.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| human papilloma virus infection | 4 | MONDO:0005161 | EFO:0001668 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 67.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 17 |
| PHASE3 | 17 |
| Not specified | 14 |
| PHASE2 | 11 |
| PHASE1 | 6 |
| PHASE1/PHASE2 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04206813 | PHASE4 | ACTIVE_NOT_RECRUITING | An Exploratory Open-Label Clinical Trial Evaluating the Immunogenicity of the 9-valent 2-dose HPV Vaccination Regimen |
| NCT06052696 | PHASE4 | NOT_YET_RECRUITING | Adjuvant Nonavalent HPV Vaccination in Women Treated for Vulvar HSIL |
| NCT06536855 | PHASE4 | NOT_YET_RECRUITING | Faster Elimination of HPV Infection and Cervical Cancer Using Concomitant HPV Vaccination and HPV Screening: A Demonstration Project in Rwanda |
| NCT06786429 | PHASE4 | NOT_YET_RECRUITING | Managing Hepatitis B (Hep. B) and Human Papilloma Virus (HPV) Related Cancers and Mental Health. |
| NCT07314307 | PHASE4 | ACTIVE_NOT_RECRUITING | Vaccine Effectiveness of One Dose of the Nonavalent Human Papillomavirus (HPV) Vaccine Among Young-adult Women in Sweden Among Women Participating in a Clinical Trial of Concomitant HPV Vaccination and Screening |
| NCT00534638 | PHASE4 | COMPLETED | Effectiveness, Safety and Immunogenicity of GSK Biologicals’ HPV Vaccine GSK580299 (Cervarix) Administered in Healthy Adolescents |
| NCT00730847 | PHASE4 | TERMINATED | A Study to Assess the Safety and Reactogenicity of GlaxoSmithKline (GSK) Biologicals’ Human Papillomavirus (HPV) Vaccine (Cervarix) in Healthy Female Filipino Subjects Vaccinated According to the Prescribing Information From the Age of 10 Years Onwards. |
| NCT00925288 | PHASE4 | COMPLETED | Acceptability of Human Papillomavirus (HPV) Vaccine in Female Sex Workers |
| NCT00956553 | PHASE4 | COMPLETED | Reactogenicity Study of Cervarix and Gardasil in UK Adolescent Girls |
| NCT01082861 | PHASE4 | TERMINATED | Efficacy and Immunomodulation Study of Simultaneous Human Papillomavirus/ Hepatitis B (HPV/HBV) Vaccination |
| NCT01386164 | PHASE4 | COMPLETED | Immune Response to Bivalent and Tetravalent Human Papillomavirus Vaccine in HIV Infected Adults |
| NCT01824537 | PHASE4 | COMPLETED | Transmission Reduction and Prevention With HPV Vaccination (TRAP-HPV) Study |
| NCT01914367 | PHASE4 | COMPLETED | Study of the Molecular Mechanisms Underlying the Cross-neutralizing Capacity of AS04-adjuvanted HPV Vaccine (Cervarix®) in Comparison With the Aluminiumhydroxyphosphate Sulphate Adjuvanted HPV Vaccine (Gardasil®) |
| NCT02087384 | PHASE4 | COMPLETED | HPV (Human Papilloma Virus) Vaccination After Treatment of Anal Intraepithelial Neoplasia (AIN) |
| NCT02837926 | PHASE4 | COMPLETED | Comparing Health Services Interventions for the Prevention of HPV-related Cancer |
| NCT03105856 | PHASE4 | COMPLETED | FASTER-Tlalpan Study in Mexico: HPV Vaccination Impact on Cervical Cancer Screening Program |
| NCT04459221 | PHASE4 | COMPLETED | Study of the Impact of a School Program Combining - Promotion of HPV Vaccination and HPV Vaccine Offer in Middle School - on Adherence to HPV Vaccination in Middle School Students |
| NCT03998254 | PHASE3 | ACTIVE_NOT_RECRUITING | Efficacy, Immunogenicity and Safety of V503 in Chinese Women Aged 20-45 Years (V503-023) |
| NCT00092495 | PHASE3 | COMPLETED | Study of an Investigational Vaccine in Pre-Adolescents and Adolescents (Gardasil)(V501-016) |
| NCT00092534 | PHASE3 | COMPLETED | Cervical Intraepithelial Neoplasm (CIN) in Women (Gardasil) (V501-015) |
| NCT00196937 | PHASE3 | COMPLETED | Human Papilloma Virus (HPV) Vaccine Immunogenicity and Safety Trial in Young and Adult Women With GSK Biologicals’ HPV-16/18 |
| NCT00294047 | PHASE3 | COMPLETED | Study to Evaluate the Efficacy of the Human Papillomavirus Vaccine in Healthy Adult Women of 26 Years of Age and Older |
| NCT00481767 | PHASE3 | COMPLETED | Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals’ Human Papillomavirus (HPV) Vaccine (GSK580299) in Healthy Female Subjects 10-25 Years of Age. |
| NCT00543543 | PHASE3 | COMPLETED | Broad Spectrum HPV (Human Papillomavirus) Vaccine Study in 16-to 26-Year-Old Women (V503-001) |
| NCT00811798 | PHASE3 | COMPLETED | Safety Study of GSK Biologicals’ HPV Vaccine (GSK-580299) in Healthy Female Subjects. |
| NCT00964210 | PHASE3 | COMPLETED | Protecting Young Special Risk Females From Cervical Cancer Through Human Papilloma Virus (HPV) Vaccination |
| NCT01190176 | PHASE3 | COMPLETED | Gynaecological Follow-up of a Subset of HPV-015 (NCT00294047) Study Subjects |
| NCT01304498 | PHASE3 | COMPLETED | Immunogenicity and Tolerability of V503 Versus GARDASIL (V503-009) |
| NCT01375868 | PHASE3 | COMPLETED | Effect of Vaccination in Patients With Recurrent Respiratory Papillomatosis |
| NCT01462357 | PHASE3 | COMPLETED | Immunogenicity and Safety Study of GlaxoSmithKline Biologicals’ Human Papillomavirus (HPV) Vaccine (GSK-580299) and Merck’s Gardasil Vaccine When Administered According to Alternative 2-dose Schedules in 9-14 Year Old Females |
| NCT01627561 | PHASE3 | COMPLETED | Safety and Immunogenicity of GSK Biologicals’ HPV-16/18 L1 VLP AS04 Vaccine (GSK-580299) in Healthy Female Children 4-6 Years Old |
| NCT02114385 | PHASE3 | COMPLETED | A Study to Compare Immune Response of V503 to Gardasil in 16- to 26-year-old Men (V503-020) |
| NCT03431246 | PHASE3 | COMPLETED | Immunogenicity of One Dose of Gardasil and One Dose of Gardasil-9 |
| NCT05580341 | PHASE3 | UNKNOWN | Phase III Study Comparing the Immunogenicity of 9-valent HPV Recombinant Vaccine and Gardasil-9 |
| NCT03519464 | PHASE2 | ACTIVE_NOT_RECRUITING | Immunogenicity of the 9-Valent Human Papillomavirus Recombinant Vaccine in People With Idiopathic CD4 T Cell Lymphocytopenia |
| NCT07407569 | PHASE2 | RECRUITING | Developing a First-void Urine-based Infection Model to Study HPV-specific Antibody-virion Interaction Before and After HPV Vaccination |
| NCT00260039 | PHASE2 | COMPLETED | Broad Spectrum HPV Vaccine Dose Ranging Study (V502-001) |
| NCT00309166 | PHASE2 | COMPLETED | Evaluation of the Immunogenicity and Safety of GlaxoSmithKline Biologicals’ HPV Vaccine in Young Males. |
| NCT00513526 | PHASE2 | COMPLETED | Human Papillomavirus Vaccine Therapy in Treating Men With HIV-1 Infection |
| NCT00518336 | PHASE2 | COMPLETED | Follow-up Study to Evaluate the Long-term Efficacy of the HPV Vaccine (580299) in Healthy Young Adult Women in Brazil |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: human papilloma virus infection