Hand, Foot and Mouth Disease clinical trials
The registry lists 59 studies for Hand, Foot and Mouth Disease across more than 10 countries. 10 are recruiting or about to start. 55 of them are mainly about Hand, Foot and Mouth Disease (how this is decided). Per ClinicalTrials.gov, last updated 2026-10-13.
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Status
Who runs them
Sinovac Biotech Co., Ltd (20) · Jiangsu Province Centers for Disease Control and Prevention (7) · Institute of Medical Biology, Chinese Academy of Medical Sciences (7) · Enimmune Corporation (3) · Oxford University Clinical Research Unit, Vietnam (2) · HK inno.N Corporation (2) · Chinese Academy of Medical Sciences (2) · The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine (2)
Who develops what
Save this setEvery programme with a company-led study here in the last two years, whatever its size: 5 programmes from 1 company, 5 with this as their studies’ main aim; 3 with a live phase 3 study; 0 primary completions in the next 12 months.
Comparator & background therapies
What other companies’ phase 2+ studies give as the comparator or the background here (its leading trial sponsor and partners left out): a sign of what new drugs are measured against, not by itself the standard of care, its prescriptions or its market.
None given by two companies or more yet.
Programmes
“Meets, by arms” reads each study’s arms: vs its arm against the therapy’s; + X vs a combination against it; added to it plus the therapy against the therapy; studied with given together only. The next primary completion is the next phase-3 study’s when there is one.
The 5 programmes — sign in to see the whole list, free: filter by phase and aim, sort by late development, direct comparisons or the next primary completion.
Primary completion in the next 12 months (0)
Live phase 2 and 3 studies of these programmes. Primary completion is when the main measure’s data collection ends, as the registry states it (most are estimates); results come later, if they are announced.
None in the next 12 months.
Read from ClinicalTrials.gov, industry-led studies. Main aim: this is the study’s judged main condition; named, not the main aim: the sponsor names it, the study is about something else; registry mapping only: only the registry’s mapping put it here. Leading trial sponsor is the company leading the most industry studies of a drug, a measure of trial activity, not of rights. US and EU rights, and Approved: from the regulators’ records (FDA’s Drugs@FDA via openFDA; EMA’s medicines data) — the holder of a marketed or authorised original, generics and other companies’ versions; not rights elsewhere, nor approval for this condition. Phase 4 trial recorded, where neither lists it: a phase 4 study exists somewhere. Not read yet: labels by indication, exclusivity, licences, line of therapy, academic comparators, sales.
What is being tested here
Drugs under test in Hand, Foot and Mouth Disease studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
| Drug | Open | Phase 3 | All |
|---|---|---|---|
| Enterovirus 71 vaccine | 2 | 2 | 7 |
| EV71 | 0 | 0 | 4 |
| Sucralfate | 0 | 0 | 1 |
| Magnesium Sulfate | 0 | 0 | 1 |
| Suramin | 0 | 0 | 1 |
| Andrographolide sulfonate | 0 | 0 | 1 |
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 2
- Jan 2027Bridging Clinical Trial of EV71 Vaccine in Vietnamese Children · Sinovac Biotech Co., Ltd
- Mar 2027CHIPCAT and HFMD-PREP for HFMD Prevention in Childcare Centres in Kota Kinabalu · Helmy Sajali, MD, MPH
Who these studies take
Of the 4 Hand, Foot and Mouth Disease studies recruiting now, 1 (25%) set no upper age limit and 3 (75%) stop at 75 or younger. 4 (100%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 3 (75%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 2 (50%) | 2 (50%) |
| 18 | 1 (25%) | 1 (25%) |
| 30 | 1 (25%) | 1 (25%) |
| 40 | 1 (25%) | 1 (25%) |
| 50 | 1 (25%) | 1 (25%) |
| 65 | 1 (25%) | 1 (25%) |
| 75 | 1 (25%) | 1 (25%) |
| 85 | 1 (25%) | 1 (25%) |
Across all 59 studies, recruiting or not: 93% stop at 75 or younger and 93% at 65; 92% take children; 0% are for women only and 0% for men only; 73% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
Studies
Recruiting first, then most recently updated. Showing 50 of 59. Browse all 59 → or search them.
- CHIPCAT and HFMD-PREP for HFMD Prevention in Childcare Centres in Kota KinabaluNot yet recruitingNCT07839442Not applicable1 country
- Bridging Clinical Trial of EV71 Vaccine in Vietnamese ChildrenNot yet recruitingNCT07793175Not applicable1 country
- Protective Efficacy , Immunogenicity and Safety of the Tetravalent Inactivated Enterovirus Vaccine (Vero Cell).Not yet recruitingNCT07611513Phase 31 country
- Phase I Clinical Trial of Enterovirus Type71 - Coxsackievirus Type A16 Bivalent VaccineNot yet recruitingNCT07326878Phase 11 country
- Study on the Persistence of Immunity Following EV71 VaccinationEnrolling by invitationNCT071442021 country
- Efficacy, Safety, and Immunogenicity of the Bivalent Inactivated Enterovirus Vaccine (Vero Cell)RecruitingNCT06734832Phase 31 country
- Artificial Intelligence-driven Virtual Standardized Pediatric Patients TrialRecruitingNCT06699433Not applicable1 country
- Surveillance of HFMD in Pediatric OutpatientsRecruitingNCT062634391 country
- Active Case Finding of Clinical Hand Foot Mouth Disease in Children Aged 6 Months Old to 18 Years Old in IndonesiaNot yet recruitingNCT06251219
- Lot-to-lot Consistency Study of Three Commercial Batches of Enterovirus 71 VaccineRecruitingNCT06146088Phase 41 country
- A Study to Evaluate the Efficacy, Immunogenicity and Safety of an EV71 Vaccine in Healthy Infants and ChildrenCompletedNCT05099029Phase 32 countries
- Inactivated Bivalent Enterovirus Vaccine (Vero Cell) Phase I/II Clinical TrialCompletedNCT06063057Phase 1/21 country
- Tolerability, Safety, and Immunogenicity of Tetravalent Inactivated Enterovirus Vaccine (Vero Cell).CompletedNCT06754384Phase 1/21 country
- Hand, Foot, and Mouth Disease: Could EPs®7630 be a Treatment OptionCompletedNCT06353477Phase 2/31 country
- Immunogenicity of the Inactivated EV71 Vaccine Combined With Hepatitis B and Group A Meningococcal VaccineActive, not recruitingNCT06209398Phase 41 country
- A Serosurvey Study of Hand, Foot, and Mouth Disease in IndonesiaCompletedNCT056372291 country
- A Safety Study of Inactivated EV71 Vaccine (Human Diploid Cell, KMB-17) in Chinese Adults, Children and InfantsCompletedNCT01391494Phase 11 country
- A Protected Study of Inactivated EV71 Vaccine (Human Diploid Cell, KMB-17) in Chinese Infants and ChildrenCompletedNCT01569581Phase 31 country
- A Phase II, Safety and Efficacy Study of Inactivated EV 71 Vaccine (Human Diploid Cell, KMB-17) in Chinese InfantsCompletedNCT01512706Phase 21 country
- The Phase IVb of Inactivated Enterovirus 71 Vaccine (Human Diploid Cell, KMB-17) in Chinese ChildrenCompletedNCT03001986Phase 41 country
- The Immunogenicity and Safety of the Vaccination of Inactivated Enterovirus 71 Vaccine and Seasonal Influenza VaccineCompletedNCT04133584Phase 41 country
- Safety Observation of Enterovirus 71 Inactivated Vaccine (Vero Cell) Combined Immunization in ShanghaiStatus unknownNCT051660441 country
- An Immunity Persistence Study of Enterovirus 71 Inactivated Vaccine (Vero Cell)Status unknownNCT05397587Phase 41 country
- A Follow-up Study for a Phase III, Efficacy Trial in Inactivated Enterovirus Type 71 (EV71) VaccineCompletedNCT020012331 country
- Clinical Trial of Enterovirus 71(EV71) Inactivated Vaccine in Children Aged 36-71 MonthsCompletedNCT03909074Phase 31 country
- Sucralfate to Improve Oral Intake in Children With Infectious Oral Ulcers: a Randomized, Double-blind, Placebo-Controlled TrialCompletedNCT03241030Phase 21 country
- A Study to Evaluate the Immunogenicity and Safety of EV71 Vaccine in Pediatric SubjectsCompletedNCT03268083Phase 21 country
- Immunogenicity and Safety of Two Different Commercial EV71 VaccinesCompletedNCT03873740Phase 41 country
- Safety and Immunogenicity of Concomitant Administration of EV71 Vaccine With EPI VaccinesCompletedNCT03274102Phase 41 country
- Safety and Immunogenicity of Concomitant Administration of EV71 Vaccine With Expanded Programme on Immunization VaccinesCompletedNCT04111432Phase 41 country
- Safety of an Inactivated Enterovirus Type 71 Vaccines in Healthy ChildrenCompletedNCT01273246Phase 11 country
- Efficacy Trial of a Commercial EV71 VaccineCompletedNCT03903926Phase 41 country
- Immunity and Safety of Inactivated Enterovirus 71 Vaccine Post-marketing Among Children Aged 6-35 Months in ChinaCompletedNCT03893747Phase 41 country
- Efficacy Evaluation for Inactivated Vaccine (Vero Cell) Against EV71CompletedNCT03582761Phase 41 country
- Safety & Immunogenicity of Enterovirus Type 71 Vaccine in Healthy Adults and Children 6-71monthsCompletedNCT04467541Phase 1/21 country
- Safety and Immunogenicity of High-dose IN-B001 in Healthy SubjectsStatus unknownNCT04637919Phase 11 country
- Safety and Immunogenicity of CJ-40010 in Healthy SubjectsStatus unknownNCT04182932Phase 11 country
- Study to Evaluate the Tolerance and Pharmacokinetics of Suramin SodiumStatus unknownNCT03804749Phase 11 country
- Phase IV Clinical Trial, Immunogenicity and Safety of EV71 VaccineCompletedNCT03278132Phase 41 country
- The Phase IVd of Inactivated Enterovirus 71 VaccineStatus unknownNCT03296410Phase 41 country
- Five-year Immune Persistence Study of Inactivated Enterovirus Type 71 (EV71) VaccineCompletedNCT032811741 country
- The Phase IVc of Inactivated Enterovirus 71 Vaccine (Human Diploid Cell)Status unknownNCT03240744Phase 41 country
- Magnesium Sulphate for Severe Hand, Foot and Mouth Disease in VietnamCompletedNCT01940250Phase 21 country
- A Study to Evaluate the Safety and Immunogenicity of EV71 Vaccine in Pediatric Subjects Aged 3 to 6 Years and 6 to 35 Months OldCompletedNCT02777411Phase 21 country
- Neurodevelopment Outcomes Following Severe Hand Foot and Mouth Disease in VietnamCompletedNCT020667141 country
- Safety, Three Batches Consistency and Immunity Duration of the Post-marketing Inactivated Enterovirus Type 71 (EV71) Vaccine in Children Aged 6-71 MonthsStatus unknownNCT02889497Phase 4
- Safety and Immunogenicity Study of an Inactivated Vaccine Against Hand, Foot and Mouth Disease Caused by Enterovirus 71CompletedNCT01376479Phase 11 country
- An Efficacy Trial in Inactivated Enterovirus Type 71 (EV71) VaccineCompletedNCT01507857Phase 31 country
- A Clinical Trial to Assess the Efficacy and Safety of an Inactivated Vaccine (Vero Cell) Against EV71 in Chinese Children Aged 6-35 MonthsCompletedNCT01508247Phase 31 country
- Immunogenicity and Safety of Three Consecutive Lots of a New Inactivated Enterovirus Type 71 (EV71) VaccineCompletedNCT01636245Phase 31 country