Paramyxoviridae Infections clinical trials
The registry lists 31 studies for Paramyxoviridae Infections across 9 countries. 3 are recruiting or about to start. 19 of them are mainly about Paramyxoviridae Infections (how this is decided). Per ClinicalTrials.gov, last updated 2026-11-09. Counting its 3 narrower conditions too, such as Respiratory Syncytial Virus Infections: 478 studies, 69 open.
Get an email when these change. Save the Paramyxoviridae Infections studies recruiting or about to start — once a week, free: studies that open, close, add sites or post results.
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Example · made-up studies
Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
Now Active, not recruiting
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Who runs them
National Institute of Allergy and Infectious Diseases (NIAID) (8) · Ansun Biopharma, Inc. (3) · Biota Pharmaceuticals, Inc. (2) · ModernaTX, Inc. (2) · Assistance Publique - Hôpitaux de Paris (2) · University College, London (1) · DiaSorin Molecular LLC (1) · Clover Biopharmaceuticals AUS Pty (1)
Who develops what
Save this setEvery programme with a company-led study here in the last two years, whatever its size: 8 programmes from 4 companies, 1 with this as their studies’ main aim; 0 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.
| Drug | Leading trial sponsor | Companies, last 5 years |
|---|---|---|
SCB-1019TRecent, limitedEvidence
| — | 11 study |
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 8 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. Phase 4 trial recorded: a phase 4 study exists somewhere; approval here is not checked. Not read yet: approvals and labels, exclusivity, licences, line of therapy, academic comparators, sales.
What is being tested here
Drugs under test in Paramyxoviridae Infections 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 |
|---|---|---|---|
| Oplunofusp | 1 | 1 | 4 |
| Enzaplatovir | 0 | 0 | 3 |
| Interferon beta-1a | 0 | 0 | 1 |
| Interferon Beta-1a Inhalation Solution SNG001 | 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.
The study
- Mar 2027Study of Safety and PK of AZD0543 in Healthy Adults · AstraZeneca
Who these studies take
Of the 3 Paramyxoviridae Infections studies recruiting now, 2 (67%) set no upper age limit and 1 (33%) stop at 75 or younger. 1 (33%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 1 (33%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 1 (33%) | 1 (33%) |
| 18 | 3 (100%) | 3 (100%) |
| 30 | 3 (100%) | 3 (100%) |
| 40 | 3 (100%) | 3 (100%) |
| 50 | 3 (100%) | 3 (100%) |
| 65 | 2 (67%) | 2 (67%) |
| 75 | 2 (67%) | 2 (67%) |
| 85 | 2 (67%) | 2 (67%) |
Across all 31 studies, recruiting or not: 58% stop at 75 or younger and 52% at 65; 48% take children; 0% are for women only and 0% for men only; 58% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
Studies
Recruiting first, then most recently updated. Showing 31 of 31. search them.
- Study of Safety and PK of AZD0543 in Healthy AdultsRecruitingNCT07824622Phase 11 country
- Phase III DAS181 Lower Tract PIV Infection in Immunocompromised Subjects (Substudy: DAS181 for COVID-19): RCT StudyRecruitingNCT03808922Phase 35 countries
- Signature of the Host Response to a Respiratory Viral Infection, in the Prediction of Bronchiolitis ObliteransRecruitingNCT040990821 country
- Safety and Immunogenicity Study of SCB-1022 and SCB-1033 in Healthy Older AdultsActive, not recruitingNCT06984094Phase 1/21 country
- Study of the Infectivity, Safety and Immunogenicity of Two Recombinant, Live-Attenuated, B/HPIV3 Vectored Vaccines Expressing the Fusion Glycoprotein of HMPV Delivered by Nasal Spray to HPIV3-Seropositive Children 24 to <60 Months of AgeCompletedNCT06546423Phase 11 country
- Phase 2 Study of Inhaled SNG001 in Mechanically Ventilated Patients With Respiratory Viral InfectionTerminatedNCT06999603Phase 22 countries
- Study of a Respiratory Syncytial Virus/Human Metapneumovirus/Parainfluenza Virus Type 3 Vaccine Candidate in Adults Aged 60 Years and OlderCompletedNCT06604767Phase 11 country
- A Study to Assess the Safety of Live Intranasal Sendai Virus Vaccine in Children and ToddlersSuspendedNCT00186927Phase 11 country
- A Study on the Safety and Immunogenicity of Influenza, Respiratory Syncytial Virus, Human Metapneumovirus and Parainfluenza Vaccines in Adults 18 to 49 Years of Age.CompletedNCT06850051Phase 11 country
- A Phase 1 Study to Evaluate Safety & Immunogenicity of RVSV-Nipah Virus Vaccine Candidate PHV02 in Healthy Adult SubjectsCompletedNCT05178901Phase 11 country
- Study of ALVR106 in Patients With Respiratory Viral Infections After Hematopoietic Cell and Solid Organ TransplantTerminatedNCT04933968Phase 1/21 country
- LIAISON NES Influenza (FLU) A/B, Respiratory Syncytial Virus (RSV), & Coronavirus Disease 2019 (COVID-19) in Symptomatic Patients in AustraliaStatus unknownNCT06392451Not applicable1 country
- Safety and Immunogenicity of mRNA-1653, a Combined Human Metapneumovirus (hMPV) and Parainfluenza Virus Type 3 (PIV3) Vaccine, in Healthy Adults, and Children 12 to 59 Months of Age With Serologic Evidence of Prior ExposureCompletedNCT04144348Phase 11 country
- Safety, Reactogenicity, and Immunogenicity of mRNA-1653 in Healthy AdultsCompletedNCT03392389Phase 11 country
- DAS181 in Patients With ParainfluenzaWithdrawnNCT01441024Phase 2
- Clinical Features, Outcome and Prognosis of Human Metapneumovirus (hMPV) Lower Respiratory Tract Infections in Adult InpatientsStatus unknownNCT034601711 country
- The Respiratory Protection Effectiveness Clinical TrialCompletedNCT01249625Not applicable1 country
- Safety and Pharmacokinetics Study of Multiple Ascending Doses of BTA-C585 in Healthy VolunteersCompletedNCT02668367Phase 11 country
- Phase 1 Safety and Pharmacokinetics Study of Single Ascending Doses of BTA-C585 in Healthy VolunteersCompletedNCT02558413Phase 11 country
- Safety, Efficacy and Pharmacokinetics of BTA-C585 in a RSV Viral Challenge StudyCompletedNCT02718937Phase 21 country
- A Phase II, Randomized, Double-blind, Placebo-controlled Study to Examine the Effects of DAS181 in Immunocompromised Subjects With Lower Respiratory Tract Parainfluenza Infection on Supplemental OxygenCompletedNCT01644877Phase 21 country
- An Open Label Study to Examine the Effects of DAS181 Administered by Dry Powder Inhaler (DPI) or Nebulized Formulation in Immunocompromised Subjects With Parainfluenza (PIV) InfectionCompletedNCT01924793Phase 21 country
- Collection and Testing of Respiratory SamplesCompletedNCT013024181 country
- Specific Respiratory Infections as Triggers of Acute Medical EventsCompletedNCT029842801 country
- Safety of a Live Attenuated Human Parainfluenza Virus Type 2 (HPIV2) Vaccine for Adults, Children, and InfantsCompletedNCT01139437Phase 11 country
- Evaluating the Safety and Immunogenicity of a Human Parainfluenza Type 3 (HPIV3) Virus Vaccine in Infants and ChildrenCompletedNCT01254175Phase 12 countries
- Safety of and Immune Response to Recombinant Live-Attenuated Parainfluenza Type 1 Virus VaccineCompletedNCT00641017Phase 11 country
- Safety of and Immune Response to Recombinant Live Attenuated Parainfluenza Type 3 Virus Vaccine in Healthy Infants and ChildrenCompletedNCT01021397Phase 11 country
- Safety of and Immune Response to a Cow/Human Parainfluenza Virus Vaccine (rB/HPIV3) in Healthy Infants, Children, and AdultsCompletedNCT00366782Phase 11 country
- Surveillance Study of Viral Infections Following Lung TransplantationCompletedNCT007019221 country
- Safety of and Immune Response to a Human Parainfluenza Virus Vaccine (rHPIV3cp45) in Healthy InfantsCompletedNCT00308412Phase 11 country