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NCT06149494
RCT of Vapendavir in Patients With COPD and Human Rhinovirus/Enterovirus Upper Respiratory Infection
Phase 2 trial testing Vapendavir in COPD Exacerbation Acute in 52 participants. Completed in 30 March 2025.
30 March 2025
Quick facts
| Lead sponsor | Altesa Biosciences, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 52 |
| Start date | 20 November 2023 |
| Primary completion | 30 March 2025 |
| Estimated completion | 30 March 2025 |
| Sites | 1 location across United Kingdom |
Drugs / interventions tested
- Vapendavir — full drug profile →
- Placebo
Conditions studied
- COPD Exacerbation Acute — all drugs for COPD Exacerbation Acute →
- COPD With Acute Lower Respiratory Infection — all drugs for COPD With Acute Lower Respiratory Infection →
- Rhinovirus — all drugs for Rhinovirus →
- Virus Diseases — all drugs for Virus Diseases →
Sponsor
Altesa Biosciences, Inc.
Who can join
Adults 40 to 75, any sex, with COPD Exacerbation Acute or COPD With Acute Lower Respiratory Infection. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Vapendavir (VPV) is a drug being developed to treat human rhinovirus (RV) infection, one virus responsible for the common cold. Vapendavir prevents the virus from entering cells and making more infectious copies of itself. A study is being planned to investigate VPV in patients with chronic obstructive pulmonary disease (COPD, a lung disease making it difficult to breathe) who develop a rhinoviral infection; however, VPV has not been approved for use in treating any indication (disease) by the FDA or any other global regulatory agency. Therefore, VPV is considered investigational, and the study doctor is conducting this investigational research study. Safety will be monitored throughout the entire study.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
The common cold: The need for an effective treatment amid the FDA discussion on oral phenylephrine.
Išerić E, Verster JC. · · 2024 · cited 2× · PMID 39253103 · DOI 10.1016/j.jacig.2024.100318 -
A clinical SARS-CoV-2 Mpro inhibitor blocks replication of multiple enteroviruses and confers oral in vivo protection in animal models.
Ye Z, Dai W, Zhang S, Xiang Y, et al · · 2026 · PMID 41811867 · DOI 10.1371/journal.ppat.1014051
Verify or expand the search:
- PubMed search for NCT06149494
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Vapendavir
Trials testing the same drug.
- NCT06834295 — A Study to Evaluate Metabolism, Excretion, and Mass Balance of [14C]Vapendavir · Phase 1, PHASE2 · completed
- NCT05962645 — Phase 1 Study Into Pharmacokinetics and Food Effect of Vapendavir in Healthy Participants and Participants With COPD · Phase 1 · completed
Other recruiting trials for COPD Exacerbation Acute
Currently open trials in the same condition.
- NCT05703919 — Standard vs Targeted Oxygen Therapy Prehospital for Chronic Obstructive Pulmonary Disease · Phase 4 · recruiting
- NCT06274957 — The Effect of Airway and Chest Wall Oscillation on Respiratory Functions in COPD Patients in Acute Exacerbation · NA · recruiting
- NCT06331416 — Multiparametric Home Telemonitoring of Patients With Chronic Obstructive Pulmonary Disease Exacerbation · NA · recruiting
- NCT05452226 — Neuromuscular Electrical Stimulation in COPD/Community Acquired Pneumonia · NA · recruiting
- NCT05568043 — The Reducing REVISITS Study: A Cluster RCT · NA · recruiting
Other Altesa Biosciences, Inc. trials
Trials by the same sponsor.
- NCT06834295 — A Study to Evaluate Metabolism, Excretion, and Mass Balance of [14C]Vapendavir · Phase 1, PHASE2 · completed
- NCT05962645 — Phase 1 Study Into Pharmacokinetics and Food Effect of Vapendavir in Healthy Participants and Participants With COPD · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06149494 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Altesa Biosciences, Inc.
- Last refreshed: 30 September 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06149494.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing