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NCT05083039
Observational Program, Study the Preventive Efficacy of the BiVac Polio Vaccine Against the Incidence of Acute Respiratory Infections, Including COVID-19
trial in Coronavirus Infections in 1,500 participants. Completed in 3 September 2021.
14 December 2020
Quick facts
| Lead sponsor | Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 1,500 |
| Start date | 14 May 2020 |
| Primary completion | 14 December 2020 |
| Estimated completion | 3 September 2021 |
| Sites | 1 location across Russia |
Conditions studied
- Coronavirus Infections — all drugs for Coronavirus Infections →
- Vaccine — all drugs for Vaccine →
- Polio — all drugs for Polio →
Sponsor
Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products — full company profile →
Who can join
Adults 18 to 65, any sex, with Coronavirus Infections or Vaccine. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Observational program, double-blind, placebo-controlled to study the preventive efficacy of the BiVac polio (Oral polio vaccine, divalent, live attenuated of types 1 and 3 vaccine against the incidence of acute respiratory infections, including COVID-19
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Vaccination With Oral Polio Vaccine Reduces COVID-19 Incidence.
Yagovkina NV, Zheleznov LM, Subbotina KA, Tsaan AA, et al · · 2022 · cited 25× · PMID 35711442 · DOI 10.3389/fimmu.2022.907341
Verify or expand the search:
- PubMed search for NCT05083039
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products trials
Trials by the same sponsor.
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- NCT05765773 — An Open Comparative Study of the Effectiveness and Incomparable Study of the Immunogenicity and Safety of the Vaccine (C · Phase 2 · completed
- NCT05046548 — This is a Double-blind, Placebo-controlled, Randomized Study of the Tolerability, Safety and Immunogenicity of an Inacti · Phase 1, PHASE2 · 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 NCT05083039 (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 Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products
- Last refreshed: 8 February 2023
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/NCT05083039.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing