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NCT06177249: rabies
To Evaluate the Immunogenicity and Safety of Two Different Immunization Schedules of Rabies Vaccine (Vero Cell)
Phase 3 trial testing Control vaccine in Rabies Human in 1,956 participants. Completed in 1 May 2016.
16 December 2015
Quick facts
| Lead sponsor | Hualan Biological Bacterin Co. Ltd. |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | health services research |
| Enrollment | 1,956 |
| Start date | 15 March 2015 |
| Primary completion | 16 December 2015 |
| Estimated completion | 1 May 2016 |
| Sites | 1 location across China |
Drugs / interventions tested
- Control vaccine — full drug profile →
- Experimental vaccine — full drug profile →
Conditions studied
- Rabies Human — all drugs for Rabies Human →
Sponsor
Hualan Biological Bacterin Co. Ltd. — full company profile →
Who can join
Adults 9 to 65, any sex, with Rabies Human. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To evaluate the safety and immunogenicity of lyophilized human rabies vaccine (Vero cell) developed by Hualan Biological in healthy people aged 9 to 65 years with two different immunization schedules.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06177249
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Control vaccine
Trials testing the same drug.
- NCT05960097 — A Study on the Safety and Immune Response of Investigational COVID-19 mRNA Vaccines in Healthy Adults · Phase 2 · completed
Other Hualan Biological Bacterin Co. Ltd. trials
Trials by the same sponsor.
- NCT06334510 — Evaluate the Safety and Efficacy of Quadrivalent Influenza in Real-world Situations. · completed
- NCT06095947 — Exploration on the Quadrivalent Influenza Vaccine Immunization Schedule for Children Aged 3-8 Years · completed
- NCT03196661 — Preliminary Study on Safety and Immunogenicity of Influenza A (H7N9) Vaccine in the Population · 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 NCT06177249 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hualan Biological Bacterin Co. Ltd.
- Last refreshed: 20 December 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/NCT06177249.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing