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NCT04926506
Efficacy and Safety of Intramuscular Injection of Xiyanping Injection in the Treatment of Acute Bronchitis in Children
NA trial testing Xiyanping injection in Acute Bronchitis in Children in 80 participants. Status unknown.
21 September 2022
Quick facts
| Lead sponsor | Jiangxi Qingfeng Pharmaceutical Co. Ltd. |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 80 |
| Start date | 8 October 2021 |
| Primary completion | 21 September 2022 |
| Estimated completion | 30 December 2022 |
Drugs / interventions tested
- Xiyanping injection — full drug profile →
Conditions studied
- Acute Bronchitis in Children — all drugs for Acute Bronchitis in Children →
Sponsor
Jiangxi Qingfeng Pharmaceutical Co. Ltd. — full company profile →
Who can join
Adults 1 to 6, any sex, with Acute Bronchitis in Children. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Any pathogen that causes an upper respiratory tract infection can cause bronchitis.The primary pathogen is virus. On the basis of virus infection, pathogenic bacteria may cause secondary infection or co-infection。Xiyanping injection is mainly used in the treatment of bronchitis by intravenous injection。
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04926506
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Xiyanping injection
Trials testing the same drug.
- NCT04275388 — Xiyanping Injection for the Treatment of New Coronavirus Infected Pneumonia · unknown
Other Jiangxi Qingfeng Pharmaceutical Co. Ltd. trials
Trials by the same sponsor.
- NCT06574503 — Study to Assess the Efficacy and Safety of GP681 Versus Placebo for Postexposure Prophylaxis Against Influenza · Phase 3 · recruiting
- NCT06573008 — Study of GP681 Tablets Compared With Placebo in Patients With Influenza at High Risk of Influenza Complications · Phase 3 · recruiting
- NCT06678542 — Study to Assess Relative Bioavailability of GP681 Formulations in Healthy Chinese Male Subjects · Phase 1 · completed
- NCT06643156 — Study to Assess the Tolerability, Safety and Efficacy of GP681 Powder for Oral Suspension · Phase 1 · completed
- NCT05814926 — GP681 in Volunteers With Hepatic Impairment Compared With Healthy Volunteers · 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 NCT04926506 (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 Jiangxi Qingfeng Pharmaceutical Co. Ltd.
- Last refreshed: 4 October 2021
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/NCT04926506.
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