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NCT06093191: ERASE
Tobramycin Inhalation Solution for Pseudomonas Aeruginosa Eradication in Bronchiectasis
Phase 4 trial testing Tobramycin Inhalant Product in Bronchiectasis Adult in 371 participants. Completed in 15 November 2025.
28 October 2025
Quick facts
| Lead sponsor | Jin-Fu Xu |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 371 |
| Start date | 18 October 2023 |
| Primary completion | 28 October 2025 |
| Estimated completion | 15 November 2025 |
| Sites | 60 locations across China |
Drugs / interventions tested
- Tobramycin Inhalant Product — full drug profile →
- Ciprofloxacin 750 MG — full drug profile →
- Oral ciprofloxacin placebo — full drug profile →
- Natural saline inhalation — full drug profile →
Conditions studied
- Bronchiectasis Adult — all drugs for Bronchiectasis Adult →
- Pseudomonas Aeruginosa Infection — all drugs for Pseudomonas Aeruginosa Infection →
Sponsor
Jin-Fu Xu
Who can join
Adults 18 to 80, any sex, with Bronchiectasis Adult or Pseudomonas Aeruginosa Infection. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
People with bronchiectasis are prone to Pseudomonas aeruginosa (PA) infections, which can become chronic and lead to increased death rates and disease severity. Studies from cystic fibrosis suggest that eradication therapy aimed at PA can successfully transition patients to a culture-negative status, providing long-term benefits. Current guidelines for managing bronchiectasis in adults recommend eradicating PA when it is first or newly isolated; however, there is a lack of randomized controlled trials supporting such recommendations. The researchers hypothesize that both oral ciprofloxacin combined with tobramycin inhalation solution and tobramycin inhalation solution alone are superior to no eradication (inhaled saline) in terms of the eradication rate of PA (with eradication defined as negative sputum culture results on two consecutive occasions separated by an interval of 12 weeks or more after the first drug administration).
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
A phase 4 multicentre, 2×2 factorial randomised, double-blind, placebo-controlled trial to investigate the efficacy and safety of tobramycin inhalation solution for <i>Pseudomonas aeruginosa</i> eradication in bronchiectasis: ERASE.
Gao YH, Lu HW, Zheng HZ, Cao C, et al · · 2024 · cited 7× · PMID 38410702 · DOI 10.1183/23120541.00938-2023 -
Pulmonary Delivery of Antibiotics to the Lungs: Current State and Future Prospects.
Dallal Bashi YH, Mairs R, Murtadha R, Kett V. · · 2025 · cited 6× · PMID 39861758 · DOI 10.3390/pharmaceutics17010111
Verify or expand the search:
- PubMed search for NCT06093191
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Bronchiectasis Adult
Currently open trials in the same condition.
- NCT07289100 — Novel Sensors and Artificial Intelligence for Detection of Acute Pulmonary Exacerbations in Cystic Fibrosis and Bronchie · recruiting
- NCT06900062 — The C-BRIDGE Study: China Bronchiectasis Research Involving Databases, Genomics, and Endotyping · recruiting
- NCT06820918 — Physiotherapy With Positive Expiratory Pressure (PEP) Bottle in Patients With Bronchiectasis · NA · active not recruiting
- NCT06801327 — Comparison Between Conventional Respiratory Physiotherapy and the Simeox Device in Patients With Bronchiectasis · NA · recruiting
- NCT06760273 — Long-term Impact of Inhaled Tobramycin for Pseudomonas Aeruginosa Eradication in Bronchiectasis (ERASE II) · recruiting
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 NCT06093191 (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 Jin-Fu Xu
- Last refreshed: 17 April 2026
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/NCT06093191.
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