Trials / Not Yet Recruiting
Not Yet RecruitingNCT06756191
Antifungal Drugs in Pulmonary Mucormycosis
Evaluation on Efficacy and Safety of Liposomal Amphotericin B(AmBisome® ) Combination with Isavuconazole Versus AmBisome® Alone for Treatment of Patients with Pulmonary Mucormycosis
- Status
- Not Yet Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 312 (estimated)
- Sponsor
- Bin Cao · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Pulmonary mucormycosis (PM) poses a substantial clinical challenge, particularly among immunocompromised patients. The aim of the study is to determine the effectiveness and safety of administering AmBisome at a dose of 5mg/kg/day combined with isavuconazole versus using AmBisome for the management of pulmonary mucormycosis
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Combination therapy group | Liposomal amphotericin B (AmBisome®) combination with Isavuconazole |
| DRUG | Liposomal Amphotericin B | Liposomal amphotericin B (AmBisome®) alone |
Timeline
- Start date
- 2025-01-10
- Primary completion
- 2025-07-10
- Completion
- 2026-12-31
- First posted
- 2025-01-01
- Last updated
- 2025-01-01
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06756191. Inclusion in this directory is not an endorsement.