drugset / Trial / NCT05387239
Safety and Effectiveness of VL-PX10 + VL-P22 Treatment on Pulmonary Fibrosis Secondary to Covid-19
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The COVID-induced fibrotic lung damage continues long after viral infection has subsided and is exhibited by severe respiratory pathology and concomitant symptoms. The long-lasting sequelae in patients who have recovered from severe COVID indicate that there is a 30% chance of developing a persistent respiratory system pathology and a 10% chance of developing a severe pathology. The symptoms of lung fibrosis include a severe disruption of respiration, reduction of exercise tolerance, and concomitant development of persistent fibrotic lung damage. This study intends to evaluate benefits of a combination of VL-P22 and VL-PX10 in Covid-19 patients exhibiting pulmonary fibrosis.
Timeline
- Start
- 2022-11-30
- Primary completion
- 2024-11
- Completion
- 2024-12
Outcome
Outcome not reported
Stopped: “Sponsor request”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | VL-P22 | Unknown | — | Intravenous |
| Subject | VL-PX10 | Other / unclassified | — | Intravenous |