drugset / Trial / NCT06216366

Rhu-pGSN to Mitigate Proinflammatory Responses to Decompression in Healthy SCUBA Divers

NCT06216366 ↗

Phase 2 Active not recruiting 36 enrolled BioAegis Therapeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Healthy trained SCUBA divers will be randomized into three groups and exposed to a high-pressure profile in a hyperbaric chamber. The high-pressure profile simulates the pressure at a depth of 30 meters of sea water (MSW) for 35 minutes. In the control group, the subjects will receive intravenous normal saline immediately before and after the high-pressure exposure. The second group will receive intravenous recombinant human gelsolin (rhu-pGSN) 24 mg/kg immediately prior to the exposure, and saline post-exposure. The third group will receive saline pre-exposure and rhu-pGSN post-exposure. Blood samples will be collected at multiple time points pre- and post-exposure to assess levels of inflammatory markers, including interleukin (IL)-1β. Other assessments include screening for gas bubbles, a validated questionnaire to assess the incidence of clinical decompression sickness (DCS), measurement of plasma gelsolin (pGSN) levels, and measurement of anti-pGSN antibodies.

Timeline

Start
2025-08-15
Primary completion
2025-10-30
Completion
2025-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Recombinant human plasma gelsolin Protein / enzyme biologic 24 mg/kg Intravenous