A Study to Assess the Safety and Efficacy of Centhaquine in Hypovolemic Shock Patients
StatusRecruiting
PhasePhase 4
Started2021-08-13
View on ClinicalTrials.gov ↗
Record status
This record was last updated December 31, 2025 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.
This is a prospective, multi-centric, open-labeled, phase-IV clinical study to evaluate the safety and efficacy of centhaquine citrate (LYFAQUIN™), a first-in-class drug for treating hypovolemic shock, a life-threatening condition caused by severe blood or fluid loss. Centhaquine has been found to be an effective resuscitative agent in rat, rabbit, and swine models of hemorrhagic shock. It has demonstrated the ability to decrease blood lactate levels, increase mean arterial pressure, enhance cardiac output, and reduce mortality rates. The increase in cardiac output during resuscitation is primarily attributed to an augmentation in stroke volume. Centhaquine exerts its effects by acting on the venous α2B-adrenergic receptors, which enhances venous return to the heart. Additionally, it produces arterial dilation by targeting central α2A-adrenergic receptors, thereby reducing sympathetic activity and systemic vascular resistance.
Amendment record
Amended 2 times since 2023-07-13; most recent filed 2025-12-26. Every amendment is listed below.
Dates here are the day the sponsor filed the amendment, not the day ClinicalTrials.gov published it. Version history last read from ClinicalTrials.gov on 2026-08-31.
2025-12-26
Amendment Study Status, Oversight v2
2025-05-09
Amendment Study Status, Oversight, References v1
2023-07-13
Original filing
| NCT Number |
NCT05956418 |
| Lead Sponsor |
Pharmazz, Inc.
|
| Conditions |
Hypovolemic Shock |
| Enrollment |
400 participants |
| Start Date |
2021-08-13 |
| Primary Completion |
2026-06 (estimated) |
| Study Completion |
2026-08 (estimated) |
| Updated on ClinicalTrials.gov |
2025-12-31 |