# Safety, Efficacy, & PK of PRX-102 in Patients With Fabry Disease Administered Intravenously Every 4 Weeks

> **NCT03180840** · PHASE3 · COMPLETED · sponsor: **Protalix** · enrollment: 30 (actual)

## Conditions studied

- Fabry Disease

## Interventions

- **BIOLOGICAL:** Pegunigalsidase alfa

## Key facts

- **NCT ID:** NCT03180840
- **Lead sponsor:** Protalix
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2017-07-10
- **Primary completion:** 2020-08-01
- **Final completion:** 2020-08-01
- **Target enrollment:** 30 (ACTUAL)
- **Last updated:** 2023-09-13

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03180840

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03180840, "Safety, Efficacy, & PK of PRX-102 in Patients With Fabry Disease Administered Intravenously Every 4 Weeks". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT03180840. Licensed CC0.

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