# Protocol of ASPro-PD: a phase 3 trial of ambroxol to slow progression in genetically stratified Parkinson’s disease

**Authors:** Marco Toffoli, Elisa Menozzi, Mairead Cullen, Kashfia Chowdhury, Saiam Ahmed, Nick Freemantle, Joy Duffen, Richard K. Wyse, Simon R. W. Stott, Helen Matthews, David Dexter, Felicia Ikeji, Julie Moss, Paul Watts, Tom Foltynie, Karl Kieburtz, Olivier Rascol, Werner Poewe, Anthony H. V. Schapira

PMC · DOI: 10.1007/s00415-026-13683-7 · Journal of Neurology · 2026-02-18

## TL;DR

This study tests if ambroxol can slow Parkinson's disease progression in patients with a specific genetic risk factor.

## Contribution

The trial is the largest to study ambroxol in genetically stratified Parkinson’s disease patients.

## Key findings

- The trial will assess ambroxol's effect on motor and non-motor Parkinson’s disease symptoms.
- It will use biomarkers to explore ambroxol’s impact on GCase activity and disease progression.
- The study includes a genetically defined patient population for more targeted insights.

## Abstract

Genetic studies have identified the GBA1 gene as a significant genetic risk factor for Parkinson’s disease (PD), with 10–15% of PD patients carrying GBA1 variants. GBA1 variants affect the glucocerebrosidase (GCase) enzyme, often leading to reduced GCase activity and associated altered lysosomal function, implicated in PD pathogenesis. Ambroxol, a small molecule widely used for respiratory diseases, has emerged as a potential therapeutic agent for PD, acting by increasing GCase activity. A phase 2 trial demonstrated ambroxol’s safety and efficacy in penetrating cerebrospinal fluid (CSF) and engaging with its target in PD patients, including those with GBA1 variants.

We present the protocol of the ASPro-PD trial, a phase 3, multicentre, randomised, double-blind, placebo-controlled trial, aimed at evaluating whether high-dose ambroxol improves motor and non-motor function in PD patients. The trial will enrol 330 PD patients with confirmed GBA1 status and the primary outcome will be the combined score of parts I, II, and III of the Movement Disorders Society–Unified Parkinson’s Disease Rating Scale (MDS-UPDRS). The secondary outcomes include safety, impact on PD symptoms, and quality of life. Mechanistic and exploratory outcomes include biomarkers related to GCase activity, blood, and CSF biomarkers.

This trial is the largest to date to study the effect of ambroxol in PD, utilise a genetically stratified PD population and will provide robust estimates of the efficacy of ambroxol in slowing PD clinical progression.

The online version contains supplementary material available at 10.1007/s00415-026-13683-7.

## Linked entities

- **Genes:** GBA1 (glucosylceramidase beta 1) [NCBI Gene 2629]
- **Proteins:** Gba1 (glucosylceramidase beta 1)
- **Chemicals:** ambroxol (PubChem CID 2132)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, GBA1 (glucosylceramidase beta 1) [NCBI Gene 2629] {aka GBA, GCB, GLUC}, LRRK2 (leucine rich repeat kinase 2) [NCBI Gene 120892] {aka AURA17, DARDARIN, PARK8, RIPK7, ROCO2}
- **Diseases:** vomiting (MESH:D014839), anaphylactic (MESH:D000707), rash (MESH:D005076), urticaria (MESH:D014581), Dresden Falls (MESH:C537863), nausea (MESH:D009325), GD (MESH:D005776), diarrhoea (MESH:D003967), Alzheimer's disease (MESH:D000544), abdominal pain (MESH:D015746), lysosomal storage disorder (MESH:D016464), DLB (MESH:D020961), neurodegeneration (MESH:D019636), respiratory diseases (MESH:D012140), PD (MESH:D010300), dyspepsia (MESH:D004415), Movement Disorders (MESH:D009069), dry mouth (MESH:D014987), Depression (MESH:D003866), dyskinesia (MESH:D004409), Parkinson (MESH:D010302), Dementia (MESH:D003704), coagulation (MESH:D001778), numbness in throat and mouth (MESH:D006987)
- **Chemicals:** glucosylceramide (MESH:D005963), Exenatide (MESH:D000077270), IMP (MESH:D007291), Ambroxol (MESH:D000551), dopamine (MESH:D004298), lipid (MESH:D008055), ASPro-PD (-), levodopa (MESH:D007980)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** N370S

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916515/full.md

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Source: https://tomesphere.com/paper/PMC12916515