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Review
. 2024;14(s2):S407-S421.
doi: 10.3233/JPD-230354.

Pharmacotherapy for Disease Modification in Early Parkinson's Disease: How Early Should We Be?

Affiliations
Review

Pharmacotherapy for Disease Modification in Early Parkinson's Disease: How Early Should We Be?

Philipp Mahlknecht et al. J Parkinsons Dis. 2024.

Abstract

Slowing or halting progression continues to be a major unmet medical need in Parkinson's disease (PD). Numerous trials over the past decades have tested a broad range of interventions without ultimate success. There are many potential reasons for this failure and much debate has focused on the need to test 'disease-modifying' candidate drugs in the earliest stages of disease. While generally accepted as a rational approach, it is also associated with significant challenges around the selection of trial populations as well as trial outcomes and durations. From a health care perspective, intervening even earlier and before at-risk subjects have gone on to develop overt clinical disease is at the heart of preventive medicine. Recent attempts to develop a framework for a biological definition of PD are aiming to enable 'preclinical' and subtype-specific diagnostic approaches. The present review addresses past efforts towards disease-modification, including drug targets and reasons for failure, as well as novel targets that are currently being explored in disease-modification trials in early established PD. The new biological definitions of PD may offer new opportunities to intervene even earlier. We critically discuss the potential and challenges around planning 'disease-prevention' trials in subjects with biologically defined 'preclinical' or prodromal PD.

Keywords: Parkinson’s disease (PD); biological definition of PD; disease-modification; disease-prevention; neuroprotection; preclinical PD; prodromal PD.

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Conflict of interest statement

P.M. reports lecture fees from AbbVie outside the submitted work. W.P. reports consultancy and lecture fees in relation to clinical drug development programmes for PD from AC Immune, Alterity, AbbVie, Affiris, BIAL, Biogen, Britannia, Lilly, Lundbeck, Merz, Neuroderm, Neurocrine, Roche, Sunovion, Stada, Takeda, UCB and Zambon, all outside the submitted work.

Figures

Fig. 1
Fig. 1
Mechanisms in the pathophysiological cascade of PD and potential treatment targets. See text and Table 3 for more details regarding drug candidates. ASO, antisense oligonucleotide; Cav1.3, Calcium channel, voltage-dependent; GBA, gene encoding for Glucocerebrosidase; GLP-1, Glucagon-like peptide-1; iNOS, Nitric oxide synthases; LRRK2, Leucine rich repeat kinase 2; ROS, reactive oxygen species; siRNA, small interfering RNAs.

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