# Advanced Therapeutics in Parkinson’s Disease: What’s New?

**Authors:** Mariana H.G. Monje, Jessica A. Karl, Christa S. Cooper, Jacob Yomtoob, Juan Deliz, Lucy A. Morse, Neil Shetty, Leonard Verhagen Metman

PMC · DOI: 10.1007/s11910-026-01483-5 · Current Neurology and Neuroscience Reports · 2026-02-18

## TL;DR

This paper reviews recent advances in Parkinson’s disease therapies, including new drug delivery methods, improved deep brain stimulation, and emerging cell-based treatments.

## Contribution

The paper provides a clinically oriented update on novel and improved therapeutic approaches for Parkinson’s disease.

## Key findings

- Subcutaneous infusion therapies reduce OFF time and improve motor function in Parkinson’s patients.
- Adaptive deep brain stimulation using local field potentials may enhance symptom control with lower energy use.
- Magnetic resonance guided focused ultrasound and stem cell-derived grafts show promise as emerging therapies.

## Abstract

To provide a concise, clinically oriented update on advanced therapies for Parkinson’s disease.

Subcutaneous infusion of foscarbidopa/foslevodopa and apomorphine reduce OFF time and improve “good ON time”, though infusion site reactions remain of some concern. Image-guided programming may shorten programming time while matching motor outcomes; while adaptive/closed-loop deep brain stimulation using local field potential signals may improve symptoms and quality of life with a lower energy use. Remote programming accelerates clinical benefit and expands access. Approved magnetic resonance guided high intensity focused ultrasound targets now include the ventralis intermediate nucleus of the thalamus, the globus pallidus pars interna and, recently, the pallidothalamic tract; while research investigates the subthalamic nucleus, each target with distinct benefits and adverse event profiles. Early studies using magnetic resonance guided low intensity focused ultrasound show safe, transient blood brain barrier opening. First-in-human stem cells-derived dopaminergic grafts show safety and graft functioning.

The advanced therapeutic landscape for Parkinson’s disease has evolved through innovations in established and novel therapies. Future priorities for the field include standardized biomarkers and protocols for adaptive deep brain stimulation, long-term evaluation of high intensity focused ultrasound outcomes, and rigorously controlled trials of low intensity focused ultrasound and cell-based therapies designed to assess disease-modifying potential.

## Linked entities

- **Chemicals:** foscarbidopa (PubChem CID 121288738), foslevodopa (PubChem CID 127766), apomorphine (PubChem CID 2215)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** VIM (vimentin) [NCBI Gene 7431], GBA1 (glucosylceramidase beta 1) [NCBI Gene 2629] {aka GBA, GCB, GLUC}
- **Diseases:** AEs (MESH:D064420), anxiety (MESH:D001007), essential tremor (MESH:D020329), edema (MESH:D004487), infection (MESH:D007239), insomnia (MESH:D007319), diverticulitis (MESH:D004238), COVID-19 (MESH:D000086382), death (MESH:D003643), ataxia (MESH:D001259), pain (MESH:D010146), Sleep dysfunction (MESH:D012893), intracerebral hemorrhages (MESH:D002543), PD (MESH:D010300), choreic dyskinesia (MESH:D002819), bradykinesia (MESH:D018476), CDS (MESH:D014202), abscess (MESH:D000038), inflammation (MESH:D007249), Globus Pallidus (MESH:D000079564), dysphagia (MESH:D003680), dyskinetic (MESH:D002547), pruritus (MESH:D011537), cognitive decline (MESH:D003072), aDBS (MESH:D018489), motor impairment (MESH:D000068079), seizure (MESH:D012640), Intestinal Infusions (MESH:D007410), PTT (MESH:D014570), IGP (MESH:C564543), rigidity (MESH:D009127), erythema (MESH:D004890), intestinal obstruction (MESH:D007415), paresthesias (MESH:D010292), sleep-related symptoms (MESH:D020183), dysarthria (MESH:D004401), akinesia (MESH:C537921), diarrhea (MESH:D003967), gait dysfunction (MESH:D020233), speech disturbance (MESH:D013064), cellulitis (MESH:D002481), bruising (MESH:D003288), GI hemorrhage (MESH:D006470), gait disequilibrium (MESH:D020234), Dyskinesia (MESH:D004409)
- **Chemicals:** azathioprine (MESH:D001379), basiliximab (MESH:D000077552), Apomorphine (MESH:D001058), Levodopa carbidopa (MESH:C009265), carbidopa (MESH:D002230), tacrolimus (MESH:D016559), cyclosporine (MESH:D016572), CSAI (-), prednisolone (MESH:D011239), L-DOPA (MESH:D007980), DA (MESH:D004298), CD (MESH:D002104), entacapone (MESH:C071192), prednisone (MESH:D011241), methylprednisolone (MESH:D008775)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12916957/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916957/full.md

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Source: https://tomesphere.com/paper/PMC12916957