Clinical trial protocol: TRANSCEND 1 – an observational study of patients with moderate Parkinson’s disease
Paul-Visse Gesine1, Håkan Widner2, Regine Bergholdt3, Helle Frimer-Larsen4, Ida Stenfeldt Mathiasen3, Anne Møller Nielsen4, Roger Barker5
1Translational Neurology Group, Lund University, 2Skåne University Hospital, 3Stem cell R&D, Novo Nordisk A/S, 4Development, Novo Nordisk A/S, 5WT-MRC Cambridge Stem Cell Institute/Department of Clinical Neuroscience, University of Cambridge
Objective:

An observational study ahead of the proof-of-concept transplant trial may reduce some of the confounding factors associated with investigating therapies in Parkinson’s disease. TRANSCEND 1 will follow a cohort of patients with Parkinson’s disease receiving a local standard of care (SoC) to monitor fluctuations in individual performance and disease characteristics over time and to facilitate a reliable baseline of disease severity before a subsequent proof-of-concept trial with a novel stem-cell based treatment in some patients from this cohort.

Background:

Novo Nordisk is developing a cell therapy for Parkinson’s disease in collaboration with groups at Lund University (Sweden) and the University of Cambridge (UK). The therapy comprises dopaminergic progenitor cells derived from human embryonic stem cells; the clinical development programme currently includes this observational study (TRANSCEND 1) and a planned phase 1/2, proof-of-concept transplant trial (TRANSCEND 2).

Design/Methods:

Patients (n=96) with moderate Parkinson’s disease (50–68 years old), with fluctuating disease and a disease duration of >5 years, will be followed for up to 24 months. Patients will be examined every 3 months using standard motor (MDS-UPDRS III), cognitive (MoCA), psychiatric (MADRS) and other clinical measures. Patients will receive SoC which may lead to changes in their medication regimen. However, the participants are required to have ≥2 rounds of assessments and 3 months of observation without medication adjustments prior to being invited to be screened for participation in the proof-of-concept transplant trial.

Results:

The study will start recruiting in February 2023.

Conclusions:
Results are expected in 2025.
10.1212/WNL.0000000000203522