Literature DB >> 32666599

Human Fetal Cell Therapy in Huntington's Disease: A Randomized, Multicenter, Phase II Trial.

Anne-Catherine Bachoud-Lévi1,2,3.   

Abstract

BACKGROUND: Huntington's disease is a rare, severe, inherited neurodegenerative disease in which we assessed the safety and efficacy of grafting human fetal ganglionic eminence intrastriatally.
METHODS: Patients at the early stage of the disease were enrolled in the Multicentric Intracerebral Grafting in Huntington's Disease trial, a delayed-start phase II randomized study. After a run-in period of 12 months, patients were randomized at month 12 to either the treatment group (transplanted at month 13-month 14) or the control group and secondarily treated 20 months later (month 33-month 34). The primary outcome was total motor score compared between both groups 20 months postrandomization (month 32). Secondary outcomes included clinical, imaging, and electrophysiological findings and a comparison of pregraft and postgraft total motor score slopes during the entire study period (month 0-month 52) regardless of the time of transplant.
RESULTS: Of 54 randomized patients, 45 were transplanted; 26 immediately (treatment) and 19 delayed (control). Mean total motor score at month 32 did not differ between groups (treated controls difference in means adjusted for M12: +2.9 [95% confidence interval, -2.8 to 8.6]; P = 0.31). Its rate of decline after transplantation was similar to that before transplantation. A total of 27 severe adverse events were recorded in the randomized patients, 10 of which were related to the transplant procedure. Improvement of procedures during the trial significantly decreased the frequency of surgical events.We found antihuman leucocytes antigen antibodies in 40% of the patients.
CONCLUSION: No clinical benefit was found in this trial. This may have been related to graft rejection. Ectopia and high track number negatively influence the graft outcome. Procedural adjustments substantially improved surgical safety. (ClinicalTrials.gov NCT00190450.)
© 2020 International Parkinson and Movement Disorder Society. © 2020 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  Huntington's disease; MIG-HD; cell therapy; phase 2 trial

Mesh:

Year:  2020        PMID: 32666599     DOI: 10.1002/mds.28201

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   9.698


  5 in total

1.  Cell Therapy for Huntington's Disease: Learning from Failure.

Authors:  Anne E Rosser; Monica Busse; Romina Aron Badin; Josep M Canals; Vicki Wheelock; Anselme L Perrier; William Gray; Leslie Thompson; Steven Goldman
Journal:  Mov Disord       Date:  2021-03       Impact factor: 9.698

2.  Protocol for an open label: phase I trial within a cohort of foetal cell transplants in people with Huntington's disease.

Authors:  Cheney J G Drew; Feras Sharouf; Elizabeth Randell; Lucy Brookes-Howell; Kim Smallman; Bernadette Sewell; Astrid Burrell; Nigel Kirby; Laura Mills; Sophie Precious; Philip Pallmann; David Gillespie; Kerry Hood; Monica Busse; William P Gray; Anne Rosser
Journal:  Brain Commun       Date:  2021-01-19

Review 3.  Molecular Components of Store-Operated Calcium Channels in the Regulation of Neural Stem Cell Physiology, Neurogenesis, and the Pathology of Huntington's Disease.

Authors:  Ewelina Latoszek; Magdalena Czeredys
Journal:  Front Cell Dev Biol       Date:  2021-04-01

4.  Translating cell therapies for neurodegenerative diseases: Huntington's disease as a model disorder.

Authors:  Anne E Rosser; Monica E Busse; William P Gray; Romina Aron Badin; Anselme L Perrier; Vicki Wheelock; Emanuele Cozzi; Unai Perpiña Martin; Cristina Salado-Manzano; Laura J Mills; Cheney Drew; Steven A Goldman; Josep M Canals; Leslie M Thompson
Journal:  Brain       Date:  2022-06-03       Impact factor: 15.255

Review 5.  Do foetal transplant studies continue to be justified in Huntington's disease?

Authors:  Oliver J M Bartley; Mariah J Lelos; William P Gray; Anne E Rosser
Journal:  Neuronal Signal       Date:  2021-12-13
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.