Orchard Therapeutics (Europe) Limited

Address
245 Hammersmith Road

Sponsor Overview

assignment
6
sponsored trials
science
8
molecules
location_city
7
research centres
public
5
countries
person_search
10
investigators

Specializations

Metachromatic Leukodystrophy and related lysosomal storage disorders

Orchard Therapeutics (Europe) Limited supports clinical research in Metachromatic Leukodystrophy, including late juvenile MLD and broader ARSA deficiency manifestations. The funded studies focus on neurological outcomes, disease progression, and restoration of enzyme activity in affected tissues.

  • MLD
  • Late juvenile MLD
  • Motor impairment
  • Residual ARSA activity

Research activity in this area is centered on gene therapy approaches designed for inherited neurodegenerative disease.

Mucopolysaccharidosis type I and Hurler syndrome

The sponsor funds studies in Mucopolysaccharidosis type I, including the severe childhood form known as Hurler syndrome. These trials examine treatment options aimed at addressing the underlying metabolic defect and supporting clinical benefit in pediatric patients.

  • MPS-IH
  • Hurler syndrome
  • IDUA gene
  • Pediatric lysosomal disease

Clinical interest in this domain includes autologous hematopoietic stem cell approaches for inherited metabolic disorders.

Hematopoietic stem cell gene therapy

Orchard Therapeutics focuses on hematopoietic stem cell-based gene therapy programs that use genetically modified autologous cells to treat inherited diseases. The clinical portfolio includes investigations of cell-enriched products and lentiviral vector-enabled gene delivery.

  • Autologous CD34+ cells
  • HSPC transduction
  • Lentiviral vector
  • Cell-based gene transfer

These studies reflect a strong therapeutic interest in correcting inherited enzyme deficiencies through ex vivo cellular engineering.

Neurological and motor function outcomes

The sponsor’s trials place emphasis on neurological disease burden, including central nervous system involvement, peripheral nervous system involvement, and changes in functional performance. Outcomes include clinical measures of motor impairment and disease-related disability in children and young people.

  • Clinical motor impairment
  • GMFM scoring
  • Neurological progression
  • Functional disability

This area links the sponsor’s work to disorders where preserving movement, coordination, and neurological function is central to treatment evaluation.

Sponsored Trials

Data & Insights

science
Molecule Portfolio
Compounds under investigation
3
Exclusive Molecules
out of 8 total (38% not shared with other sponsors)

This sponsor works with 8 molecules, of which 3 are not being studied by other sponsors.

hub
Site Partnerships
Collaboration with research centres
14%
Return partnership rate
1 of 7 sites collaborated multiple times

This sponsor has worked with 7 sites across their trial portfolio.

Therapeutic Focus

  • 1.
    Genetic Phenomena4 trials
    26 other sponsors
  • 2.
    Congenital, Hereditary, and Neonatal Diseases and Abnormalities1 trial
    165 other sponsors
  • 3.
    Musculoskeletal Diseases1 trial
    238 other sponsors
  • 4.
    Nutritional and Metabolic Diseases1 trial
    211 other sponsors

Partnered Research Centres

7 centres
location_city
assignment155
Amsterdam UMC
Address
Meibergdreef 9, 1105 AZ Amsterdam
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location_city
assignment65
Bicetre Hospital
Address
78 Rue Du General Leclerc, 94275 Le Kremlin-Bicetre
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location_city
assignment848
Ospedale San Raffaele S.r.l.
Address
Via Olgettina 60, 20132 Milan
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location_city
assignment94
Prinses Maxima Centrum voor Kinderoncologie B.V.
Address
Heidelberglaan 25, 3584 CS Utrecht
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location_city
assignment348
Region Skane Skanes Universitetssjukhus
Address
St. Johns, Fritz Bauers Gata 5, Malmo St. Johns, 214 28 Lund
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location_city
assignment628
Universitaetsklinikum Tuebingen AöR
Address
Otfried-Mueller-Strasse 10, Nordstadt, 72076 Tübingen
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