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Encapsulated Cell Biodelivery of Nerve Growth Factor to Alzheimer´s Disease Patients

An Open Label, Dose-Escalation Study of Encapsulated Cell Biodelivery of Nerve Growth Factor to the Cholinergic Basal Forebrain of Alzheimer´s Disease Patients

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01163825
Acronym
NsG0202
Enrollment
6
Registered
2010-07-16
Start date
2008-01-31
Completion date
Unknown
Last updated
2010-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease

Brief summary

Cholinergic neurons in the basal forebrain project widely to the cerebral cortex and hippocampus. These neurons depend on nerve growth factor (NGF) from their target areas for survival. Impaired NGF supply is part of the Alzheimer's disease (AD) pathology, and the degeneration of these neurons correlates with the cognitive decline in these patients. The objective of encapsulated cell biodelivery (ECB) is to maintain normal levels of NGF to support cholinergic function. NsGene's NGF secreting ECB device (NsG0202) combines the potential benefits of targeted gene therapy with the safety of a retrievable implantable device. The study is an open label, single centre, 12-month, dose-escalation phase Ib study in patients with mild to moderate AD. The primary objective is safety and tolerability, while secondary outcomes measure include cognition, behaviour, neuropsychology, activities of daily living (ADL), positron emission tomography (PET) imaging and electroencephalography (EEG).

Interventions

Encapsulated cell biodelivery of Nerve Growth Factor (NGF) to the basal forebrain nuclei of the brain by multiple implantable devices housing NGF-secreting human cells

Sponsors

Karolinska Institutet
CollaboratorOTHER
Region Stockholm
CollaboratorOTHER_GOV
NsGene A/S
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age 50-80 years 2. All patients must fulfil the NINDNDS-ARDRA criteria of Alzheimer's disease. 3. The subject must have a score between 15-24 inclusive, on the mini-mental state examination (MMSE). 4. The subject must have a caregiver who is able and committed to assist the subject to comply with the trial protocol, and who is willing to provide the information required at assessment interviews. 5. Informed consent must be obtained from the subject together with a close caregiver, in accordance with the requirements of the ethical committee.

Exclusion criteria

1. A diagnosis of Schizophrenia, Schizo-affective disorder or paranoid disorder according to DSM IV without any suspicion cognitive decline. 2. Patients with the following co-existing medical conditions: 3. History of seizures. 4. Brain tumor including meningeoma. 5. Clinically significant hepatic, renal, pulmonary, metabolic or endocrine disturbances. 6. Clinically significant back pain. 7. Bleeding disorders. 8. Patients who, in the opinion of the investigator, are otherwise unsuitable for a trial of this type.

Design outcomes

Primary

MeasureTime frame
Adverse events12 months

Secondary

MeasureTime frameDescription
Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-Cog)12 monthsCognition using ADAS-Cog, neuropsychologic test battery

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026