CERE-110 in Subjects With Mild to Moderate Alzheimer's Disease
A Phase I, Dose-Escalating Study to Assess the Safety and Tolerability of CERE-110 [Adeno-Associated Virus (AAV)-Based Vector-Mediated Delivery of Beta-Nerve Growth Factor (NGF)] in Subjects With Mild to Moderate Alzheimer's Disease
  • Phase

    Phase 1
  • Study Type

  • Status

    Completed No Results Posted
  • Intervention/Treatment

    cere-110 ...
  • Study Participants

This is a Phase I clinical study to assess the safety, tolerability and biologic activity of in vivo AAV-mediated delivery of CERE-110. Up to 12 subjects will receive open label CERE-110 in dose-escalating fashion. All subjects will receive bilateral, stereotactic injections of CERE-110 for a total of four (Dose A and B) and six (Dose C) injections to target the basal forebrain region of the brain containing the nucleus basalis of Meynert (NBM). All study participants will be observed for a 24-month period and then followed annually.
Study Started
Jun 30
Primary Completion
May 31
Study Completion
May 31
Last Update
Nov 10

Genetic CERE-110: Adeno-Associated Virus Delivery of NGF

CERE-110 2.0 x 10^10 vg, CERE-110 1.0 x 10^11 vg, CERE-110 2.0 x 10^11 vg


Inclusion Criteria:

Alzheimer's disease as determined by NINCDS/ADRDA criteria.
Score of ≤ 4 on a modified Hachinski Ischemia Scale
Mini-Mental State Exam (MMSE) score in the range of 16 to 28, inclusive
No significant neurological or medical abnormalities contraindicating surgery, MRI/PET imaging or study participation
Subjects stable on standard-of-care medications (i.e., acetylcholinesterase inhibitors) for Alzheimer's disease for 3 months prior to entry
A Hamilton Depression Scale score of ≤ 12 on a 17-item scale and no history of major depressive episode within the last 2 years
A score of < 15 on the Beck Depression Inventory
Adequate visual and auditory acuity to allow neuropsychological testing
Good health with no clinically significant medical or psychological conditions
An MRI of the head at screen that is negative for evidence of infection, tumor, infarction or other focal (e.g., subdural hematoma) or generalized lesions(e.g., v hydrocephalus) and without clinical symptoms suggestive of intervening neurological disease
Normal serum B12, thyroid function tests, and negative syphilis antibody test
The informed consent document must be signed by both:

a competent and willing subject, and a surrogate identified by the participant, or a legally authorized power of attorney for Health Care, or a family member

Exclusion Criteria:

History of cancer within the last five years, except superficial basal or squamous cell skin cancer or cervical carcinoma in situ
History of alcohol abuse or dependence within the last two years
Liver serum transaminases (AST and/or ALT) > 5 times the upper limit of normal; total and/or direct bilirubin > 1.5 mg/dL, hemoglobin < 9mg/dL; PT and PTT > 2 times the upper limit of normal; creatinine clearance < 30 mL/min; positive serology for HBV or HCV; absolute neutrophil count < 1,500 cells/mm3 and a platelet count < 100,000/mm3
Any significant systemic illness, unstable or severe medical condition(s) that could put the subject at risk during the study, interfere with outcome measures or affect compliance with the protocol procedures
Centrally active beta-blockers, anti-Parkinsonian medications, psychostimulants, antipsychotics, neuroleptics, or narcotic analgesics, long-acting benzodiazepines or barbiturates, hypertensive agents with a CNS effect, short-acting anxiolytics or sedative hypnotics more frequently than two times per week within 14 days of screening, herbal products for Alzheimer's disease, antidepressants with significant cholinergic side effects (e.g., tricyclics), initiation or change in dose of standard treatment for Alzheimer's disease
Other medication with significant cholinergic or anticholinergic side effects
Warfarin (coumadin), nonsteroidal anti-inflammatory drugs, aspirin, Prozac, or Ginkgo biloba within 14 days of surgery
Subjects who have received investigational agents or been exposed to investigational devices for 30 days prior to enrollment
Subjects with a history of receiving gene transfer products of any kind
Subjects who cannot undergo MRI or PET screening
No Results Posted