Study of Octagam (Intravenous Immunoglobulin [IVIG]) 10% on the Treatment of Mild to Moderate Alzheimer's Disease

Octapharma

Status and phase: Completed; Phase 2

Conditions: Alzheimer's Disease

Treatments: Biological: octagam 10%; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT00812565

GAM10-04

Details and patient eligibility

About

This study evaluated the effect of 6 or 12 infusions of different doses of octagam (intravenous immunoglobulin [IVIG]) 10% on the reduction of amyloid beta peptide (Aβ) in cerebral spinal fluid (CSF) and on the increase of Aβ in blood plasma in patients with mild to moderate Alzheimer's disease.

Full description

Participants received 12 infusions of 0.1 g/kg, 0.25 g/kg, or 0.4 g/kg body weight octagam 10% at 2-week intervals (±3 days) or 6 infusions of 0.2 g/kg, 0.5 g/kg, or 0.8 g/kg body weight octagam 10% at 4-week intervals (±5 days). The effect of the infusions on the reduction of Aβ peptide in CSF and the increase of Aβ peptide in blood plasma was evaluated.

Enrollment: 58 patients

Sex: All

Ages: 50 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Probable Alzheimer's Disease (AD) according to the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria.
• Age of 50 to 85.
• Mini-mental State Examination (MMSE) score of 16 to 26.
• Sufficient language skills for testing.
• Sufficient vision and hearing for testing.
• Modified Hachinski-Rosen Score < 5.
• Magnetic resonance imaging (MRI) of the head consistent with the diagnosis of AD.
• Caregiver available with contact at least 4 days per week for greater than 1 hour.
• Outpatient status or assisted living.
• Post-menopause (women) as evidenced by lack of menstruation for at least 12 consecutive months or by having bilateral oophorectomy.
• Stable doses of approved AD medication(s) for at least 3 months prior to screening (eg, acetylcholine esterase (AChE) inhibitors, memantine).
• Normal vital signs or clinically insignificant, if outside normal limits.
• Laboratory findings within normal limits or clinically insignificant, if outside normal limits.
• Normal electrocardiogram (ECG) or clinically not significant, if outside normal limits.

Exclusion criteria

• Other causes of dementia (eg, vascular dementia, Lewy-body dementia, fronto-temporal dementia, Creutzfeldt-Jacob disease, Huntington's disease, Parkinson's disease).
• History of or present significant other diseases of the central nervous system (eg, brain tumor, normal pressure hydrocephalus, Parkinson's Disease, stroke, severe brain trauma, brain surgery, epilepsy, encephalitis).
• Geriatric depression scale score > 7 (short form with scale from 0 to 15).
• Present significant psychiatric disorder (eg, major depression).
• History of psychosis or hallucinations.
• Mental retardation.
• Unstable medical disease in the opinion of the investigator.
• Insulin dependent diabetes mellitus.
• Acute infectious disease.
• Vitamin B12 deficiency unless on stable replacement therapy for at least 3 months is acceptable.
• Unstable thyroid dysfunction.
• Uncontrolled hypertension.
• Severe liver or kidney disease.
• Major surgery within 3 months prior to screening.
• Prohibited medications: Antiepileptic drugs, antipsychotics (but allowed for treatment of acute episodes), antiparkinson agents, anticholinergic drugs, selegiline, monoamine oxidase inhibitors (MAOI), tricyclics, immunosuppressive medications, anti-histamines (unless on a stable dose for at least 3 months or used for treatment of acute episodes), benzodiazepines (but allowed for treatment of acute episodes), and lithium.
• Antidepressants are permitted, if on a stable dose for at least 3 months and without significant anticholinergic side-effects.
• Peripheral venous conditions which impair establishing regular venous access for infusions.
• Potential reasons that patient may become non-evaluable during the study (eg, planned moving into a nursing home, but assisted living is acceptable).
• Peripheral venous conditions, which impair establishing regular venous access for infusions.
• Known IgA deficiency with antibodies to IgA.
• History of hypersensitivity to blood or plasma derived products, or any component of octagam 10%, such as maltose.
• Medical conditions which interfere with protein catabolism (eg, nephrotic syndrome).
• Known blood hyperviscosity or other hypercoagulable states.
• Deep vein thrombosis within preceding 4 years.
• Symptomatic stroke.
• Transient ischemic attack (TIA) within preceding 2 years.
• Participation in another drug trial within the previous 3 months before screening.
• Participation in immunological treatment studies of AD other than with intravenous immunoglobulin (IGIV) within the previous 6 months before screening.
• IGIV use in the previous 6 months.
• Live viral vaccination within the last month before study entry.
• Not eligible for lumbar puncture (anticoagulant therapy, coagulation disorders, severe spinal alterations).
• Patients with a past or present history of drug abuse or alcohol abuse within the preceding 5 years.
• Patients with any condition that would make the patient, in the opinion of the Investigator, unsuitable for the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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58 participants in 8 patient groups, including a placebo group

Placebo every 2 weeks

Placebo Comparator group

Description:

Participants received placebo intravenously every 2 weeks for 24 weeks (total of 12 infusions).

Treatment:

Drug: Placebo

0.1 g/kg octagam 10% every 2 weeks

Experimental group

Description:

Participants received 0.1 g/kg octagam 10% intravenously every 2 weeks for 24 weeks (total of 12 infusions).

Treatment:

Biological: octagam 10%

0.25 g/kg octagam 10% every 2 weeks

Experimental group

Description:

Participants received 0.25 g/kg octagam 10% every 2 weeks for 24 weeks (total of 12 infusions).

Treatment:

Biological: octagam 10%

0.4 g/kg octagam 10% every 2 weeks

Experimental group

Description:

Participants received of 0.4 g/kg octagam 10% every 2 weeks for 24 weeks (total of 12 infusions).

Treatment:

Biological: octagam 10%

Placebo every 4 weeks

Placebo Comparator group

Description:

Participants received placebo intravenously every 4 weeks for 20 weeks (total of 6 infusions).

Treatment:

Drug: Placebo

0.2 g/kg octagam 10% every 4 weeks

Experimental group

Description:

Participants received 0.2 g/kg octagam 10% intravenously every 4 weeks for 20 weeks (total of 6 infusions).

Treatment:

Biological: octagam 10%

0.5 g/kg octagam 10% every 4 weeks

Experimental group

Description:

Participants received 0.5 g/kg octagam 10% every 4 weeks for 20 weeks (total of 6 infusions).

Treatment:

Biological: octagam 10%

0.8 g/kg octagam 10% every 4 weeks

Experimental group

Description:

Participants received of 0.8 g/kg octagam 10% every 4 weeks for 20 weeks (total of 6 infusions).

Treatment:

Biological: octagam 10%