Tolerability and Safety of Subcutaneous Administration of AFFITOPE AD02 in Mild to Moderate Alzheimer's Disease

NCT ID: NCT00633841

Last Updated: 2010-10-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-02-29
• Study Completion Date: 2009-09-30

Brief Summary

The purpose of this study is to assess the tolerability and safety of repeated subcutaneous injection of a single dose of AFFITOPE AD02 in patients with mild to moderate Alzheimer's Disease.

Detailed Description

Alzheimer's Disease (AD) is a devastating neurodegenerative disorder for which there is no cure.

Although the etiology of AD is not fully understood, recent research suggests that Aβ is central to the disease process. Consequently, approaches capable of removing Aβ from the brain, such as Aβ immunotherapy, are expected to possess disease-modifying potential. This view is supported by evidence gathered in mouse models of AD and studies involving AD patients.

Based on the view that active Aβ immunotherapy has disease-modifying potential both in animal models of AD and in patients, and on the knowledge gathered on the side-effects of Aβ-based immunotherapy encountered in humans, we designed a new generation of AD vaccines. Rather than using full length Aβ itself, we choose to use mimotopes of the N-terminal end of Aβ as the antigenic component of our vaccine (Mimotopes discovered by Affiris GmbH have been termed AFFITOPES). Mimotopes are peptides that functionally mimic the native antigenic epitope but do not show sequence identity to it. Thus, while being different from the original antigen, mimotopes are recognized by the same antibodies and, vice versa, are capable of inducing antibodies that cross-react with the original antigen itself. A major advantage offered by mimotopes is the lack of tolerance mechanisms that would prevent the induction of an immune response to it (as is the case with self peptides/proteins such as Aβ). To further increase the vaccine's safety profile, the length of the mimotope used was limited to preclude the elicitation of Aβ-specific T cells. Also, the mimotope used has been designed to generate antibodies directed exclusively to Aβ (i.e., they do not recognize parental APP itself). To provide helper epitopes for the generation of an antibody response, the mimotope is coupled to a carrier.

The trial is designed as a patient-blinded, single-center, randomized, controlled, parallel group, phase I clinical study of repeated once every 4 weeks administration by subcutaneous injection of AFFITOPE AD02 alone or adsorbed to aluminium hydroxide in 24 patients with mild to moderate Alzheimer's Disease. In total, each patient will receive 4 immunizations. Patients will be randomized to receive AFFITOPE AD02 alone or adsorbed to alumimium hydroxide. Each treatment group consists of 12 patients. For safety reasons, inclusion of patients will be done in a stepwise manner.

Conditions

Alzheimer's Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

1

AFFITOPE AD02 without adjuvant

Group Type: ACTIVE_COMPARATOR

AFFITOPE AD02

Intervention Type: BIOLOGICAL

4 subcutaneous injections of IP in 4-week intervals

2

AFFITOPE AD02 with adjuvant

Group Type: ACTIVE_COMPARATOR

AFFITOPE AD02

Intervention Type: BIOLOGICAL

4 subcutaneous injections of IP in 4-week intervals

Interventions

AFFITOPE AD02

4 subcutaneous injections of IP in 4-week intervals

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Diagnosis of probable Alzheimer's disease based on the NINCDS/ADRDA criteria.
• Alzheimer's disease of mild to moderate degree (MMSE 16-26)
• Magnetic Resonance Imaging scan (MRI) of brain consistent with diagnosis of AD.
• Written informed consent signed and dated by the patient and the caregiver.
• Age 50-80 years.
• Availability of a partner/caregiver

Exclusion Criteria

• Presence or history of allergy to components of the vaccine.
• Contraindication for MRI imaging.
• Participation in another clinical trial.
• Prior and/or current treatment with experimental immunotherapeutics including IVIG or vaccines for AD.
• Prior and/or current treatment with immunosuppressive drugs
• History and/or presence of autoimmune disease.

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Affiris AG

INDUSTRY

Sponsor Role: lead

Principal Investigators

Margot Schmitz, Univ. Doz. Dr.

Role: PRINCIPAL_INVESTIGATOR

Ordination Univ. Doz. Dr. Margot Schmitz

Locations

Ordination Univ. Doz. Dr. Margot Schmitz

Vienna, , Austria

Countries

Austria

Other Identifiers

Affiris 002

Identifier Type: -

Identifier Source: org_study_id