Tolerability and Safety of Subcutaneous Administration of Affitope AD01 in Mild to Moderate Alzheimer's Disease

• ClinicalTrials.gov Identifier: NCT00495417
• Recruitment Status: Completed
• First Posted: July 3, 2007
• Last Update Posted: October 19, 2010
• Sponsor: Affiris AG
• Information provided by: Affiris AG

Tracking Information

• First Submitted Date: July 2, 2007
• First Posted Date: July 3, 2007
• Last Update Posted Date: October 19, 2010
• Study Start Date: July 2007
• Actual Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
• Current Primary Outcome Measures (submitted: July 2, 2007): Tolerability [ Time Frame: One year ]
• Original Primary Outcome Measures: Same as current
• Current Secondary Outcome Measures (submitted: July 2, 2007): Immunological and clinical efficacy (evaluated in explorative manner) [ Time Frame: One year ]
• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Tolerability and Safety of Subcutaneous Administration of Affitope AD01 in Mild to Moderate Alzheimer's Disease
• Official Title: Randomized, Controlled, Parallel Group, Patient-blinded, Single-center Phase I Pilot Study to Assess Tolerability and Safety of Repeated s.c. Administration of a Single-dose of Affitope AD01 Applied With or Without Adjuvant to Patients With Mild to Moderate Alzheimer's Disease
• Brief Summary: The purpose of this study is to assess the tolerability and safety of repeated subcutaneous injection of a single dose of Affitope AD01 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 AD01 alone or adsorbed to aluminum 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 AD01 alone or adsorbed to aluminum hydroxide. Each treatment group consists of 12 patients. For safety reasons, inclusion of patients will be done in a stepwise manner.

• Study Type: Interventional
• Study Phase: Phase 1
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: Single (Participant); Primary Purpose: Treatment
• Condition: Alzheimer's Disease

Intervention

• Biological: AFFITOPE AD01
  s.c. injection
• Biological: AFFITOPE AD01 adjuvanted
  s.c. injection

Study Arms

• Active Comparator: 1
  Intervention: Biological: AFFITOPE AD01
• Active Comparator: 2
  Intervention: Biological: AFFITOPE AD01 adjuvanted

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: July 2, 2007): 24
• Original Estimated Enrollment: Same as current
• Actual Study Completion Date: August 2009
• Actual Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Diagnosis of probable Alzheimer's disease based on the NINCDS/ADRDA criteria.
• Assessing the severity of Alzheimer's disease of mild to moderate degree by the Mini Mental State Examination (MMSE 16-26)
• Hachinski Ischemia Scale ≤ 4.
• Magnetic Resonance Imaging scan (MRI) of brain consistent with diagnosis of AD.
• Informed consent capability (as determined by an independent neurologist)
• Written informed consent signed and dated by the patient or the patient's legal representative and the caregiver.
• Age >50 years.
• Availability of a partner/caregiver knowing the patient and being able to accompany the patient to the visits and being available for the telephone interviews.
• Adequate visual and auditory acuity to allow neuropsychological testing.
• Female patients of childbearing potential using a medically accepted contraceptive method.
• AD therapies on stable doses for at least 3 months prior to Visit 1 and during the entire trial period.
• Stable doses of all other medications for at least 30 days prior to Visit 1 if considered relevant by the investigator.

Exclusion Criteria:

• Pregnant women.
• Sexually active women of childbearing potential not using a medically accepted birth control method.
• Presence or history of allergy to components of the vaccine.
• Contraindication for MRI imaging.
• Operation (under general anaesthesia) within 3 months prior to study entry and scheduled elective operation during the whole study period.
• Participation in another clinical trial.
• History of questionable compliance to visit schedule; patients not expected to complete the clinical trial.
• Prior and/or current treatment with experimental immunotherapeutics including IVIG or vaccines for AD.
• Prior and/or current treatment with immunosuppressive drugs, concurrent treatment with beta-blockers.
• History and/or presence of autoimmune disease.
• Recent (≤3 years since last specific treatment) history of cancer (Exceptions: basal cell carcinoma, intraepithelial cervical neoplasia).
• Major psychiatric disorder (e.g. schizophrenia), if considered relevant by the investigator.
• Active infectious disease (e.g., Hepatitis B, C).
• Presence and/or history of Immunodeficiency (e.g., HIV).
• Significant neurological disease other than AD.
• Significant systemic illness.
• History of stroke or seizure.
• Change in dose of standard treatments for AD within 3 months prior to visit 1.
• Change in dose of other previous and current medications within the last 30 days prior to visit 1, if considered relevant by the investigator.
• Alcoholism or substance abuse within the past year (alcohol or drug intoxication).

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 50 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Austria

Administrative Information

• NCT Number: NCT00495417
• Other Study ID Numbers: Affiris 001; EUDRACT Number 2006-007063-90
• Has Data Monitoring Committee: Yes
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Current Responsible Party: Affiris GmbH
• Original Responsible Party: Not Provided
• Current Study Sponsor: Affiris AG
• Original Study Sponsor: Same as current
• Collaborators: Not Provided

Investigators

• Principal Investigator: Markus Müller, UnivProf.Dr.; Medical University of Vienna

• PRS Account: Affiris AG
• Verification Date: September 2009