Open access · US-GOV via ClinicalTrials.gov Clinical trial

A Phase 2a, Multicenter, Randomized, Third-party Un-blinded, Long-term Extension Study To Determine Safety, Tolerability, And Immunogenicity Of Acc-001 With Qs-21 Adjuvant In Subjects With Mild To Moderate Alzheimer Disease

Authors not listed

Pfizer · 2009

Dysbiosis Human Randomized controlled trial

Abstract

The purpose of this study is to assess the long term safety, tolerability, and immunogenicity of ACC-001, an investigational vaccine, plus QS-21 in subjects with mild to moderate Alzheimer's disease.

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Source: ClinicalTrials.gov
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Fetched: 2026-11-02 MST

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APA

Anonymous. (2009). A Phase 2a, Multicenter, Randomized, Third-party Un-blinded, Long-term Extension Study To Determine Safety, Tolerability, And Immunogenicity Of Acc-001 With Qs-21 Adjuvant In Subjects With Mild To Moderate Alzheimer Disease. <em>Pfizer</em>. https://clinicaltrials.gov/study/NCT00960531

Vancouver

Anonymous. A Phase 2a, Multicenter, Randomized, Third-party Un-blinded, Long-term Extension Study To Determine Safety, Tolerability, And Immunogenicity Of Acc-001 With Qs-21 Adjuvant In Subjects With Mild To Moderate Alzheimer Disease. Pfizer. 2009.

BibTeX

@misc{anon2009APhase, title = {A Phase 2a, Multicenter, Randomized, Third-party Un-blinded, Long-term Extension Study To Determine Safety, Tolerability, And Immunogenicity Of Acc-001 With Qs-21 Adjuvant In Subjects With Mild To Moderate Alzheimer Disease}, author = {Anonymous}, journal = {Pfizer}, year = {2009}, }