Bapineuzumab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized (from mouse) |
| Target | beta-amyloid (Aβ) |
| Clinical data | |
| ATC code |
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| Identifiers | |
| CAS Number | |
| ChemSpider |
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| UNII | |
| ECHA InfoCard | 100.133.214 |
| Chemical and physical data | |
| Formula | C6466H10018N1734O2026S44 |
| Molar mass | 145874.02 g·mol−1 |
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Bapineuzumab (nicknamed "bapi")[1] is a humanized monoclonal antibody that acts on the nervous system and may have potential therapeutic value for the treatment of Alzheimer's disease and possibly glaucoma.[2] However, in 2012 it failed to produce significant cognitive improvements in patients in two major trials, despite lowering key biomarkers of AD, amyloid brain plaque and hyperphosphorylated tau protein in CSF.[3][4]
Bapineuzumab has been shown to recognise the extreme N-terminal 5 residues of Aβ peptide in a helical conformation (4HIX.pdb) stabilized by internal hydrogen bonds involving the first three amino acids.[5]
Bapineuzumab is an antibody to the beta-amyloid (Aβ) plaques that are believed to underlie Alzheimer's disease neuropathology. In previous clinical trials for vaccination against human beta amyloid, called AN-1792, patients with Alzheimer's disease using active immunization had positive outcomes with removal of plaques, but 6% of subjects developed aseptic meningitis and the trial was stopped.[6]
Testing
[edit]Bapineuzumab was being co-developed by the pharmaceutical companies Élan and Wyeth and entered Phase III trials in December 2007.[7] In 2008 a Johnson & Johnson affiliate acquired a substantial portion of Élan's assets related to the Alzheimer's immunotherapy program, which Elan had shared with Wyeth. The program is continuing with Pfizer, which acquired Wyeth in 2009.
Bapineuzumab was the first antibody to be found to cause amyloid-related imaging abnormalities, including an accumulation of fluid in brain tissue (ARIA-E)[8] in patients receiving the highest dose. No health risks were found in subjects receiving either 0.5 or 1 mg of bapineuzumab. Patients who have been receiving or have been scheduled to receive the highest dose will be either removed from the trials or switched to lower doses.[9]
The efficacy of drugs targeted to brain plaques in Alzheimer's patients has been called into question, although such drugs may still be effective for prophylaxis if given to individuals who have not yet developed clinical symptoms.[10][11]
On August 6, 2012, Pfizer Inc. and Johnson & Johnson said they are ending development of an intravenous formulation of bapineuzumab. Testing showed the drug did not work better than placebo in two late-stage trials in patients who had mild to moderate Alzheimer's disease.[11]
Élan announced that Johnson & Johnson, on July 16, 2013, had discontinued Phase 2 testing of the subcutaneous formulation of bapineuzumab.[12]
Insider trading
[edit]Mathew Martoma, formerly of S.A.C. Capital Advisors, was convicted in February 2014 of insider trading[13] on news passed by neurologist Sid Gilman of the cancellation of bapineuzumab's testing.[14]
References
[edit]- ^ Brandt C (Fall–Winter 2012). ""Team Babcock's" journey" (PDF). InSight. The Penn Memory Center (Penn Medicine): 1–3. Archived from the original (PDF) on 28 February 2014. Retrieved 1 Feb 2014.
- ^ Sample I (2007-08-07). "New Alzheimer's drugs might help prevent glaucoma". The Guardian. Retrieved 2008-06-18.
- ^ Berkrot B (7 August 2012). "Pfizer, J&J scrap Alzheimer's research as drug fails". Reuters.
- ^ "Alzheimer's disease drug shelved after trial failure". BBC News. 7 August 2012.
- ^ Miles LA, Crespi GA, Doughty L, Parker MW (2013-02-18). "Bapineuzumab captures the N-terminus of the Alzheimer's disease amyloid-beta peptide in a helical conformation". Scientific Reports. 3 (3): 1302. Bibcode:2013NatSR...3E1302M. doi:10.1038/srep01302. PMC 3575012. PMID 23416764.
- ^ Woodhouse A, Dickson TC, Vickers JC (2007). "Vaccination strategies for Alzheimer's disease: A new hope?". Drugs & Aging. 24 (2). Adis International: 107–19. doi:10.2165/00002512-200724020-00003. PMID 17313199. S2CID 28279428. Archived from the original on 2013-01-16. Retrieved 2010-07-27.
The vigour of international research on immunotherapy for AD provides significant hope for a strong therapeutic lead for the escalating number of individuals who will develop this otherwise incurable condition.
- ^ "Elan and Wyeth Announce Encouraging Top-line Results from Phase 2 Clinical Trial of Bapineuzumab for Alzheimer's Disease" (Press release). Elan Corporation. 2008-06-17. Archived from the original on 2013-01-22. Retrieved 2008-06-18.
Elan and Wyeth plan to continue all four studies in the previously disclosed bapineuzumab Phase 3 clinical program
- ^ DiFrancesco JC, Longoni M, Piazza F (2015-09-25). "Anti-Aβ Autoantibodies in Amyloid Related Imaging Abnormalities (ARIA): Candidate Biomarker for Immunotherapy in Alzheimer's Disease and Cerebral Amyloid Angiopathy". Frontiers in Neurology. 6: 207. doi:10.3389/fneur.2015.00207. PMC 4585101. PMID 26441825.
- ^ Pogatchnik S (2009-04-02). "Drug Makers Stop Top Dosage in Alzheimer's Trial". Drug Discovery & Development. Retrieved 2009-04-16.
- ^ Steenhuysen J (May 12, 2010). "New theory of Alzheimer's explains drug failures". Reuters. Chicago: Reuters. p. 2.
- ^ a b Berkrot B (August 7, 2012). "Pfizer, J&J scrap Alzheimer's studies as drug fails". Reuters. New York. Retrieved August 7, 2012.
- ^ Phase 2 testing of the subcutaneous formulation of bapineuzumab is to be discontinued. Elan Corporation. Retrieved 2013-08-13.
- ^ Stevenson A, Goldstein M (February 7, 2014). "Ex-SAC Trader Convicted of Securities Fraud". The New York Times. p. A1. Retrieved February 22, 2014.
- ^ Betzold M (2013-01-26). "The Corruption of Sid Gilman-How a top U-M doc lost his way". Ann Arbor Observer. Archived from the original on 2014-02-28. Retrieved 24 February 2014.