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Monoclonal antibody
TypeWhole antibody
SourceHumanized
TargetIntegrin α4β7
Clinical data
Trade namesEntyvio
AHFS/Drugs.comMultum Consumer Information
ATC code
Legal status
Legal status
Identifiers
CAS Number
ChemSpider
UNII
Chemical and physical data
FormulaC6528H10072N1732O2042S42
Molar mass146.8 kDa g·mol−1
 ☒NcheckY (what is this?)  (verify)

Vedolizumab (trade name Entyvio) is a monoclonal antibody developed by Millennium Pharmaceuticals, Inc (a subsidiary of Takeda Pharmaceuticals) for the treatment of ulcerative colitis and Crohn's disease.[2] It binds to integrin α4β7 (LPAM-1, lymphocyte Peyer's patch adhesion molecule 1).[2][3] Blocking the α4β7 integrin results in gut-selective Anti-inflammatory activity.[4] It is marketed under the trade name Entyvio.[5]

Medical uses

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Ulcerative colitis

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Vedolizumab has been investigated in one main study in adult patients. Patients with moderate to severe active disease in whom conventional therapy or TNF-alpha antagonists were ineffective or could not be tolerated received either vedolizumab or Placebo. The main measure of effectiveness was the proportion of patients whose symptoms improved after 6 weeks of treatment. Vedolizumab was shown to be more effective than placebo: 47% (106 out of 225) of patients who received vedolizumab showed an improvement in symptoms, compared with 26% (38 out of 149) of patients who received placebo. The study also showed that vedolizumab maintained the effect up to 52 weeks more effectively than placebo.[6]

Crohn's disease

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In one main study in adult patients with moderate to severe active Crohn’s disease in whom conventional therapy or TNF-alpha antagonists were ineffective or could not be tolerated vedolizumab was shown to be more effective than placebo: 15% (32 out of 220) of patients receiving vedolizumab showed improved symptoms after 6 weeks of treatment, compared with 7% (10 out of 148) of patients on placebo. The maintenance of the effect up to 52 weeks was more effective with vedolizumab than with placebo.[6]

Specific Populations

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  • Pediatrics - safety has not been established in pediatric populations
  • Geriatrics - not enough data[7]

History

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The cell line used to develop vedolizumab was created by physician scientists at the Massachusetts General Hospital in Boston, Massachusetts, as a result of work executed at Dr. Robert B. Colvin's lab, from the Department of Pathology. An antibody was isolated that reacted with long term activated antigen-specific (tetanus toxoid) T lymphocytes originally isolated from blood lymphocytes. The cell lines were created Dr. Jim T. Kurnick's lab. Although the antibody did not block primary activation of T lymphocytes, it appeared late after activation with a number of lymphocytic stimuli,and was named "Act-1" because it was the first activation marker identified by this group of investigators. Dr. Andrew Lazarovits, a postdoctoral fellow in the laboratory, discovered the murine homologue of MLN0002,[8][9] chiefly published the original key papers, and up until the late 90's, coordinated, and led the studies for its development and application for Crohn's Disease and Ulcerative Colitis. Dr. Lynn Baird's group showed the antibody reacted with a single protein band of 63Kd, and Dr. Atul Bhan's group showed that it stained tissue lymphocytes but did not react with non-lymphoid tissues. Although Act-1 had limited efficacy in its ability to prevent kidney rejection in a sub-human primate transplantation model, Dr. Lazarovits continued to investigate the activities of Act-1 when he returned to Canada to become the Director of Transplantation at the University of Western Ontario.[9]

It was later determined that the Act-1 monoclonal antibody reacted with an alpha-4/beta-7 integrin that was subsequently shown to interact with a gut-associated addressin, MadCAM. Early work with Yacyshyn showed differential expression in inflammatory bowel disease (5). Dr. Lazarovits isolated the antibody to produce the murine homologue MLN002 which he licensed with the Massachusetts General Hospital to Millennium Pharmaceuticals of Boston for further development.[8] Scientists at LeukoSite realized the potential of this antibody to treat inflammatory bowel disease, and this company was eventually acquired by Millennium which took an exclusive license to the cell line from Massachusetts General Hospital. In vivo proof of concept ultimately led to the decision to humanize the antibody and move it into clinical trials as "Vedolizumab." In addition to its reactivity to gut-associated lymphoid tissues, Act-1 antibody also stains large numbers of lymphocytes in rheumatoid synovium, and has been shown by Dr. A. A. Ansari of Emory University to prevent or delay onset of AIDS in a monkey-model of Simian Immunodeficiency Virus-induced AIDS. Thus, reactivity with this antibody may show widespread applicability in inflammatory processes of diverse etiologies.

Approval status

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Takeda has filed a Marketing_Authorization_Application (MAA) in the European Union on March 7, 2013[10] and a Biologic_License_Application (BLA) with the U.S. Food and Drug Administration on June 21, 2013 for both Crohn's Disease and Ulcerative Colitis.[11] On September 4, 2013, Vedolizumab was given a Priority Review Status, which functions to expedite potential acceptance to market.[12]

On December 9, 2013, the Gastrointestinal Drugs Advisory Committee (GIDAC) & Drug Safety and Risk Management Advisory Committee (DSaRM) discussed the Vedolizumab application for approval for both UC and CD under the trade name Entyvio.[13] The voting went as follows: 1. Safety and efficacy data outweigh potential risks 21-0 2. In favour of UC treatment 21-0 3. In favour for CD treatment 20-1.[14][15] Although GIDAC/DSaRM were a non-binding advisory committee, their opinions as field experts represent one of the last steps towards drug acceptance.

On 20 March 2014, the Committee for Medicinal Products for Human Use (CHMP, the committee advising the European Commission) adopted a positive opinion, recommending the granting of a marketing authorization for Vedolizumab (brand name Entyvio).[16]

On 20 May 2014, vedolizumab (Entyvio) was approved by the FDA for treatment of both moderate-to-severe ulcerative colitis and moderate-to-severe Crohn's disease.[17] On May 27, 2014, Entyvio was approved for the treatment of both ulcerative colitis and Crohn's disease in the 28 European Union states as well as Norway, Iceland and Lichtenstein. On April 28, 2015 Health Canada approved Entyvio. [18]

Research

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Vedolizumab eventually completed a number of phase 3 clinical trials[19][20] for Crohn's Disease and Ulcerative Colitis (GEMINI I,[21] GEMINI II,[22] and GEMINI III[23]) that demonstrate that vedolizumab is an effective and well tolerated drug.[24][25] The results of the GEMINI 1 and GEMINI 2 randomized, placebo controlled multicenter trials of induction and maintenance therapy in Crohn's disease and ulcerative colitis have been published.[26][27] An additional clinical trial, GEMINI LTS (Long-term Safety), is still being run.[28]

References

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  1. ^ Insert footnote text here
  2. ^ a b Statement On A Nonproprietary Name Adopted By The USAN Council - Vedolizumab, American Medical Association.
  3. ^ Soler D, Chapman T, Yang LL, Wyant T, Egan R, Fedyk ER (September 2009). "The binding specificity and selective antagonism of vedolizumab, an anti-alpha4beta7 integrin therapeutic antibody in development for inflammatory bowel diseases". J. Pharmacol. Exp. Ther. 330 (3): 864–75. doi:10.1124/jpet.109.153973. PMID 19509315.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Fedyk ER, Wyant T, Yang LL, Csizmadia V, Burke K, Yang H, Kadambi VJ (November 2012). "Exclusive antagonism of the α4β7 integrin by vedolizumab confirms the gut-selectivity of this pathway in primates". Inflamm. Bowel Dis. 18 (11): 2107–19. doi:10.1002/ibd.22940. PMID 22419649.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ "DailyMed - LOVENOX- enoxaparin sodium injection". dailymed.nlm.nih.gov. Retrieved 2015-11-04.
  6. ^ a b Summary of the risk management plan (RMP) for Entyvio, EMA.
  7. ^ Entyvio prescribing information
  8. ^ a b Feagan B, Greenberg G, Wild G, Fedorak R, Pi Paré P, McDonald J, Cohen, A, Bitton A, Baker J, Dubé R, Landau S, Vandervoort M, Parikh A. (2008). "Treatment of Active Crohn's Disease With MLN0002, a Humanized Antibody to the α4β7 Integrin". Clinical Gastroenterology and Hepatology. 6 (12): 1370–77. doi:10.1016/j.cgh.2008.06.007. PMID 18829392.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  9. ^ a b Lazarovits AI, Moscicki RA, Kurnick JT, Camerini D, Bhan AK, Baird LG, Erikson M, Colvin RB (1984). "Lymphocyte activation antigens. I. A monoclonal antibody, anti-Act I, defines a new late lymphocyte activation antigen". J. Immunol. 133 (4): 1857–62. PMID 6088627.{{cite journal}}: CS1 maint: multiple names: authors list (link) Cite error: The named reference "pmid6088627" was defined multiple times with different content (see the help page).
  10. ^ "Takeda Submits Marketing Authorisation Application for Vedolizumab in Moderately to Severely Active Ulcerative Colitis and Crohn's Disease in the European Union". Press Release. Takeda Pharmaceutical Company Limited. 2013-03-08.
  11. ^ "Takeda Submits Vedolizumab BLA". Drug Discovery and Development. 2013-06-21. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  12. ^ "Takeda's New Investigational Drug Vedolizumab is Granted Priority Review Status by U.S. Food and Drug Administration for Ulcerative Colitis". Press Release. Takeda Pharmaceutical Company Limited. 2013-09-04.
  13. ^ http://www.fdalive.com/results.cfm
  14. ^ http://www.takeda.com/news/files/20131210_04_en.pdf
  15. ^ https://research.tdwaterhouse.ca/research/public/Markets/NewsArticle/100-343p7866-1
  16. ^ http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/002782/smops/Positive/human_smop_000663.jsp&mid=WC0b01ac058001d127
  17. ^ http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm398065.htm
  18. ^ http://www.hc-sc.gc.ca/dhp-mps/prodpharma/sbd-smd/drug-med/sbd_smd_2015_entyvio_169414-eng.php
  19. ^ "Vedolizumab". List Results. ClinicalTrials.gov.
  20. ^ "Data Published in the New England Journal of Medicine for Vedolizumab, an Investigational New Drug from Takeda for Moderately to Severely Active Ulcerative Colitis and Crohn's Disease". Press Release. Takeda Pharmaceutical Company Limited. 2013-08-23.
  21. ^ Clinical trial number NCT00783718 at ClinicalTrials.gov
  22. ^ Clinical trial number NCT00783692 at ClinicalTrials.gov
  23. ^ Clinical trial number NCT01224171 at ClinicalTrials.gov
  24. ^ McLean LP, Shea-Donohue T, Cross RK (September 2012). "Vedolizumab for the treatment of ulcerative colitis and Crohn's disease". Immunotherapy. 4 (9): 883–98. doi:10.2217/imt.12.85. PMC 3557917. PMID 23046232.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  25. ^ Mosli MH, Feagan BG (March 2013). "Vedolizumab for Crohn's disease". Expert Opin Biol Ther. 13 (3): 455–63. doi:10.1517/14712598.2013.770835. PMID 23394379.
  26. ^ Feagan BG, Rutgeerts P, Sands BE, Hanauer S, Colombel JF, Sandborn WJ, Van Assche G, Axler J, Kim HJ, Danese S, Fox I, Milch C, Sankoh S, Wyant T, Xu J, Parikh A (August 2013). "Vedolizumab as induction and maintenance therapy for ulcerative colitis". N. Engl. J. Med. 369 (8): 699–710. doi:10.1056/NEJMoa1215734. PMID 23964932.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  27. ^ Sandborn WJ, Feagan BG, Rutgeerts P, Hanauer S, Colombel JF, Sands BE, Lukas M, Fedorak RN, Lee S, Bressler B, Fox I, Rosario M, Sankoh S, Xu J, Stephens K, Milch C, Parikh A (August 2013). "Vedolizumab as induction and maintenance therapy for Crohn's disease". N. Engl. J. Med. 369 (8): 711–21. doi:10.1056/NEJMoa1215739. PMID 23964933.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  28. ^ Clinical trial number NCT00790933 at ClinicalTrials.gov

(5) Yacyshyn BR, Lazarovits A, Tsai V, Matejko K, Crohns disease, ulcerative colitis and normal intestinal lymphocytes express integrins in a dissimilar pattern. Gastroenterology 1994 (107), 1364-1371.

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