Difference between revisions of "Apligraf"

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Apligraf is a synthetic skin created from harvested foreskins.<ref>{{REFwebQuote
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'''Apligraf''' is a synthetic [[skin]] created from harvested foreskins.<ref>{{REFweb
  | quote=Human keratinocytes and fibroblasts are derived from neonatal foreskins
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  |quote=Human keratinocytes and fibroblasts are derived from neonatal foreskins
  | last=
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  |url=http://www.apligraf.com/professional/what_is_apligraf/how_is_it_made/
  | first=
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  |title=Apligraf: How Is It Made?
  | publisher=Organogenesis
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  |last=
  | year=
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  |first=
  | urltitle=Apligraf: How Is It Made?
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  |publisher=Organogenesis
  | url=http://www.apligraf.com/professional/what_is_apligraf/how_is_it_made/
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  |date=
  | accessdate=2011-03-06
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  |accessdate=2011-03-06
}}</ref> It is [[FDA]] approved,<ref>{{REFwebQuote
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}}</ref> It is [[FDA]] approved,<ref>{{REFweb
  | quote=Apligraf® is the first bio-engineered cell based product to receive FDA approval (in 1998).
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  |quote=Apligraf® is the first bio-engineered cell based product to receive FDA approval (in 1998).
  | last=
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  |url=http://www.organogenesis.com/products/bioactive_woundhealing/apligraf.html
  | first=
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  |title=Apligraf
  | publisher=Organogenesis
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  |last=
  | year=
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  |first=
  | urltitle=Apligraf
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  |publisher=Organogenesis
  | url=http://www.organogenesis.com/products/bioactive_woundhealing/apligraf.html
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  |date=
  | accessdate=2011-03-06
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  |accessdate=2011-03-06
}}</ref> and it is made and sold by [[Organogenesis]], which a corporation based in Canton, MA. Novartis Pharmaceuticals Corp. has global marketing rights to Apligraf.
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}}</ref> and it is made and sold by [[Organogenesis]], a corporation based in Canton, MA. Novartis Pharmaceuticals Corp. has global marketing rights to Apligraf.
  
 
== Apligraph Oral ==
 
== Apligraph Oral ==
  
 
Organogenesis is presently seeking FDA approval for Apligraph Oral, a foreskin-derived product for the "treatment of surgically treated gingival and alveolar mucosal surface defects in adults."<ref>{{REFnews
 
Organogenesis is presently seeking FDA approval for Apligraph Oral, a foreskin-derived product for the "treatment of surgically treated gingival and alveolar mucosal surface defects in adults."<ref>{{REFnews
  | last=
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  |last=
  | first=
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  |first=
| coauthors=
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  |url=http://www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMaterials/BloodVaccinesandOtherBiologics/CellularTissueandGeneTherapiesAdvisoryCommittee/UCM284112.pdf
  | url=http://www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMaterials/BloodVaccinesandOtherBiologics/CellularTissueandGeneTherapiesAdvisoryCommittee/UCM284112.pdf
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  |title=November 17, 2011: Cellular, Tissue and Gene Therapies Advisory Committee Meeting: Transcript
  | title=November 17, 2011: Cellular, Tissue and Gene Therapies Advisory Committee Meeting: Transcript
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  |date=2011-11-17
  | date=November 2011
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  |publisher=FDA
  | publisher=FDA
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  |quote=
  | quote=
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  |accessdate=2011-12-20
  | accessdate=2011-12-20
 
 
}}</ref>
 
}}</ref>
 
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Sponsor slides: http://www.fda.gov/downloads/advisorycommittees/committeesmeetingmaterials/bloodvaccinesandotherbiologics/cellulartissueandgenetherapiesadvisorycommittee/ucm284480.pdf
 
 
 
 
{{REF}}
 
{{REF}}
  
[[Category:Foreskin Products]]
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[[Category:Foreskin product]]
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Latest revision as of 16:56, 27 December 2021

Apligraf is a synthetic skin created from harvested foreskins.[1] It is FDA approved,[2] and it is made and sold by Organogenesis, a corporation based in Canton, MA. Novartis Pharmaceuticals Corp. has global marketing rights to Apligraf.

Apligraph Oral

Organogenesis is presently seeking FDA approval for Apligraph Oral, a foreskin-derived product for the "treatment of surgically treated gingival and alveolar mucosal surface defects in adults."[3]

References

  1. REFweb Apligraf: How Is It Made?, Organogenesis. Retrieved 6 March 2011.
    Quote: Human keratinocytes and fibroblasts are derived from neonatal foreskins
  2. REFweb Apligraf, Organogenesis. Retrieved 6 March 2011.
    Quote: Apligraf® is the first bio-engineered cell based product to receive FDA approval (in 1998).
  3. REFnews (17 November 2011)."November 17, 2011: Cellular, Tissue and Gene Therapies Advisory Committee Meeting: Transcript", FDA. Retrieved 20 December 2011.