Conference Report: Bio-International 2005
This is a summary report of the International Pharmaceutical Federation/Board of Pharmaceutical Sciences (FIP/BPS) international conference, Bio-International 2005, which was held October 24–26, 2005 at the Royal Pharmaceutical Society, in London, UK. Bioequivalence (BE) issues related to multisourc...
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Veröffentlicht in: | Journal of pharmaceutical sciences 2007-04, Vol.96 (4), p.747-754 |
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creator | Midha, Kamal K. Shah, Vinod P. Singh, Gur Jai Pal Patnaik, Rabi |
description | This is a summary report of the International Pharmaceutical Federation/Board of Pharmaceutical Sciences (FIP/BPS) international conference, Bio-International 2005, which was held October 24–26, 2005 at the Royal Pharmaceutical Society, in London, UK. Bioequivalence (BE) issues related to multisource locally delivered topical dosage forms, oral inhalation drug products, highly variable drug products (HVDP), and endogenously occurring drugs were discussed. The conference also focused on alternate approaches to assess BE for some of these drug products. Pharmacokinetic (PK) approaches like, dermatopharmacokinetics (DPK) for dermatological topical dosage forms, scaled average BE (s-ABE) where within-subject variability is considered for estimation of 90% confidence intervals to document BE for highly variable drugs (HVD) were recommended. In addition, issues and difficulties related to the BE assessment of oral inhalation products, role, and appropriateness of metabolites in BE assessment, importance of base line correction in BE assessment of endogenously occurring drugs, and waiver of BE study requirements for certain drugs based on a Biopharmaceutics Classification System (BCS), were also discussed. |
doi_str_mv | 10.1002/jps.20786 |
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In addition, issues and difficulties related to the BE assessment of oral inhalation products, role, and appropriateness of metabolites in BE assessment, importance of base line correction in BE assessment of endogenously occurring drugs, and waiver of BE study requirements for certain drugs based on a Biopharmaceutics Classification System (BCS), were also discussed.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.20786</identifier><identifier>PMID: 17094144</identifier><language>eng</language><publisher>Hoboken: Elsevier Inc</publisher><subject>Administration, Inhalation ; Administration, Topical ; bioavailability ; bioequivalence ; Biological Availability ; Biopharmaceutics - classification ; Biopharmaceutics Classification System ; Humans ; regulatory science ; Therapeutic Equivalency ; transdermal</subject><ispartof>Journal of pharmaceutical sciences, 2007-04, Vol.96 (4), p.747-754</ispartof><rights>2007 Wiley‐Liss, Inc.</rights><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>(c) 2006 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4056-65a4364f934392c02aac2860ccac8bfc2ab53d6af9d5617e020ff99ce94371fe3</citedby><cites>FETCH-LOGICAL-c4056-65a4364f934392c02aac2860ccac8bfc2ab53d6af9d5617e020ff99ce94371fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.20786$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.20786$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17094144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Midha, Kamal K.</creatorcontrib><creatorcontrib>Shah, Vinod P.</creatorcontrib><creatorcontrib>Singh, Gur Jai Pal</creatorcontrib><creatorcontrib>Patnaik, Rabi</creatorcontrib><title>Conference Report: Bio-International 2005</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>This is a summary report of the International Pharmaceutical Federation/Board of Pharmaceutical Sciences (FIP/BPS) international conference, Bio-International 2005, which was held October 24–26, 2005 at the Royal Pharmaceutical Society, in London, UK. Bioequivalence (BE) issues related to multisource locally delivered topical dosage forms, oral inhalation drug products, highly variable drug products (HVDP), and endogenously occurring drugs were discussed. The conference also focused on alternate approaches to assess BE for some of these drug products. Pharmacokinetic (PK) approaches like, dermatopharmacokinetics (DPK) for dermatological topical dosage forms, scaled average BE (s-ABE) where within-subject variability is considered for estimation of 90% confidence intervals to document BE for highly variable drugs (HVD) were recommended. In addition, issues and difficulties related to the BE assessment of oral inhalation products, role, and appropriateness of metabolites in BE assessment, importance of base line correction in BE assessment of endogenously occurring drugs, and waiver of BE study requirements for certain drugs based on a Biopharmaceutics Classification System (BCS), were also discussed.</description><subject>Administration, Inhalation</subject><subject>Administration, Topical</subject><subject>bioavailability</subject><subject>bioequivalence</subject><subject>Biological Availability</subject><subject>Biopharmaceutics - classification</subject><subject>Biopharmaceutics Classification System</subject><subject>Humans</subject><subject>regulatory science</subject><subject>Therapeutic Equivalency</subject><subject>transdermal</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1PGzEQhq0KVELogT-AckLKYWH8uXFvJSohKC39QhwtxzuWTDe7W3vDx79nw4ZygdMc5nlfzTyEHFI4oQDs9LZJJwzyifpABlQyyBTQfIcMuh3LuBR6j-yndAsACqT8SPZoDlpQIQZkPK0rjxErh6Nf2NSx_Tw6C3U2r1qMlW1DXdlyxADkAdn1tkz4aTuH5Pr865_pRba4ms2nXxaZEyBVpqQVXAmvueCaOWDWOjZR4Jx1k6V3zC4lL5T1upCK5ggMvNfaoRY8px75kBz3vU2s_60xtWYVksOytBXW62Ty7qkO1R047kEX65QietPEsLLx0VAwGy-m82KevXTs0bZ0vVxh8UpuRXTAaQ_chxIf328ylz9-v1RmfSKkFh_-J2z8a1TOc2luvs8M_ORCfoOF2fC857GTdxcwmuTCxnsRIrrWFHV44_AnfZOKug</recordid><startdate>200704</startdate><enddate>200704</enddate><creator>Midha, Kamal K.</creator><creator>Shah, Vinod P.</creator><creator>Singh, Gur Jai Pal</creator><creator>Patnaik, Rabi</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200704</creationdate><title>Conference Report: Bio-International 2005</title><author>Midha, Kamal K. ; Shah, Vinod P. ; Singh, Gur Jai Pal ; Patnaik, Rabi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4056-65a4364f934392c02aac2860ccac8bfc2ab53d6af9d5617e020ff99ce94371fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Administration, Inhalation</topic><topic>Administration, Topical</topic><topic>bioavailability</topic><topic>bioequivalence</topic><topic>Biological Availability</topic><topic>Biopharmaceutics - classification</topic><topic>Biopharmaceutics Classification System</topic><topic>Humans</topic><topic>regulatory science</topic><topic>Therapeutic Equivalency</topic><topic>transdermal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Midha, Kamal K.</creatorcontrib><creatorcontrib>Shah, Vinod P.</creatorcontrib><creatorcontrib>Singh, Gur Jai Pal</creatorcontrib><creatorcontrib>Patnaik, Rabi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Midha, Kamal K.</au><au>Shah, Vinod P.</au><au>Singh, Gur Jai Pal</au><au>Patnaik, Rabi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conference Report: Bio-International 2005</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>2007-04</date><risdate>2007</risdate><volume>96</volume><issue>4</issue><spage>747</spage><epage>754</epage><pages>747-754</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><abstract>This is a summary report of the International Pharmaceutical Federation/Board of Pharmaceutical Sciences (FIP/BPS) international conference, Bio-International 2005, which was held October 24–26, 2005 at the Royal Pharmaceutical Society, in London, UK. Bioequivalence (BE) issues related to multisource locally delivered topical dosage forms, oral inhalation drug products, highly variable drug products (HVDP), and endogenously occurring drugs were discussed. The conference also focused on alternate approaches to assess BE for some of these drug products. Pharmacokinetic (PK) approaches like, dermatopharmacokinetics (DPK) for dermatological topical dosage forms, scaled average BE (s-ABE) where within-subject variability is considered for estimation of 90% confidence intervals to document BE for highly variable drugs (HVD) were recommended. In addition, issues and difficulties related to the BE assessment of oral inhalation products, role, and appropriateness of metabolites in BE assessment, importance of base line correction in BE assessment of endogenously occurring drugs, and waiver of BE study requirements for certain drugs based on a Biopharmaceutics Classification System (BCS), were also discussed.</abstract><cop>Hoboken</cop><pub>Elsevier Inc</pub><pmid>17094144</pmid><doi>10.1002/jps.20786</doi><tpages>8</tpages></addata></record> |
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subjects | Administration, Inhalation Administration, Topical bioavailability bioequivalence Biological Availability Biopharmaceutics - classification Biopharmaceutics Classification System Humans regulatory science Therapeutic Equivalency transdermal |
title | Conference Report: Bio-International 2005 |
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