LY2963016 Insulin Glargine and Insulin Glargine (Lantus) Produce Comparable Pharmacokinetics and Pharmacodynamics at Two Dose Levels
LY2963016 (LY IGlar) and Lantus (IGlar) are insulin glargine products with identical amino acid sequences. This was a phase 1 single‐site, randomized, subject‐ and investigator‐blinded, 4‐treatment, 4‐period crossover study to compare the pharmacokinetic (PK) and pharmacodynamic (PD) properties of L...
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Veröffentlicht in: | Clinical pharmacology in drug development 2017-11, Vol.6 (6), p.556-563 |
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description | LY2963016 (LY IGlar) and Lantus (IGlar) are insulin glargine products with identical amino acid sequences. This was a phase 1 single‐site, randomized, subject‐ and investigator‐blinded, 4‐treatment, 4‐period crossover study to compare the pharmacokinetic (PK) and pharmacodynamic (PD) properties of LY IGlar and IGlar at 2 different doses. Fasted healthy subjects were randomly assigned to receive 2 single doses of LY IGlar and IGlar (0.3 and 0.6 U/kg for each product). Blood samples were collected up to 24 hours postdose to assess PK, and a euglycemic clamp lasting up to 24 hours postdose was conducted to assess PD. Twenty‐four healthy subjects aged 23 to 52 years participated in the study. The primary PK parameters (area under the concentration versus time curve from 0 to 24 hours [AUC0–24] and maximum observed drug concentration [Cmax]) and PD parameters (total amount of glucose infused during the clamp [Gtot] and maximum glucose infusion rate [Rmax]) were not statistically different between LY IGlar and IGlar at either dose. No safety concerns were noted with either drug. The study demonstrated that the PK and PD parameters for LY IGlar and IGlar were comparable following single doses at both 0.3 and 0.6 U/kg. |
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This was a phase 1 single‐site, randomized, subject‐ and investigator‐blinded, 4‐treatment, 4‐period crossover study to compare the pharmacokinetic (PK) and pharmacodynamic (PD) properties of LY IGlar and IGlar at 2 different doses. Fasted healthy subjects were randomly assigned to receive 2 single doses of LY IGlar and IGlar (0.3 and 0.6 U/kg for each product). Blood samples were collected up to 24 hours postdose to assess PK, and a euglycemic clamp lasting up to 24 hours postdose was conducted to assess PD. Twenty‐four healthy subjects aged 23 to 52 years participated in the study. The primary PK parameters (area under the concentration versus time curve from 0 to 24 hours [AUC0–24] and maximum observed drug concentration [Cmax]) and PD parameters (total amount of glucose infused during the clamp [Gtot] and maximum glucose infusion rate [Rmax]) were not statistically different between LY IGlar and IGlar at either dose. No safety concerns were noted with either drug. The study demonstrated that the PK and PD parameters for LY IGlar and IGlar were comparable following single doses at both 0.3 and 0.6 U/kg.</description><identifier>ISSN: 2160-763X</identifier><identifier>EISSN: 2160-7648</identifier><identifier>DOI: 10.1002/cpdd.392</identifier><identifier>PMID: 28940840</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Area Under Curve ; biosimilar insulin ; Cross-Over Studies ; Dose-Response Relationship, Drug ; Double-Blind Method ; Drug dosages ; euglycemic clamp ; Female ; glucodynamics ; Glucose ; Glucose Clamp Technique ; Humans ; Hypoglycemic Agents - administration & dosage ; Hypoglycemic Agents - pharmacokinetics ; Hypoglycemic Agents - pharmacology ; Insulin ; Insulin Glargine - administration & dosage ; Insulin Glargine - analogs & derivatives ; Insulin Glargine - pharmacokinetics ; Insulin Glargine - pharmacology ; Male ; Middle Aged ; Pharmacodynamics ; Pharmacokinetics ; Pharmacology ; type 1 diabetes mellitus ; type 2 diabetes mellitus ; Young Adult</subject><ispartof>Clinical pharmacology in drug development, 2017-11, Vol.6 (6), p.556-563</ispartof><rights>2017, The American College of Clinical Pharmacology</rights><rights>2017, The American College of Clinical Pharmacology.</rights><rights>American College of Clinical Pharmacology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3492-dc6af460edc9bcc56de0ad43be319a18389a777264c31b6b412ab24bbadc12a13</citedby><cites>FETCH-LOGICAL-c3492-dc6af460edc9bcc56de0ad43be319a18389a777264c31b6b412ab24bbadc12a13</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%2Fcpdd.392$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcpdd.392$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27913,27914,45563,45564</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28940840$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Xin</creatorcontrib><creatorcontrib>Lam, Eric Chen Quin</creatorcontrib><creatorcontrib>Seger, Mary E.</creatorcontrib><creatorcontrib>Coutant, David</creatorcontrib><creatorcontrib>Chua, Laiyi</creatorcontrib><creatorcontrib>Tan, Lai Hock</creatorcontrib><creatorcontrib>Soon, Danny</creatorcontrib><creatorcontrib>Linnebjerg, Helle</creatorcontrib><title>LY2963016 Insulin Glargine and Insulin Glargine (Lantus) Produce Comparable Pharmacokinetics and Pharmacodynamics at Two Dose Levels</title><title>Clinical pharmacology in drug development</title><addtitle>Clin Pharmacol Drug Dev</addtitle><description>LY2963016 (LY IGlar) and Lantus (IGlar) are insulin glargine products with identical amino acid sequences. This was a phase 1 single‐site, randomized, subject‐ and investigator‐blinded, 4‐treatment, 4‐period crossover study to compare the pharmacokinetic (PK) and pharmacodynamic (PD) properties of LY IGlar and IGlar at 2 different doses. Fasted healthy subjects were randomly assigned to receive 2 single doses of LY IGlar and IGlar (0.3 and 0.6 U/kg for each product). Blood samples were collected up to 24 hours postdose to assess PK, and a euglycemic clamp lasting up to 24 hours postdose was conducted to assess PD. Twenty‐four healthy subjects aged 23 to 52 years participated in the study. The primary PK parameters (area under the concentration versus time curve from 0 to 24 hours [AUC0–24] and maximum observed drug concentration [Cmax]) and PD parameters (total amount of glucose infused during the clamp [Gtot] and maximum glucose infusion rate [Rmax]) were not statistically different between LY IGlar and IGlar at either dose. No safety concerns were noted with either drug. The study demonstrated that the PK and PD parameters for LY IGlar and IGlar were comparable following single doses at both 0.3 and 0.6 U/kg.</description><subject>Adult</subject><subject>Area Under Curve</subject><subject>biosimilar insulin</subject><subject>Cross-Over Studies</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Drug dosages</subject><subject>euglycemic clamp</subject><subject>Female</subject><subject>glucodynamics</subject><subject>Glucose</subject><subject>Glucose Clamp Technique</subject><subject>Humans</subject><subject>Hypoglycemic Agents - administration & dosage</subject><subject>Hypoglycemic Agents - pharmacokinetics</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Insulin</subject><subject>Insulin Glargine - administration & dosage</subject><subject>Insulin Glargine - analogs & derivatives</subject><subject>Insulin Glargine - pharmacokinetics</subject><subject>Insulin Glargine - pharmacology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pharmacodynamics</subject><subject>Pharmacokinetics</subject><subject>Pharmacology</subject><subject>type 1 diabetes mellitus</subject><subject>type 2 diabetes mellitus</subject><subject>Young Adult</subject><issn>2160-763X</issn><issn>2160-7648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctKxDAUhoMoKir4BBJwo4tqbqbNUma8QcFZKOiqnFxGO7bNmEyV2fvgZryMoJjNOfx8fITzI7RLyRElhB2bqbVHXLEVtMmoJFkuRbG63PndBtqJcULSk4RSKtbRBiuUIIUgm-itvGdKckIlvupi39QdvmggPNSdw9DZv-FBCd2sj4d4FLztjcMD304hgG4cHj1CaMH4pwTOahM_DN-hnXfQfoQzfPPq8dBHh0v34pq4jdbG0ES38zW30O352c3gMiuvL64Gp2VmuFAss0bCWEjirFHamBNpHQEruHacKqAFLxTkec6kMJxqqQVloJnQGqxJK-Vb6ODTOw3-uXdxVrV1NK5poHO-jxVVguXpTEoldP8XOvF96NLvEiUZT5en5Edogo8xuHE1DXULYV5RUi3KqRblVKmchO59CXvdOrsEv6tIQPYJvNaNm_8rqgaj4XAhfAer-5f6</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Zhang, Xin</creator><creator>Lam, Eric Chen Quin</creator><creator>Seger, Mary E.</creator><creator>Coutant, David</creator><creator>Chua, Laiyi</creator><creator>Tan, Lai Hock</creator><creator>Soon, Danny</creator><creator>Linnebjerg, Helle</creator><general>Wiley Subscription Services, Inc</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>201711</creationdate><title>LY2963016 Insulin Glargine and Insulin Glargine (Lantus) Produce Comparable Pharmacokinetics and Pharmacodynamics at Two Dose Levels</title><author>Zhang, Xin ; Lam, Eric Chen Quin ; Seger, Mary E. ; Coutant, David ; Chua, Laiyi ; Tan, Lai Hock ; Soon, Danny ; Linnebjerg, Helle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3492-dc6af460edc9bcc56de0ad43be319a18389a777264c31b6b412ab24bbadc12a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Area Under Curve</topic><topic>biosimilar insulin</topic><topic>Cross-Over Studies</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Drug dosages</topic><topic>euglycemic clamp</topic><topic>Female</topic><topic>glucodynamics</topic><topic>Glucose</topic><topic>Glucose Clamp Technique</topic><topic>Humans</topic><topic>Hypoglycemic Agents - administration & dosage</topic><topic>Hypoglycemic Agents - pharmacokinetics</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Insulin</topic><topic>Insulin Glargine - administration & dosage</topic><topic>Insulin Glargine - analogs & derivatives</topic><topic>Insulin Glargine - pharmacokinetics</topic><topic>Insulin Glargine - pharmacology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pharmacodynamics</topic><topic>Pharmacokinetics</topic><topic>Pharmacology</topic><topic>type 1 diabetes mellitus</topic><topic>type 2 diabetes mellitus</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xin</creatorcontrib><creatorcontrib>Lam, Eric Chen Quin</creatorcontrib><creatorcontrib>Seger, Mary E.</creatorcontrib><creatorcontrib>Coutant, David</creatorcontrib><creatorcontrib>Chua, Laiyi</creatorcontrib><creatorcontrib>Tan, Lai Hock</creatorcontrib><creatorcontrib>Soon, Danny</creatorcontrib><creatorcontrib>Linnebjerg, Helle</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical pharmacology in drug development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xin</au><au>Lam, Eric Chen Quin</au><au>Seger, Mary E.</au><au>Coutant, David</au><au>Chua, Laiyi</au><au>Tan, Lai Hock</au><au>Soon, Danny</au><au>Linnebjerg, Helle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LY2963016 Insulin Glargine and Insulin Glargine (Lantus) Produce Comparable Pharmacokinetics and Pharmacodynamics at Two Dose Levels</atitle><jtitle>Clinical pharmacology in drug development</jtitle><addtitle>Clin Pharmacol Drug Dev</addtitle><date>2017-11</date><risdate>2017</risdate><volume>6</volume><issue>6</issue><spage>556</spage><epage>563</epage><pages>556-563</pages><issn>2160-763X</issn><eissn>2160-7648</eissn><abstract>LY2963016 (LY IGlar) and Lantus (IGlar) are insulin glargine products with identical amino acid sequences. This was a phase 1 single‐site, randomized, subject‐ and investigator‐blinded, 4‐treatment, 4‐period crossover study to compare the pharmacokinetic (PK) and pharmacodynamic (PD) properties of LY IGlar and IGlar at 2 different doses. Fasted healthy subjects were randomly assigned to receive 2 single doses of LY IGlar and IGlar (0.3 and 0.6 U/kg for each product). Blood samples were collected up to 24 hours postdose to assess PK, and a euglycemic clamp lasting up to 24 hours postdose was conducted to assess PD. Twenty‐four healthy subjects aged 23 to 52 years participated in the study. The primary PK parameters (area under the concentration versus time curve from 0 to 24 hours [AUC0–24] and maximum observed drug concentration [Cmax]) and PD parameters (total amount of glucose infused during the clamp [Gtot] and maximum glucose infusion rate [Rmax]) were not statistically different between LY IGlar and IGlar at either dose. No safety concerns were noted with either drug. The study demonstrated that the PK and PD parameters for LY IGlar and IGlar were comparable following single doses at both 0.3 and 0.6 U/kg.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28940840</pmid><doi>10.1002/cpdd.392</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Area Under Curve biosimilar insulin Cross-Over Studies Dose-Response Relationship, Drug Double-Blind Method Drug dosages euglycemic clamp Female glucodynamics Glucose Glucose Clamp Technique Humans Hypoglycemic Agents - administration & dosage Hypoglycemic Agents - pharmacokinetics Hypoglycemic Agents - pharmacology Insulin Insulin Glargine - administration & dosage Insulin Glargine - analogs & derivatives Insulin Glargine - pharmacokinetics Insulin Glargine - pharmacology Male Middle Aged Pharmacodynamics Pharmacokinetics Pharmacology type 1 diabetes mellitus type 2 diabetes mellitus Young Adult |
title | LY2963016 Insulin Glargine and Insulin Glargine (Lantus) Produce Comparable Pharmacokinetics and Pharmacodynamics at Two Dose Levels |
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