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
Hauptverfasser: Zhang, Xin, Lam, Eric Chen Quin, Seger, Mary E., Coutant, David, Chua, Laiyi, Tan, Lai Hock, Soon, Danny, Linnebjerg, Helle
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container_end_page 563
container_issue 6
container_start_page 556
container_title Clinical pharmacology in drug development
container_volume 6
creator Zhang, Xin
Lam, Eric Chen Quin
Seger, Mary E.
Coutant, David
Chua, Laiyi
Tan, Lai Hock
Soon, Danny
Linnebjerg, Helle
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 &amp; dosage ; Hypoglycemic Agents - pharmacokinetics ; Hypoglycemic Agents - pharmacology ; Insulin ; Insulin Glargine - administration &amp; dosage ; Insulin Glargine - analogs &amp; 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 &amp; dosage</subject><subject>Hypoglycemic Agents - pharmacokinetics</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Insulin</subject><subject>Insulin Glargine - administration &amp; dosage</subject><subject>Insulin Glargine - analogs &amp; 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 &amp; dosage</topic><topic>Hypoglycemic Agents - pharmacokinetics</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Insulin</topic><topic>Insulin Glargine - administration &amp; dosage</topic><topic>Insulin Glargine - analogs &amp; 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 &amp; 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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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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