Pharmacokinetic Similarity of ABP 654, an Ustekinumab Biosimilar Candidate: Results from a Randomized, Double‐blind Study in Healthy Subjects

ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin‐12 and interleukin‐23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease...

Full description

Saved in:
Bibliographic Details
Published inClinical pharmacology in drug development Vol. 12; no. 9; pp. 863 - 873
Main Authors Chow, Vincent, Mytych, Daniel T., Das, Shyamal, Franklin, Janet
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.09.2023
Subjects
Online AccessGet full text

Cover

Loading…
Abstract ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin‐12 and interleukin‐23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double‐blinded, single‐dose, 3‐arm, parallel‐group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non‐Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration‐time curve from time 0 extrapolated to infinity (AUCinf) and maximum observed serum concentration (Cmax) being contained within the prespecified margin of 0.8–1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.
AbstractList ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin‐12 and interleukin‐23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double‐blinded, single‐dose, 3‐arm, parallel‐group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non‐Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration‐time curve from time 0 extrapolated to infinity (AUCinf) and maximum observed serum concentration (Cmax) being contained within the prespecified margin of 0.8–1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.
ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin-12 and interleukin-23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double-blinded, single-dose, 3-arm, parallel-group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non-Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration-time curve from time 0 extrapolated to infinity (AUCinf ) and maximum observed serum concentration (Cmax ) being contained within the prespecified margin of 0.8-1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin-12 and interleukin-23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double-blinded, single-dose, 3-arm, parallel-group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non-Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration-time curve from time 0 extrapolated to infinity (AUCinf ) and maximum observed serum concentration (Cmax ) being contained within the prespecified margin of 0.8-1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.
ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin‐12 and interleukin‐23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double‐blinded, single‐dose, 3‐arm, parallel‐group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non‐Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration‐time curve from time 0 extrapolated to infinity (AUC inf ) and maximum observed serum concentration (C max ) being contained within the prespecified margin of 0.8–1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.
ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin-12 and interleukin-23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double-blinded, single-dose, 3-arm, parallel-group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non-Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration-time curve from time 0 extrapolated to infinity (AUC ) and maximum observed serum concentration (C ) being contained within the prespecified margin of 0.8-1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.
ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin‐12 and interleukin‐23. Ustekinumab RP is used for the treatment of chronic inflammatory conditions, including some forms of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis. A randomized, double‐blinded, single‐dose, 3‐arm, parallel‐group study was conducted to assess the pharmacokinetic (PK) similarity of ABP 654 with ustekinumab RP sourced from the United States (US) and the European Union (EU); the PK similarity of ustekinumab US versus ustekinumab EU; and the comparative safety, tolerability, and immunogenicity of all 3 products. A total of 238 healthy subjects were randomized 1:1:1 and stratified by gender and ethnicity (Japanese versus non‐Japanese) to receive a single 90 mg subcutaneous injection of ABP 654 or ustekinumab US or ustekinumab EU. PK similarity was established based on 90% confidence intervals (CIs) for the primary endpoints of area under the concentration‐time curve from time 0 extrapolated to infinity (AUCinf) and maximum observed serum concentration (Cmax) being contained within the prespecified margin of 0.8–1.25. No clinically meaningful differences in immunogenicity were found among the 3 products. Adverse events were similar between treatment groups and consistent with the safety profile of ustekinumab RP. Results indicate that ABP 654, ustekinumab US and ustekinumab EU share similar PK and safety profiles.
Author Mytych, Daniel T.
Das, Shyamal
Franklin, Janet
Chow, Vincent
Author_xml – sequence: 1
  givenname: Vincent
  surname: Chow
  fullname: Chow, Vincent
  organization: Amgen Inc
– sequence: 2
  givenname: Daniel T.
  surname: Mytych
  fullname: Mytych, Daniel T.
  organization: Amgen Inc
– sequence: 3
  givenname: Shyamal
  surname: Das
  fullname: Das, Shyamal
  organization: Amgen Inc
– sequence: 4
  givenname: Janet
  surname: Franklin
  fullname: Franklin, Janet
  email: jfrankli@amgen.com
  organization: Amgen Inc
BackLink https://www.ncbi.nlm.nih.gov/pubmed/37415567$$D View this record in MEDLINE/PubMed
BookMark eNp90d1qFDEUB_AgFVtrL3wBCXij0G3zNZmZ3rW7aoWCS9eCd0MyOUOzZpI1ySDjlW-gz-iTOOvWXhQ0NydwfucQ8n-K9nzwgNBzSk4oIey03RhzQjmhj9ABo5LMSimqvfs7_7SPjlJak-lIQikVT9A-LwUtClkeoB_LWxV71YbP1kO2LV7Z3joVbR5x6PD5xRLLQhxj5fFNyjCpoVcaX9iQdhDPlTfWqAxn-BrS4HLCXQw9Vvh66oTefgNzjBdh0A5-ff-pnfUGr_JgRmw9vgTl8u2IV4NeQ5vTM_S4Uy7B0V09RDdv33ycX86uPrx7Pz-_mrW8quhMEAptSStumCllJyqta0qk5IWWBUgqqNSGVUKDZFAwbWojSGXqrgNl6kLzQ_Rqt3cTw5cBUm56m1pwTnkIQ2pYxQtWUV6XE335gK7DEP30ukkVteCMETKpF3dq0D2YZhNtr-LY_P3qCbzegTaGlCJ094SSZptks02y2SY52dMHtrVZZRt8jsq6_018tQ7Gf69u5svF4s_Eb3OUr2w
CitedBy_id crossref_primary_10_1016_j_bpg_2025_101992
crossref_primary_10_1007_s40268_023_00441_7
crossref_primary_10_1002_cpdd_1473
crossref_primary_10_1177_24755303231212154
crossref_primary_10_1016_j_jaad_2024_04_045
crossref_primary_10_1002_ueg2_12682
crossref_primary_10_1016_j_ejps_2024_106807
crossref_primary_10_3390_biologics4040025
crossref_primary_10_1093_bjd_ljae402
crossref_primary_10_1093_bjd_ljae468
crossref_primary_10_2147_JIR_S478529
crossref_primary_10_3390_jcm12196350
Cites_doi 10.1016/S0140-6736(08)60725-4
10.1517/14712591003724670
10.1038/nm.3895
10.1007/s40268-023-00441-7
10.1136/annrheumdis-2015-208914
10.1093/ecco-jcc/jjac030
10.1038/nbt.1651
10.1007/s40259-017-0218-5
10.3390/biom9090410
10.1007/s40261-013-0072-2
10.1016/0264-410X(95)00189-8
10.4161/mabs.3.6.17815
10.1093/ecco-jcc/jjz110
10.1016/S0140-6736(13)60594-2
10.1016/S0140-6736(08)60726-6
10.1016/j.jpba.2008.09.020
10.21037/tlcr-20-601
10.4161/mabs.32114
10.1002/eji.200526146
10.1056/NEJMoa1602773
10.1111/bjd.16504
10.1136/ard.2008.092833
10.1007/s40265-020-01256-5
10.1007/s40273-018-0618-5
10.1093/ibd/izab334
10.3389/fphar.2019.00279
10.1023/B:PHAM.0000003390.51761.3d
10.1016/j.vaccine.2009.03.019
10.1136/annrheumdis-2013-204655
10.1111/apt.16445
ContentType Journal Article
Copyright 2023 The Authors. published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.
2023 The Authors. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.
2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright_xml – notice: 2023 The Authors. published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.
– notice: 2023 The Authors. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.
– notice: 2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
DBID 24P
AAYXX
CITATION
NPM
K9.
7X8
DOI 10.1002/cpdd.1301
DatabaseName Wiley Online Library Open Access
CrossRef
PubMed
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitle CrossRef
PubMed
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitleList ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
CrossRef
PubMed

Database_xml – sequence: 1
  dbid: 24P
  name: Wiley Online Library Open Access
  url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html
  sourceTypes: Publisher
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
EISSN 2160-7648
EndPage 873
ExternalDocumentID 37415567
10_1002_cpdd_1301
CPDD1301
Genre article
Journal Article
GeographicLocations United States--US
GeographicLocations_xml – name: United States--US
GroupedDBID -MK
05W
0R~
1OC
24P
33P
3SF
52U
52V
53G
8-1
AAESR
AAEVG
AAHHS
AAHQN
AAIPD
AAMNL
AANHP
AANLZ
AAONW
AAXRX
AAYCA
AAZKR
ABCUV
ABDBF
ABJNI
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACGOF
ACMXC
ACPOU
ACRPL
ACUHS
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFWVQ
AHBTC
AIACR
AITYG
AIURR
AIWBW
AJBDE
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZFZN
AZVAB
BDRZF
BFHJK
BHBCM
BMXJE
BNHUX
BOGZA
BRXPI
C45
DCZOG
DPXWK
DRFUL
DRMAN
DRSTM
EBS
EJD
FUBAC
G-S
GODZA
H13
HGLYW
KBYEO
LATKE
LEEKS
LH4
LITHE
LOXES
LSO
LUTES
LW6
LYRES
MEWTI
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
MY~
O66
O9-
OVD
P2W
PQQKQ
R.K
ROL
SUPJJ
TEORI
TUS
WBKPD
WIH
WIJ
WIK
WOHZO
WOIKV
WPGGZ
WXSBR
WYJ
ZZTAW
AAYXX
AEYWJ
AGHNM
AGQPQ
AGYGG
CITATION
NPM
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
K9.
7X8
ID FETCH-LOGICAL-c3881-401ec7183d2d76f48bb9106635b65e61416bd284be62e52bd9d408d9ffead95b3
IEDL.DBID 24P
ISSN 2160-763X
2160-7648
IngestDate Fri Jul 11 15:25:18 EDT 2025
Fri Jul 25 22:49:54 EDT 2025
Wed Feb 19 02:24:13 EST 2025
Thu Apr 24 23:02:37 EDT 2025
Tue Jul 01 00:19:15 EDT 2025
Wed Jan 22 16:15:13 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 9
Keywords pharmacokinetics
ustekinumab
ABP 654
biosimilar
Language English
License Attribution
2023 The Authors. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3881-401ec7183d2d76f48bb9106635b65e61416bd284be62e52bd9d408d9ffead95b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Undefined-1
ObjectType-Feature-3
content type line 23
OpenAccessLink https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcpdd.1301
PMID 37415567
PQID 2859432200
PQPubID 2034576
PageCount 11
ParticipantIDs proquest_miscellaneous_2835281397
proquest_journals_2859432200
pubmed_primary_37415567
crossref_primary_10_1002_cpdd_1301
crossref_citationtrail_10_1002_cpdd_1301
wiley_primary_10_1002_cpdd_1301_CPDD1301
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate September 2023
PublicationDateYYYYMMDD 2023-09-01
PublicationDate_xml – month: 09
  year: 2023
  text: September 2023
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Oxford
PublicationTitle Clinical pharmacology in drug development
PublicationTitleAlternate Clin Pharmacol Drug Dev
PublicationYear 2023
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2010; 10
2019; 9
2009; 68
2019; 10
2020; 80
2020; 14
2013; 382
1996; 14
2011; 3
2016; 37
2009; 27
2022; 28
2018; 7
2017; 31
2021; 54
2013; 33
2022
2010; 28
2017; 76
2018; 178
2022; 9
2015; 21
2020; 9
2008; 48
2014; 73
2014; 6
2003; 20
2022; 16
2008; 371
2005; 35
2018; 36
e_1_2_10_23_1
e_1_2_10_24_1
e_1_2_10_21_1
e_1_2_10_22_1
e_1_2_10_20_1
Mulcahy AW (e_1_2_10_5_1) 2018; 7
e_1_2_10_2_1
e_1_2_10_4_1
e_1_2_10_18_1
e_1_2_10_3_1
e_1_2_10_19_1
e_1_2_10_6_1
e_1_2_10_16_1
e_1_2_10_8_1
e_1_2_10_14_1
e_1_2_10_7_1
e_1_2_10_15_1
e_1_2_10_12_1
e_1_2_10_9_1
e_1_2_10_13_1
e_1_2_10_10_1
e_1_2_10_33_1
e_1_2_10_32_1
cr-split#-e_1_2_10_11_1.1
e_1_2_10_31_1
cr-split#-e_1_2_10_11_1.2
e_1_2_10_30_1
Iskit AB (e_1_2_10_17_1) 2022; 9
e_1_2_10_29_1
e_1_2_10_27_1
e_1_2_10_28_1
e_1_2_10_25_1
e_1_2_10_26_1
References_xml – volume: 33
  start-page: 291
  issue: 4
  year: 2013
  end-page: 301
  article-title: Comparison of the pharmacokinetics of subcutaneous ustekinumab between Chinese and non‐Chinese healthy male subjects across two Phase 1 studies
  publication-title: Clin Drug Investig
– volume: 28
  start-page: 1527
  issue: 10
  year: 2022
  end-page: 1536
  article-title: The magnitude of Crohn's disease direct costs in health care systems (from different perspectives): a systematic review
  publication-title: Inflamm Bowel Dis
– volume: 7
  start-page: 3
  issue: 4
  year: 2018
  article-title: Biosimilar cost savings in the United States: initial experience and future potential
  publication-title: Rand Health Q
– volume: 6
  start-page: 1178
  issue: 5
  year: 2014
  end-page: 1189
  article-title: Bioanalytical strategy used in development of pharmacokinetic (PK) methods that support biosimilar programs
  publication-title: MAbs
– volume: 14
  start-page: 23
  issue: 1
  year: 2020
  end-page: 32
  article-title: IM‐UNITI: three‐year efficacy, safety, and immunogenicity of ustekinumab treatment of Crohn's disease
  publication-title: J Crohns Colitis
– volume: 9
  start-page: 86
  issue: 1
  year: 2022
  end-page: 91
  article-title: Key concepts in biosimilar medicines: what physicians must know
  publication-title: North Clin Istanb
– volume: 20
  start-page: 1885
  issue: 11
  year: 2003
  end-page: 900
  article-title: Recommendations for the bioanalytical method validation of ligand‐binding assays to support pharmacokinetic assessments of macromolecules
  publication-title: Pharm Res
– volume: 21
  start-page: 719
  issue: 7
  year: 2015
  end-page: 729
  article-title: IL‐12 and IL‐23 cytokines: from discovery to targeted therapies for immune‐mediated inflammatory diseases
  publication-title: Nat Med
– volume: 16
  start-page: 1222
  issue: 6
  year: 2022
  end-page: 1234
  article-title: Efficacy and safety of maintenance ustekinumab for ulcerative colitis through 3 years: UNIFI long‐term extension
  publication-title: J Crohns Colitis
– volume: 36
  start-page: 567
  issue: 5
  year: 2018
  end-page: 589
  article-title: Cost and cost effectiveness of treatments for psoriatic arthritis: a systematic literature review
  publication-title: Pharmacoeconomics
– volume: 9
  start-page: 410
  issue: 9
  year: 2019
  article-title: The breakthrough of biosimilars: a twist in the narrative of biological therapy
  publication-title: Biomolecules
– volume: 178
  start-page: 997
  issue: 5
  year: 2018
  end-page: 998
  article-title: Allocation of biologics: health economics and clinical decision making in plaque psoriasis
  publication-title: Br J Dermatol
– volume: 54
  start-page: 234
  issue: 3
  year: 2021
  end-page: 248
  article-title: Systematic review: societal cost of illness of inflammatory bowel disease is increasing due to biologics and varies between continents
  publication-title: Aliment Pharmacol Ther
– volume: 28
  start-page: 863
  issue: 8
  year: 2010
  end-page: 867
  article-title: Implications of the presence of N‐glycolylneuraminic acid in recombinant therapeutic glycoproteins
  publication-title: Nat Biotechnol
– volume: 371
  start-page: 1675
  issue: 9625
  year: 2008
  end-page: 1684
  article-title: Efficacy and safety of ustekinumab, a human interleukin‐12/23 monoclonal antibody, in patients with psoriasis: 52‐week results from a randomised, double‐blind, placebo‐controlled trial (PHOENIX 2)
  publication-title: Lancet
– volume: 9
  start-page: 2113
  issue: 5
  year: 2020
  end-page: 2119
  article-title: A narrative review of biosimilars: a continued journey from the scientific evidence to practice implementation
  publication-title: Transl Lung Cancer Res
– volume: 76
  start-page: 526
  issue: 3
  year: 2017
  end-page: 533
  article-title: A randomised, single‐blind, single‐dose, three‐arm, parallel‐group study in healthy subjects to demonstrate pharmacokinetic equivalence of ABP 501 and adalimumab
  publication-title: Ann Rheum Dis
– volume: 14
  start-page: 321
  issue: 4
  year: 1996
  end-page: 328
  article-title: Enhancement of antigen presentation of influenza virus hemagglutinin by the natural human anti‐Gal antibody
  publication-title: Vaccine
– volume: 73
  start-page: 990
  issue: 6
  year: 2014
  end-page: 999
  article-title: Efficacy and safety of the anti‐IL‐12/23 p40 monoclonal antibody, ustekinumab, in patients with active psoriatic arthritis despite conventional non‐biological and biological anti‐tumour necrosis factor therapy: 6‐month and 1‐year results of the phase 3, multicentre, double‐blind, placebo‐controlled, randomised PSUMMIT 2 trial
  publication-title: Ann Rheum Dis
– volume: 3
  start-page: 535
  issue: 6
  year: 2011
  end-page: 545
  article-title: Discovery and mechanism of ustekinumab: a human monoclonal antibody targeting interleukin‐12 and interleukin‐23 for treatment of immune‐mediated disorders
  publication-title: MAbs
– volume: 371
  start-page: 1665
  issue: 9625
  year: 2008
  end-page: 1674
  article-title: Efficacy and safety of ustekinumab, a human interleukin‐12/23 monoclonal antibody, in patients with psoriasis: 76‐week results from a randomised, double‐blind, placebo‐controlled trial (PHOENIX 1)
  publication-title: Lancet
– volume: 80
  start-page: 99
  issue: 2
  year: 2020
  end-page: 113
  article-title: The future of biosimilars: maximizing benefits across immune‐mediated inflammatory diseases
  publication-title: Drugs
– year: 2022
– volume: 31
  start-page: 175
  issue: 3
  year: 2017
  end-page: 187
  article-title: Developing the totality of evidence for biosimilars: regulatory considerations and building confidence for the healthcare community
  publication-title: BioDrugs
– volume: 27
  start-page: 3072
  issue: 23
  year: 2009
  end-page: 3082
  article-title: Mechanism for increased immunogenicity of vaccines that form in vivo immune complexes with the natural anti‐Gal antibody
  publication-title: Vaccine
– volume: 37
  start-page: 1946
  issue: 20
  year: 2016
  end-page: 1960
  article-title: Ustekinumab as induction and maintenance therapy for Crohn's disease
  publication-title: N Engl J Med
– volume: 10
  start-page: 279
  year: 2019
  article-title: Biological therapies in immune‐mediated inflammatory diseases: can biosimilars reduce access inequities?
  publication-title: Front Pharmacol
– volume: 48
  start-page: 1267
  issue: 5
  year: 2008
  end-page: 1281
  article-title: Recommendations for the validation of immunoassays used for detection of host antibodies against biotechnology products
  publication-title: J Pharm Biomed Anal
– volume: 382
  start-page: 780
  issue: 9894
  year: 2013
  end-page: 789
  article-title: Efficacy and safety of ustekinumab in patients with active psoriatic arthritis: 1 year results of the phase 3, multicentre, double‐blind, placebo‐controlled PSUMMIT 1 trial
  publication-title: Lancet
– volume: 35
  start-page: 2638
  issue: 9
  year: 2005
  end-page: 2647
  article-title: The influence of natural antibody specificity on antigen immunogenicity
  publication-title: Eur J Immunol
– volume: 68
  start-page: 1739
  issue: 11
  year: 2009
  end-page: 1745
  article-title: Formation of antibodies against infliximab and adalimumab strongly correlates with functional drug levels and clinical responses in rheumatoid arthritis
  publication-title: Ann Rheum Dis
– volume: 10
  start-page: 587
  issue: 4
  year: 2010
  end-page: 604
  article-title: The use of ustekinumab in autoimmune disease
  publication-title: Expert Opin Biol Ther
– ident: e_1_2_10_23_1
  doi: 10.1016/S0140-6736(08)60725-4
– ident: e_1_2_10_4_1
  doi: 10.1517/14712591003724670
– ident: e_1_2_10_3_1
  doi: 10.1038/nm.3895
– ident: #cr-split#-e_1_2_10_11_1.1
  doi: 10.1007/s40268-023-00441-7
– ident: e_1_2_10_14_1
  doi: 10.1136/annrheumdis-2015-208914
– ident: e_1_2_10_29_1
  doi: 10.1093/ecco-jcc/jjac030
– ident: e_1_2_10_19_1
  doi: 10.1038/nbt.1651
– ident: e_1_2_10_10_1
  doi: 10.1007/s40259-017-0218-5
– ident: e_1_2_10_8_1
  doi: 10.3390/biom9090410
– ident: e_1_2_10_16_1
  doi: 10.1007/s40261-013-0072-2
– volume: 7
  start-page: 3
  issue: 4
  year: 2018
  ident: e_1_2_10_5_1
  article-title: Biosimilar cost savings in the United States: initial experience and future potential
  publication-title: Rand Health Q
– ident: e_1_2_10_22_1
  doi: 10.1016/0264-410X(95)00189-8
– ident: #cr-split#-e_1_2_10_11_1.2
– ident: e_1_2_10_2_1
  doi: 10.4161/mabs.3.6.17815
– ident: e_1_2_10_28_1
  doi: 10.1093/ecco-jcc/jjz110
– volume: 9
  start-page: 86
  issue: 1
  year: 2022
  ident: e_1_2_10_17_1
  article-title: Key concepts in biosimilar medicines: what physicians must know
  publication-title: North Clin Istanb
– ident: e_1_2_10_25_1
  doi: 10.1016/S0140-6736(13)60594-2
– ident: e_1_2_10_24_1
  doi: 10.1016/S0140-6736(08)60726-6
– ident: e_1_2_10_15_1
  doi: 10.1016/j.jpba.2008.09.020
– ident: e_1_2_10_9_1
  doi: 10.21037/tlcr-20-601
– ident: e_1_2_10_13_1
  doi: 10.4161/mabs.32114
– ident: e_1_2_10_21_1
  doi: 10.1002/eji.200526146
– ident: e_1_2_10_27_1
  doi: 10.1056/NEJMoa1602773
– ident: e_1_2_10_30_1
  doi: 10.1111/bjd.16504
– ident: e_1_2_10_18_1
  doi: 10.1136/ard.2008.092833
– ident: e_1_2_10_7_1
  doi: 10.1007/s40265-020-01256-5
– ident: e_1_2_10_31_1
  doi: 10.1007/s40273-018-0618-5
– ident: e_1_2_10_33_1
  doi: 10.1093/ibd/izab334
– ident: e_1_2_10_6_1
  doi: 10.3389/fphar.2019.00279
– ident: e_1_2_10_12_1
  doi: 10.1023/B:PHAM.0000003390.51761.3d
– ident: e_1_2_10_20_1
  doi: 10.1016/j.vaccine.2009.03.019
– ident: e_1_2_10_26_1
  doi: 10.1136/annrheumdis-2013-204655
– ident: e_1_2_10_32_1
  doi: 10.1111/apt.16445
SSID ssj0000601114
Score 2.349766
Snippet ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin‐12 and interleukin‐23. Ustekinumab RP is...
ABP 654 is a proposed biosimilar to ustekinumab reference product (RP) which works through antagonism of interleukin-12 and interleukin-23. Ustekinumab RP is...
SourceID proquest
pubmed
crossref
wiley
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 863
SubjectTerms ABP 654
Biological products
biosimilar
Cytokines
Double-blind studies
Monoclonal antibodies
Pharmacokinetics
ustekinumab
Title Pharmacokinetic Similarity of ABP 654, an Ustekinumab Biosimilar Candidate: Results from a Randomized, Double‐blind Study in Healthy Subjects
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcpdd.1301
https://www.ncbi.nlm.nih.gov/pubmed/37415567
https://www.proquest.com/docview/2859432200
https://www.proquest.com/docview/2835281397
Volume 12
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3NatwwEBYhufRS-t9t0zAtJeSwJrYsy3Z72p8uodBi0izszUiWDCa7dqh3D5tT3qB9xj5JZ-y1l9AWerPRGGPPjObTSPMNY--5yGM0BOVI6_qOyFToaN-GTsxtpGNEyK6gAucvX-XFXHxeBIsD9rGrhWn5IfqEG3lGM1-Tgytdn-9JQ7MbY6iXMS59jqi0ls7zcZH0CRYiGvEabm_uSddBP1p0zEIuP--fvh-P_gCZ9zFrE3Rmj9jDHVqEUavex-zAlk_YadLSTW-HcLWvnqqHcArJnoh6-5T96G6v8WNRBL4VqwJXsgi8ocphNE5ABmIIqoQ5KhulNiulYVxUdSsIEyp6oZzAB7i09Wa5roHqUUDBJY5Uq-LWmiEgCNdL--vup8a_aoCOJm6hKKEtcdoCTk6U7amfsfns09Xkwtk1YHAyP4pobenZDIOXb7gJZS4irRFdEEbRMrAY2D2pDcY3bSW3AdcmNsKNTJznaJ9xoP3n7LCsSvuSgY58HYVaBbm1IhS5ipXwfasiGaowC8yAnXVqSLMdOzk1yVimLa8yT0ljtPnmDdi7XvSmpeT4m9Bxp8t055V1SmR9Amcw1x2wt_0w-hNtkqjSVhuSIb4bwsUD9qK1gf4tfgO_JI6cNUbx79enk2Q6pYtX_y_6mj2gXvbtAbZjdrj-vrFvEPGs9Ulj2SfsaDSejme_AUea_sw
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NbtNAEF6VcoAL4p-0BQYEVQ-xaq_XaxuJQ5tQpfRHUUmk3Myudy1FJHaFE6Fw4g3gQXgqnoQZO3FUARKX3mztyLY8f9_O7nzL2CsushgNQTnSur4jUhU62rehE3Mb6RgRsiuowfnsXPaG4v0oGG2wn6temJofoim4kWdU8ZocnArS-2vW0PTSGDrM2FtuqTyxiy84YSvfHndRu685P3o36PSc5ZkCTupHEU2XPJtiPPYNN6HMRKQ1JkxKu1oGFnOVJ7XBkK2t5Dbg2sRGuJGJswx_eRxoH597g90Ukod0XgIX_aaiQ8wmXkUmzj3pOui4oxWVkcv3m6-9mgD_QLVXQXKV5Y7usjtLeAoHtT3dYxs2v892-zW_9aINg3W7VtmGXeivma8XD9j31e0n_LsoAh_G0zFOnRHpQ5HBwWEfZCDaoHIYonWh1HyqNByOi7IWhA512VAR4g1c2HI-mZVADTCg4AJHiun4qzVtQNSvJ_bXtx8a1WiA9kIuYJxD3VO1AIyGVF4qH7LhtWjnEdvMi9w-YaAjX0ehVkFmrQhFpmIlfN-qSIYqTAPTYnsrNSTpkg6dTuWYJDWRM09IY7Ta57XYy0b0suYA-ZvQzkqXyTIMlAmxAwoMma7bYi-aYXRgWpVRuS3mJEMEOwTEW-xxbQPNW_wK70kc2auM4t-vTzr9bpcutv5f9Dm71RucnSanx-cn2-w2R_hW757bYZuzz3P7FOHWTD-rrBzYx-t2q98rvDpL
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3LbtNAFB2VIiE2iDeBAhcEVRexao_HLyQWbULUUqis0kjZmRnPWIpI7AgnQmHFH8B_8Fd8Cff6FVWAxKY7W3Plsea-zjzuGcZecJFFaAjS8o3tWiKVgaVcE1gRN6GKECHbggqc35_6R2PxduJNttjPtham5ofoFtzIM6p4TQ6-0Nn-hjQ0XWhNdxk7zYnKE7P-gvO18vXxEJX7kvPRm_PBkdVcKWClbhjSbMkxKYZjV3Md-JkIlcJ8SVlX-Z7BVOX4SmPEVsbnxuNKR1rYoY6yDEc88pSL373CrtLmIp0f4yLuFnSI2MSpuMS549sW-u2kZTKy-X73txfz3x-g9iJGrpLc6Ca70aBTOKjN6RbbMvltthvX9NbrPpxvqrXKPuxCvCG-Xt9h39vXTzi4KAIfpvMpzpwR6EORwcFhDL4n-iBzGKNxodRqLhUcTouyFoQBFdnQGsQrODPlarYsgepfQMIZthTz6Vej-4CgX83Mr28_FGpRAx2FXMM0h7qkag0YDGl1qbzLxpeinXtsOy9y84CBCl0VBkp6mTEiEJmMpHBdI0M_kEHq6R7ba9WQpA0bOl3KMUtqHmeekMZos8_pseed6KKmAPmb0E6ry6SJAmVC5IACI6Zt99izrhn9lzZlZG6KFckQvw7h8B67X9tA14tbwT0fW_Yqo_h398kgHg7p4eH_iz5l1-LhKHl3fHryiF3nCN7qs3M7bHv5eWUeI9haqieVkQP7eNle9RsJ8zl9
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Pharmacokinetic+Similarity+of+ABP+654%2C+an+Ustekinumab+Biosimilar+Candidate%3A+Results+from+a+Randomized%2C+Double-blind+Study+in+Healthy+Subjects&rft.jtitle=Clinical+pharmacology+in+drug+development&rft.au=Chow%2C+Vincent&rft.au=Mytych%2C+Daniel+T&rft.au=Das%2C+Shyamal&rft.au=Franklin%2C+Janet&rft.date=2023-09-01&rft.eissn=2160-7648&rft_id=info:doi/10.1002%2Fcpdd.1301&rft_id=info%3Apmid%2F37415567&rft.externalDocID=37415567
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2160-763X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2160-763X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2160-763X&client=summon