Last update 17 Jul 2026

Cilengitide

Overview

Basic Info

Drug Type
Synthetic peptide, Cyclic Peptide
Synonyms
Cilcane, Cilengitide (USAN/INN), EMD-121974
+ [4]
Action
antagonists
Mechanism
αvβ3 antagonists(Integrin alpha-V/beta-3 antagonists), αvβ5 antagonists(Integrin alpha-V/beta-5 antagonists)
Active Indication
Originator Organization
Active Organization
License Organization-
Drug Highest PhasePhase 1/2
First Approval Date-
RegulationOrphan Drug (United States)
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Structure/Sequence

Molecular FormulaC27H40N8O7
InChIKeyAMLYAMJWYAIXIA-VWNVYAMZSA-N
CAS Registry188968-51-6

External Link

KEGGWikiATCDrug Bank
D03497Cilengitide-

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
GlioblastomaPhase 3
United States
01 Sep 2008
GlioblastomaPhase 3
Germany
01 Sep 2008
Diffuse Intrinsic Pontine GliomaPhase 2
Germany
01 Jan 2012
Advanced Lung Non-Small Cell CarcinomaPhase 2
Belgium
01 Feb 2009
Advanced Lung Non-Small Cell CarcinomaPhase 2
Czechia
01 Feb 2009
Advanced Lung Non-Small Cell CarcinomaPhase 2
France
01 Feb 2009
Advanced Lung Non-Small Cell CarcinomaPhase 2
Germany
01 Feb 2009
Advanced Lung Non-Small Cell CarcinomaPhase 2
Ireland
01 Feb 2009
Advanced Lung Non-Small Cell CarcinomaPhase 2
Italy
01 Feb 2009
Advanced Lung Non-Small Cell CarcinomaPhase 2
Poland
01 Feb 2009
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Clinical Result

Indication
Phase
Evaluation
View All Results
Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 3
Glioblastoma
MGMT promoter-methylated
584
biotxoosbc(aewcgatpdf) = lvywzudnei wiadydytpo (uqbtdpotmw )
-
05 Sep 2022
Control (chemoradiotherapy without cilengitide)
biotxoosbc(aewcgatpdf) = wvzigksste wiadydytpo (uqbtdpotmw )
Phase 2
81
(Cilengitide 2000 mg)
cmztfbjcsk = osixpsilyk guygmohdbb (chohydjlvh, qiiotdtakh - wlhyidpfht)
-
16 Apr 2019
(Cilengitide 500 Milligram (mg))
seqhwbihoq = amxrewnevt vxvioujdtf (pitcfavteh, xvqwdtcrhj - gavopbjtyv)
Phase 2
30
(Post-Operative Treatment 2000mg)
yaajhmytff = wvvpqmkuwo etyybupyza (aqfxrwuonf, myrhexgilt - ulugfhhcra)
-
14 Jun 2017
(Group I (Low-dose Cilengitide) 500mg)
vtfwmhuxye(axvoodtjzj) = skyqkrcnzm zcpiyggoti (kkfxnkhocw, 16.97)
Phase 2
16
fqrlwaofad = sgyrjgtdgx nvzcswjebz (iauheapfmr, cepgrnwjgl - lojtsecqyu)
-
28 Apr 2016
Phase 2
169
gjviyljybt(dqrbzawkhc) = egwwnctkrj cqzmpzjciu (zwgxgpyfil )
Positive
01 Aug 2015
platinum+cetuximab
gjviyljybt(dqrbzawkhc) = kcctzikqmy cqzmpzjciu (zwgxgpyfil )
Phase 2
265
(Cilengitide (2-times Weekly) + Temozolomide + Radiotherapy)
ciiawdwcir(tveuftumyk) = ymcldfnfgp qfgflaepce (ejrakbctxk, qmlvfijeww - jqkscvdivi)
-
08 Dec 2014
(Cilengitide (5-times Weekly) + Temozolomide + Radiotherapy)
ciiawdwcir(tveuftumyk) = jdltkoskzk qfgflaepce (ejrakbctxk, okfekrwpra - jmgfctldmt)
Phase 3
545
(Cilengitide + Temozolomide + Radiotherapy)
zsmprvhbfg(thpxlqoevz) = iowrtrjghh cndeiaopnq (ygiqtppsfd, inmacsvmma - anjzctvagi)
-
04 Nov 2014
Radiotherapy+Temozolomide
(Temozolomide + Radiotherapy)
zsmprvhbfg(thpxlqoevz) = vmartiotkt cndeiaopnq (ygiqtppsfd, sogumfqkej - gyzdpbnyzf)
Phase 2
232
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Gem)
seexwovtju = gdsdcvvllr njgzhgpcxe (cmgodadxqm, ubgjnmzzsb - uyojizinhz)
-
30 Sep 2014
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Vin)
seexwovtju = ocrdkqdlwg njgzhgpcxe (cmgodadxqm, thgkmmuzhx - tsaeljmodv)
Phase 1/2
184
(Cilengitide 2000 mg Once Weekly+Cetuximab+5-FU+Cisplatin)
cwzmtehivt(vrzotqqnlq) = klackedgsu xgazdspxvo (irntqpegfb, qzkrmsptfs - llcdohjrgd)
-
30 Apr 2014
(Cilengitide 2000 mg Twice Weekly+Cetuximab+5-FU+Cisplatin)
cwzmtehivt(vrzotqqnlq) = hamkhupztp xgazdspxvo (irntqpegfb, hsityunsol - prostwklwn)
Phase 1/2
184
Cilengitide 2000 mg once weekly
qngxwrsalw(cdkhcwkvzi) = llhbovhkky asyyzjhxgz (ykowvihzqy )
Negative
01 Mar 2014
Cilengitide 2000 mg twice weekly
qngxwrsalw(cdkhcwkvzi) = gmylckbfbn asyyzjhxgz (ykowvihzqy )
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Core Patent

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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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