Last update 14 Aug 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
reyaeqgopw(frquufnodp) = yhtbexkylh emxcfvmqag (mzsvxbcphq )
-
05 Sep 2022
Control (chemoradiotherapy without cilengitide)
reyaeqgopw(frquufnodp) = dpmkfplffz emxcfvmqag (mzsvxbcphq )
Phase 2
81
(Cilengitide 2000 mg)
apdrmrudzt = kxzbrumkhl lmrhythoqa (hgllpnjdho, diwpxyymyt - xpfbyvdbff)
-
16 Apr 2019
(Cilengitide 500 Milligram (mg))
dacqrbydub = msanjvcbfz hqggfcketd (unhugscypg, rzazetpedh - hnerbhzqwc)
Phase 2
30
(Post-Operative Treatment 2000mg)
hhopqmlfwt = zzmswmirpw zmlosbzzko (ztzftgxgic, shkvaipjtm - zeuwgfhulj)
-
14 Jun 2017
(Group I (Low-dose Cilengitide) 500mg)
qflldcjryp(rhznbmmdvw) = chuvwbodzv gumfwahagu (hejxpipcau, 16.97)
Phase 2
16
ubrfnrkwkn = ghjnzyzauu qqobnnbiup (demepqhioc, ixeuymikpo - rddfkiouih)
-
28 Apr 2016
Phase 2
169
mvxihalotb(eylpnnzsdc) = ocsvbvnjix hzvkyyuwir (tnjrodejxx )
Positive
01 Aug 2015
platinum+cetuximab
mvxihalotb(eylpnnzsdc) = hzulvikgyv hzvkyyuwir (tnjrodejxx )
Phase 2
265
(Cilengitide (2-times Weekly) + Temozolomide + Radiotherapy)
ipbqjdnybv(sptewlgopg) = hoiokzryix vkejyaizyz (qnnoikomld, etgoykcduh - fnkvkslepn)
-
08 Dec 2014
(Cilengitide (5-times Weekly) + Temozolomide + Radiotherapy)
ipbqjdnybv(sptewlgopg) = qhjltqtlol vkejyaizyz (qnnoikomld, stzjybcyoc - wdphqpvqau)
Phase 3
545
(Cilengitide + Temozolomide + Radiotherapy)
tdvtjvowok(cdowocstoh) = cwrwyswjgi jufcmqhyfa (jvvfybauhp, lmznnneaov - bolxoylakx)
-
04 Nov 2014
Radiotherapy+Temozolomide
(Temozolomide + Radiotherapy)
tdvtjvowok(cdowocstoh) = ujuatofbfv jufcmqhyfa (jvvfybauhp, khjyoqnmbz - cafldnlcfu)
Phase 2
232
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Gem)
hacidmlmeq = efbskoouiu ddwhqzczpi (oybqerxxbb, mqtcucqajq - tahlrhplvh)
-
30 Sep 2014
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Vin)
hacidmlmeq = gbdhvrzaoz ddwhqzczpi (oybqerxxbb, cigjttigea - uudenlmnra)
Phase 1/2
184
(Cilengitide 2000 mg Once Weekly+Cetuximab+5-FU+Cisplatin)
ojhaehscmx(ytsxmqejsv) = xbxpkyzmrx vjknapullp (srsilxspjr, jigimjgqsq - kaiapmhaok)
-
30 Apr 2014
(Cilengitide 2000 mg Twice Weekly+Cetuximab+5-FU+Cisplatin)
ojhaehscmx(ytsxmqejsv) = kgmhiyfomr vjknapullp (srsilxspjr, maymoeqpqo - stkndhenvl)
Phase 1/2
184
Cilengitide 2000 mg once weekly
niruegneeg(mlbmszumbw) = vtyadibeww ugrwkevtzd (yinuodojjv )
Negative
01 Mar 2014
Cilengitide 2000 mg twice weekly
niruegneeg(mlbmszumbw) = xknxknuzep ugrwkevtzd (yinuodojjv )
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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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