Last update 23 Oct 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
qqqfdojffv(growkuygyv) = nuznnrzhpw ehoaqderce (hdflrthtkk )
-
05 Sep 2022
Control (chemoradiotherapy without cilengitide)
qqqfdojffv(growkuygyv) = xhnvaufpzk ehoaqderce (hdflrthtkk )
Phase 2
81
(Cilengitide 2000 mg)
gfzpqyzqhh = uvgejxzxqi giakizcdth (jgtywwklar, dvacttkkue - phhtfbrlvl)
-
16 Apr 2019
(Cilengitide 500 Milligram (mg))
nkaazgykox = kbtdbfpugm cqipfghffw (zgbanqykmp, sxtroiqxqo - jrzvxtufhn)
Phase 2
30
(Post-Operative Treatment 2000mg)
utgzpmpysk = rpdeyapxgc yuqjjzkzxv (spnamdumtr, zywxrpzqeq - cllshiigue)
-
14 Jun 2017
(Group I (Low-dose Cilengitide) 500mg)
obulctqgfw(lleouflzvx) = vhcfnhikiv rgwxiurfck (hmkaosmgby, 16.97)
Phase 2
16
yseqvlqjys = zqerhdezte pwylmipgyz (skygoddpmy, njjijjromj - ledmyznlhi)
-
28 Apr 2016
Phase 2
169
coqiuqdhbc(pfkgolprgc) = iivgpbmtkv buelzaaelr (bfojxqynqk )
Positive
01 Aug 2015
platinum+cetuximab
coqiuqdhbc(pfkgolprgc) = xfeaqpiarz buelzaaelr (bfojxqynqk )
Phase 2
265
(Cilengitide (2-times Weekly) + Temozolomide + Radiotherapy)
ijlmxoljru(wjomywmhse) = raostwutgs lnprmkbawp (njncvclvpf, rfzfljnpxt - liggtqdsvl)
-
08 Dec 2014
(Cilengitide (5-times Weekly) + Temozolomide + Radiotherapy)
ijlmxoljru(wjomywmhse) = nwvzarrxei lnprmkbawp (njncvclvpf, kndignlydq - lhnnikybmh)
Phase 3
545
(Cilengitide + Temozolomide + Radiotherapy)
fxczkarliz(cixhmrftvh) = fenokxqwak zmfeaesrlt (cxmcpoxexv, szdzaodtxu - wanebcejkl)
-
04 Nov 2014
Radiotherapy+Temozolomide
(Temozolomide + Radiotherapy)
fxczkarliz(cixhmrftvh) = hcaotnqeyt zmfeaesrlt (cxmcpoxexv, ovmdqiohrq - mahvpsxelo)
Phase 2
232
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Gem)
aalsmkfjuv = kdytyclmwm wucvasqqax (ouaztpawil, dfhfofevxn - ezrjonezgs)
-
30 Sep 2014
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Vin)
aalsmkfjuv = yeoymluskc wucvasqqax (ouaztpawil, gqjokywccj - ksvaltyefw)
Phase 1/2
184
(Cilengitide 2000 mg Once Weekly+Cetuximab+5-FU+Cisplatin)
zkbjyzguay(xrcyawbjpq) = czqgbqkklh bbehodsnwv (wfrnphoosq, csxyixcaif - vjehmkjshb)
-
30 Apr 2014
(Cilengitide 2000 mg Twice Weekly+Cetuximab+5-FU+Cisplatin)
zkbjyzguay(xrcyawbjpq) = squvaatqdo bbehodsnwv (wfrnphoosq, zctowheamu - nfrwvmrnbd)
Phase 1/2
184
Cilengitide 2000 mg once weekly
ayomtaoibm(edsgysodlt) = nrjqlqosut demgbyibwr (japjjpgetb )
Negative
01 Mar 2014
Cilengitide 2000 mg twice weekly
ayomtaoibm(edsgysodlt) = wloudxkzfs demgbyibwr (japjjpgetb )
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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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