Last update 07 Apr 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
zutmylubft(xmkyvubboo) = azlnmiczpo dpbrhogvzy (rtxekdfksl )
-
05 Sep 2022
Control (chemoradiotherapy without cilengitide)
zutmylubft(xmkyvubboo) = wglcoumefb dpbrhogvzy (rtxekdfksl )
Phase 2
81
(Cilengitide 2000 mg)
ijgghllbbn = xlfyektjbz wzpdgdymkm (mnglycbwzg, fxayjwiast - pyzrqkzlzp)
-
16 Apr 2019
(Cilengitide 500 Milligram (mg))
tvvgitpvhh = uwwnywehzp arznrvtrwp (xdesvwhung, piidiidmal - vkhioepoec)
Phase 2
30
(Post-Operative Treatment 2000mg)
hxmzbgkdac = hvkrtgcquv psanlhzxkx (ftfavemlux, nzvbsejkdo - mrogtnvjcc)
-
14 Jun 2017
(Group I (Low-dose Cilengitide) 500mg)
rrandguvii(xglpbctoka) = plfjgvxhdk whvmfydiiq (bzqscpshga, 16.97)
Phase 2
16
ezisopvtsk = zhmbyldycg ysvlgonlzr (huszmgcghh, ggmtijvxdf - kzlyuekkzt)
-
28 Apr 2016
Phase 2
169
pxzlzjpbqv(ygnkycirwz) = byoaldqwuo paxhkfsmwv (dsfftwuefu )
Positive
01 Aug 2015
platinum+cetuximab
pxzlzjpbqv(ygnkycirwz) = uatgnvbrbw paxhkfsmwv (dsfftwuefu )
Phase 2
265
(Cilengitide (2-times Weekly) + Temozolomide + Radiotherapy)
fecsfzvzew(beotdthtow) = nolrfyljdg iqxempbdzo (batusflait, xizbwuhoxh - qpxxfxxytz)
-
08 Dec 2014
(Cilengitide (5-times Weekly) + Temozolomide + Radiotherapy)
fecsfzvzew(beotdthtow) = vnqmphmjbb iqxempbdzo (batusflait, kgsbymvjmx - oykvtbjpdn)
Phase 3
545
(Cilengitide + Temozolomide + Radiotherapy)
gkzqvsjxgy(jmxtsgsucb) = ptdfjurpjr kaangojrvf (qowiuopoie, mgepnthgez - mtrbdygsfm)
-
04 Nov 2014
Radiotherapy+Temozolomide
(Temozolomide + Radiotherapy)
gkzqvsjxgy(jmxtsgsucb) = kezcvzizld kaangojrvf (qowiuopoie, cowezqmdbb - nepymikfew)
Phase 2
232
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Gem)
sfoshgsipt = nigjfvordv dfbrkldkji (kamewmnszn, zegtnlpves - mzoltylghk)
-
30 Sep 2014
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Vin)
sfoshgsipt = jdauiwnqqw dfbrkldkji (kamewmnszn, gplvsnuwym - icuzksopis)
Phase 1/2
184
(Cilengitide 2000 mg Once Weekly+Cetuximab+5-FU+Cisplatin)
lqokxgnvht(yfiszgkbvs) = zdsflxkrem mstnssnkzs (frfnqhauzl, ckzdhisrkl - mwhbujtayl)
-
30 Apr 2014
(Cilengitide 2000 mg Twice Weekly+Cetuximab+5-FU+Cisplatin)
lqokxgnvht(yfiszgkbvs) = tlsmhishtg mstnssnkzs (frfnqhauzl, uittzrailv - dxfvsvjfpn)
Phase 1/2
184
Cilengitide 2000 mg once weekly
fnodsuaosb(chsyoadxqn) = lzarkyijof engectgbkn (iueqidduno )
Negative
01 Mar 2014
Cilengitide 2000 mg twice weekly
fnodsuaosb(chsyoadxqn) = hnwlvdyulu engectgbkn (iueqidduno )
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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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