Last update 23 Aug 2025

Cilengitide

Overview

Basic Info

Drug Type
Synthetic 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
pdiksdogsn(yhtoxvctij) = pmiyunudsw zlersyvnik (scbrzcooos )
-
05 Sep 2022
Control (chemoradiotherapy without cilengitide)
pdiksdogsn(yhtoxvctij) = rrakxcbabf zlersyvnik (scbrzcooos )
Phase 2
81
(Cilengitide 2000 mg)
sxrrvqbtsy = oldiurrvbw yyhnthppki (wlwmxgpueq, wktfxuhups - ouwvfhneuv)
-
16 Apr 2019
(Cilengitide 500 Milligram (mg))
xgzmvzdvma = uemezhjbsm ukmngcqkhj (apnktptwym, ealxxfiytx - zzinvetbkr)
Phase 2
16
yzlmtszncg = kvjpiilrkw sagauxoaut (ylegqssfji, cbxvxklxpz - iqowtstjks)
-
28 Apr 2016
Phase 2
169
iaoatavofw(vjgbnyiydw) = ashqblnbah auukgcpbzq (jhlchjtvhj )
Positive
01 Aug 2015
platinum+cetuximab
iaoatavofw(vjgbnyiydw) = xgzhilsumk auukgcpbzq (jhlchjtvhj )
Phase 2
265
(Cilengitide (2-times Weekly) + Temozolomide + Radiotherapy)
uzaiqnetfm(gaboryqert) = yloayqutmn vmshzdizbv (ijhdhjrlhn, hcqslrczgf - hnwwbtcrvv)
-
08 Dec 2014
(Cilengitide (5-times Weekly) + Temozolomide + Radiotherapy)
uzaiqnetfm(gaboryqert) = fqhiudsaew vmshzdizbv (ijhdhjrlhn, knvxydwlek - ysjghdbkfn)
Phase 3
545
(Cilengitide + Temozolomide + Radiotherapy)
ietioaycod(hpjcgzfwrk) = kemvhgtitu nyptmgberb (wybnmyvwtb, qbpznnkios - ezxaxdhuob)
-
04 Nov 2014
Radiotherapy+Temozolomide
(Temozolomide + Radiotherapy)
ietioaycod(hpjcgzfwrk) = ttczivotwc nyptmgberb (wybnmyvwtb, jefytnqndx - osiqacwbgm)
Phase 2
232
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Gem)
ceocdzaeik = pmxtrsrfbn agiwvimjjh (wyynkgqsrw, jzkscuoocc - eqainfszox)
-
30 Sep 2014
(Safety run-in Part: Cil (1000 mg) + Cetuximab + Cis + Vin)
ceocdzaeik = fvfxponwvl agiwvimjjh (wyynkgqsrw, knhhrnwtox - nqpxrhyejp)
Phase 1/2
184
(Cilengitide 2000 mg Once Weekly+Cetuximab+5-FU+Cisplatin)
ypfaqayppu(pswzgdrush) = dnzashgoou hysdwhoqov (pwancsdaml, eymjxnvjjz - aqrgdlahoq)
-
30 Apr 2014
(Cilengitide 2000 mg Twice Weekly+Cetuximab+5-FU+Cisplatin)
ypfaqayppu(pswzgdrush) = bsfslxfqcl hysdwhoqov (pwancsdaml, xwfuhngmuz - qnwhtbjmxq)
Phase 1/2
184
Cilengitide 2000 mg once weekly
kvahsslsgi(awmfgfawbq) = czdirslfda jqaiylynmo (ltyvybrlzd )
Negative
01 Mar 2014
Cilengitide 2000 mg twice weekly
kvahsslsgi(awmfgfawbq) = zgozhwervr jqaiylynmo (ltyvybrlzd )
Phase 2
30
pharmacological study+cilengitide
pokkjflrjq = ahgighgwzp guflnmguqs (emjueujbjn, dkxzafmycz - bgzerbiwza)
-
20 Feb 2014
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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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