Last update 20 May 2025

Nimotuzumab biosimilar(El Kendi Pharmaceuticals Manufacturing Company)

Overview

Basic Info

Drug Type
Biosimilar, Monoclonal antibody
Synonyms-
Target
EGFR
Action
antagonists
Mechanism
EGFR antagonists(Epidermal growth factor receptor erbB1 antagonists)
Therapeutic Areas
NeoplasmsUrogenital Diseases
Active Indication-
Inactive Indication
Uterine Cervical Cancer
Originator Organization
El Kendi Pharmaceutical Manufacturing Co.
Active Organization-
Inactive Organization
El Kendi Pharmaceutical Manufacturing Co.
License Organization-
Drug Highest PhasePendingPhase 3
First Approval Date-
Regulation-
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Structure/Sequence

Related

1
Clinical Trials associated with Nimotuzumab biosimilar(El Kendi Pharmaceuticals Manufacturing Company)
EUCTR2007-000338-38-DE
/ Not yet recruitingNot Applicable
A RANDOMIZED, MULTICENTER, PHASE IIB/IIIA STUDY OF GEMCITABINE AND THE MONOCLONAL ANTIBODY NIMOTUZUMAB (OSAG 101) VERSUS GEMCITABINE AND PLACEBO FOR THE TREAMENT OF CHEMOTHERAPY-NAIVE PATIENTS WITH LOCALLY ADVANCED OR METASTATIC PANCREATIC CANCER
100 Clinical Results associated with Nimotuzumab biosimilar(El Kendi Pharmaceuticals Manufacturing Company)
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100 Translational Medicine associated with Nimotuzumab biosimilar(El Kendi Pharmaceuticals Manufacturing Company)
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100 Patents (Medical) associated with Nimotuzumab biosimilar(El Kendi Pharmaceuticals Manufacturing Company)
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100 Deals associated with Nimotuzumab biosimilar(El Kendi Pharmaceuticals Manufacturing Company)
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External Link

KEGGWikiATCDrug Bank
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DB06192

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Uterine Cervical CancerPhase 3
Algeria
El Kendi Pharmaceutical Manufacturing Co.
01 Nov 2015
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Translational Medicine

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Deal

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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.
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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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