Last update 11 Sep 2026

Yttrium Y 90 monoclonal antibody MN-14(NCI)

Overview

Basic Info

Drug Type
Radiolabeled antibody, Therapeutic radiopharmaceuticals
Synonyms-
Target
CEACAM5
Action
modulators
Mechanism
CEACAM5 modulators(Carcinoembryonic antigen related cell adhesion molecule 5 modulators)
Therapeutic Areas
NeoplasmsDigestive System DisordersEndocrinology and Metabolic Disease+ [3]
Active Indication-
Inactive Indication
Colorectal CancerMetastatic breast cancerOvarian Epithelial Carcinoma+ [2]
Originator Organization
National Cancer InstituteNational Cancer Institute
Active Organization-
Inactive Organization
National Cancer InstituteNational Cancer InstituteGarden State Cancer Center
License Organization-
Drug Highest PhasePendingPhase 1/2
First Approval Date-
Regulation-
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Structure/Sequence

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Related

100 Clinical Results associated with Yttrium Y 90 monoclonal antibody MN-14(NCI)
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100 Translational Medicine associated with Yttrium Y 90 monoclonal antibody MN-14(NCI)
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100 Patents (Medical) associated with Yttrium Y 90 monoclonal antibody MN-14(NCI)
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100 Deals associated with Yttrium Y 90 monoclonal antibody MN-14(NCI)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Ovarian Epithelial CarcinomaPhase 2
United States
National Cancer InstituteNational Cancer Institute
31 Aug 1999
Thyroid Cancer, MedullaryPhase 2
United States
Garden State Cancer Center
30 Sep 1998
Metastatic breast cancerPhase 2
United States
National Cancer InstituteNational Cancer Institute
31 May 1998
Colorectal CancerPhase 2
United States
National Cancer InstituteNational Cancer Institute
31 Mar 1997
Pancreatic CancerPhase 2
United States
National Cancer InstituteNational Cancer Institute
31 Mar 1997
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

No Data

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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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