Last update 23 Jan 2025

MT-0814

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Target
CCR3
Mechanism
CCR3 antagonists(C-C chemokine receptor type 3 antagonists)
Therapeutic Areas
Congenital DisordersEye Diseases
Active Indication
Dystrophy, Macular
Inactive Indication
Age Related Macular DegenerationWet Macular Degeneration
Originator Organization
Mitsubishi Tanabe Pharma Corp.Mitsubishi Tanabe Pharma Corp.
Active Organization
Mitsubishi Tanabe Pharma Corp.Mitsubishi Tanabe Pharma Corp.
Inactive Organization
Senju Pharmaceutical Co., Ltd.
Drug Highest PhasePhase 2
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with MT-0814
NCT03869684
/ TerminatedPhase 2
A Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study to Assess the Safety, Tolerability, and Efficacy of MT-0814 for the Treatment of Patients With Age-Related Macular Degeneration
100 Clinical Results associated with MT-0814
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100 Translational Medicine associated with MT-0814
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100 Patents (Medical) associated with MT-0814
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100 Deals associated with MT-0814
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Wet Macular DegenerationPhase 2
US
Mitsubishi Tanabe Pharma Corp.Mitsubishi Tanabe Pharma Corp.
18 Mar 2019
Dystrophy, MacularPhase 2-
Mitsubishi Tanabe Pharma Corp.Mitsubishi Tanabe Pharma Corp.
-
Age Related Macular DegenerationDiscovery
US
Senju Pharmaceutical Co., Ltd.
25 Feb 2019
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT03869684 (CTgov)
Phase 2
Age Related Macular Degeneration
13
Placebo
(Placebo)
ytkgcbkacb(cgkpngghpb) = axxrcsloso hnoqtftlsh (vfmhnhaqdb, kbmnnvxtmq - ztkeloflug)
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-
20 Apr 2021
Placebo+MT-0814
(MT-0814 Low Dose)
ytkgcbkacb(cgkpngghpb) = yidpbigqdl hnoqtftlsh (vfmhnhaqdb, jsomutqjfx - bwktvkhmxs)
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Translational Medicine

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Clinical Trial

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Approval

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Regulation

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