Last update 08 May 2025

Freeze-Dried Live Attenuated Measles And Rubella Combined Vaccine(Takeda)

Overview

Basic Info

Drug Type
Combination vaccine, Live attenuated vaccine, Prophylactic vaccine
Synonyms-
Target-
Action
stimulants
Mechanism
Immunostimulants
Therapeutic Areas
Infectious DiseasesOther Diseases
Active Indication
MeaslesRubella
Inactive Indication-
Originator Organization
Takeda Pharmaceutical Co., Ltd.Takeda Pharmaceutical Co., Ltd.
Active Organization
Takeda Pharmaceutical Co., Ltd.Takeda Pharmaceutical Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhaseApproved
First Approval Date
Japan (11 Oct 2005),
MeaslesRubella
Regulation-
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Related

3
Clinical Trials associated with Freeze-Dried Live Attenuated Measles And Rubella Combined Vaccine(Takeda)
JPRN-jRCT1080222440
/ Unknown statusNot Applicable
Freeze-dried live attenuated measles and rubella combined vaccine Takeda Special drug use surveillance of vaccinees after the first vaccination
NCT02158364
/ CompletedNot Applicable
Freeze-dried Live Attenuated Measles and Rubella Combined Vaccine "Takeda" Specified Drug-use Survey of Vaccinees After the Second Vaccination
NCT02151773
/ CompletedNot Applicable
Freeze-dried Live Attenuated Measles and Rubella Combined Vaccine "Takeda" Special Drug Use Surveillance of Vaccinees After the First Vaccination
100 Clinical Results associated with Freeze-Dried Live Attenuated Measles And Rubella Combined Vaccine(Takeda)
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100 Translational Medicine associated with Freeze-Dried Live Attenuated Measles And Rubella Combined Vaccine(Takeda)
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100 Patents (Medical) associated with Freeze-Dried Live Attenuated Measles And Rubella Combined Vaccine(Takeda)
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100 Deals associated with Freeze-Dried Live Attenuated Measles And Rubella Combined Vaccine(Takeda)
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R&D Status

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Measles
Japan
Takeda Pharmaceutical Co., Ltd.Takeda Pharmaceutical Co., Ltd.
11 Oct 2005
Rubella
Japan
Takeda Pharmaceutical Co., Ltd.Takeda Pharmaceutical Co., Ltd.
11 Oct 2005
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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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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Regulation

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