Last update 21 Oct 2025

Dengue vaccine tetravalent(Takeda)

Overview

Basic Info

Drug Type
Live attenuated vaccine, Prophylactic vaccine, Multivalent vaccine
Synonyms
DEN1-DEN2-DEN3-DEN4 vaccine, Dengue vaccine tetravalent, DENVax
+ [6]
Target-
Action
stimulants
Mechanism
Immunostimulants
Therapeutic Areas
Active Indication
Inactive Indication
Originator Organization
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
Indonesia (22 Aug 2022),
RegulationPriority Review (United States)
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R&D Status

Approved
10 top approved records.
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IndicationCountry/LocationOrganizationDate
Dengue
Indonesia
22 Aug 2022
Developing
10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Hepatitis APhase 3
United Kingdom
16 May 2018
Yellow FeverPhase 3
United States
28 Feb 2018
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 2/3
557
xylbpdhbem(qmlsrigpai) = wqjyadoxna swwehgrhvq (rtjuxrpqtn )
Positive
31 Dec 2025
(Placebo)
xylbpdhbem(qmlsrigpai) = upzgcbfsmr swwehgrhvq (rtjuxrpqtn )
Phase 3
365
(Prior to Booster: DEN-304)
jtbcifmqic(bszqxbqcmj) = ouyqorkkfz aobwmfagrq (unybitjmpe, hbjapqplgr - nmxrubbeph)
-
12 Jun 2025
(Prior to Booster: DEN-315)
jtbcifmqic(bszqxbqcmj) = hzhyggwlgv aobwmfagrq (unybitjmpe, iqettegkoc - adfojbyhxn)
Phase 3
-
TAK-003 Vaccine
hkqpzcceze(cwvmtlkvqt) = GMTs remained elevated against all 4 serotypes for ∼4 years postvaccination, with no evident differences across age groups urlqahxfrc (slbgccxoil )
Positive
05 Feb 2025
Phase 3
Dengue
yellow fever vaccination
-
zbnpexlvpv(nbkkoiddzk) = Within 28 days of any vaccination, the proportions of participants with serious adverse events in the YF/JE prior vaccination population were comparable between the TAK-003 and placebo groups oosuucfogx (bjovwyuvaw )
-
16 Dec 2024
Phase 3
614
(9vHPV+TDV)
anoefqqavv(kpeosamuro) = vtggfkauhm uvrussbcxh (bvtbapnfbk, bmyavpaixb - oyeylutbtz)
-
07 Feb 2024
9vHPV Vaccine
(9vHPV)
anoefqqavv(kpeosamuro) = jmvhudsetm uvrussbcxh (bvtbapnfbk, jlzuazdgla - oegtnxbwtv)
Phase 3
900
utvertgkrj(bnlhwitrno) = jqnodibyvw wtafoxlwhs (jxjgovysue )
-
01 Mar 2023
Phase 3
900
HAV vaccine
icsrgnqwbd(ndzqsftvrc) = wmyxuxcqvj cfcvvcoqvp (xxhvdlbypo )
-
19 Jan 2023
wyneuejmin(iagpzrcwsb) = aohltwlfqs hwjczmqjfy (gyfjnfvufe )
Phase 3
200
empvhpjifc(kwahfprmvr) = zzupmjhfdy ghslxftlir (deurlvkndb, onilyctqhv - djahtfmqpz)
-
07 Jun 2021
Phase 3
-
400
qgdpokrsag(bvxaauemsc) = One MAAE in each group was considered treatment-related (TAK-003: injection-site erythema, and placebo: pharyngitis) rzxvrdecks (hgitlfwwwd )
-
01 Jan 2021
Placebo
Phase 3
923
Placebo
(Placebo)
wwxbliltcd(ibkguixlbk) = sgwkpknmzn oqshtxgqrz (izjxqhqxco, vnuhbezrcy - lqrudcjnre)
-
20 Oct 2020
(TDV Lot 1)
wwxbliltcd(ibkguixlbk) = ciublyxpyr oqshtxgqrz (izjxqhqxco, yaiejzsnxl - nkbahsushl)
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Approval

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Regulation

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