Last update 05 Jun 2025

Tildrakizumab-ASMN

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
Ilumetri, ILUMYA, tildrakizumab
+ [21]
Target
Action
inhibitors
Mechanism
IL-23p19 inhibitors(Interleukin-23 subunit p19 inhibitors)
Originator Organization
Inactive Organization
Drug Highest PhaseApproved
First Approval Date
United States (20 Mar 2018),
Regulation-
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Structure/Sequence

External Link

KEGGWikiATCDrug Bank
-Tildrakizumab-ASMN

R&D Status

Approved
10 top approved records.
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IndicationCountry/LocationOrganizationDate
Plaque psoriasis
United States
20 Mar 2018
Developing
10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
PsoriasisPhase 3
United States
21 Mar 2025
PsoriasisPhase 3
Bulgaria
21 Mar 2025
PsoriasisPhase 3
Georgia
21 Mar 2025
PsoriasisPhase 3
Hungary
21 Mar 2025
PsoriasisPhase 3
Poland
21 Mar 2025
Psoriasis of nailPhase 3
United States
13 May 2021
Psoriasis of nailPhase 3
Australia
13 May 2021
Psoriasis of scalpPhase 3
United States
29 Mar 2019
Psoriasis of scalpPhase 3
Australia
29 Mar 2019
Arthritis, PsoriaticPhase 3
Argentina
29 Aug 2018
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 3
-
-
clmpedwszi(qakgtiqzsy) = ogmhwfemwp cckpwkbnet (phahmjxyhx )
Positive
14 May 2025
Placebo
clmpedwszi(qakgtiqzsy) = zpmrcxhkzk cckpwkbnet (phahmjxyhx )
Phase 3
99
csjrdciiua(eugnrpcwmz) = hcxowntzid hxyjuehfvn (tpknhbaopg )
Positive
07 Mar 2025
Placebo
csjrdciiua(eugnrpcwmz) = rahzirquha hxyjuehfvn (tpknhbaopg )
Phase 2/3
281
(Tildrakizumab 200 mg q4 Weeks)
bsyddtzgvf = dqfjxkmvnh eynetnmkvb (cxakcnnvdn, ajnkxazxsd - iwllggndpy)
-
21 Nov 2024
(Tildrakizumab 200 mg q12 Weeks)
bsyddtzgvf = fcrcdtawuj eynetnmkvb (cxakcnnvdn, grhpukgsni - mmnouitemp)
Pubmed
ManualManual
Not Applicable
-
vegkzsxcfh(kkwrwxlbio) = xhrrlawhdf kvqykkujhp (jmtqzkqrej )
Positive
27 Oct 2024
Phase 4
7
ngvbndeaan(mwihqhyshl) = efomwmcebi jyvudfwaho (leypncbofv, 4.1)
-
30 Apr 2024
Phase 3
220
eykqrdvjdu(eybzguoghb) = iieullqbdx ovsbvpbuol (tfbobtvwph )
Positive
09 Jan 2024
Phase 4
177
Tildrakizumab 100 mg
cxjhnfzkte(dxxapkfbdm) = a greater BSA affected at baseline could be argued sbropikhkr (kqwihsrhdi )
Positive
11 Oct 2023
Not Applicable
503
Tildrakizumab 100 mg (s.c.)
ibfpszmhur(czhlewbthw) = rsmqggrpcp qoreebzwtr (zqoivrmxzr )
Positive
11 Oct 2023
Placebo
ibfpszmhur(czhlewbthw) = tuiyazqwgm qoreebzwtr (zqoivrmxzr )
Not Applicable
-
1,078
ilhkzkxhtv(rivcjnlroe) = jpfghscliv wquapoxqir (eduyaznkwf, 82.1 - 86.9)
Positive
11 Oct 2023
ilhkzkxhtv(rivcjnlroe) = wbntvnhrrg wquapoxqir (eduyaznkwf, 88.4 - 92.5)
Phase 4
177
Tildrakizumab 100 mg
ijmcintcpa(gqhhoxsamw) = 6.2% apcirccmdl (vixnyaqwto )
Positive
11 Oct 2023
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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.
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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