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프로그램 비교

검색으로 10,000+ 프로그램 중 최대 5개를 골라 PK/PD · 독성 · 임상을 나란히 비교합니다. · 다음 갱신 D-13 · 마지막 7월 21일

현재 선택: 4 · 임상 갱신 필요 2

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV23행 · 4개 프로그램

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항목
AntibodyFDAApproved
secukinumab (Cosentyx)
Novartis·IL-17A
ORR 78.1%·t½ 31 h
AntibodystalePreclinical
Secikinumab (Secikinumab)
Novartis Pharmaceuticals·Psoriasis
2 trials
AntibodyApproved
Ixekizumab (Ixekizumab)
Eli Lilly and Company·Psoriatic Arthritis
53 trials·t½ 13 h
AntibodystalePhase 3
secukinumab (AIN457, AIN457 (secukinumab))
Novartis·Psoriatic Arthritis
ORR 53%·t½ 31 h
Overview
Program
Cosentyx (secukinumab)SecikinumabIxekizumabAIN457 (secukinumab)
Overview
Company
NovartisNovartis PharmaceuticalsEli Lilly and CompanyNovartis
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
IL-17APsoriasisPsoriatic ArthritisPsoriatic Arthritis
Overview
Indication
Psoriasis, psoriatic arthritis, ankylosing spondylitisAxial Spondylarthritis (axSpA); SecukinumabPsoriasis; Atopic DermatitisAsthma
Overview
Phase
APPROVEDPRECLINICALAPPROVEDPHASE_3
Overview
Status
APPROVEDACTIVERECRUITINGACTIVE
MoA
Mechanism
Targeted immunotherapies provide effective interventions by disrupting these cytokine-driven pathwaytargets and signaling pathwayTargeted immunotherapies provide effective interventions by disrupting these cytokine-driven pathway
MoA
Biomarker
biomarkers and optimize therapeutic strategiesbiomarkers and optimize therapeutic strategies
PK/PD
Half-life
31 h13 h31 h
PK/PD
Species
Mouse, HumanMouseRat, Human
PK/PD
Animal (cat.)
Human, MouseMouseHuman, Rat
PK/PD
Experiment
Pharmacokineticpharmacokineticpharmacokinetic
Toxicology
Species
Mouse, HumanMouseMouse, Rat, Human
Toxicology
Animal (cat.)
MouseMouseMouse
Toxicology
Major finding
Ixekizumab Treatment Persistence in Psoriatic Arthritis: Response to Joaquin et al.. We appreciate the interest of Joaquin et al in our recent study on the treatment persistence of ixekizumab in psoriatic arthritis. In response, we clarify that our study utilized prospectively collected real-world clinical data from a multicenter observational cohort, rather than administrative databases. We empha…
Clinical
Primary efficacy
ORR 78.1%ORR 53%
Clinical
PASI75
PASI 90 responders at Week 24 that secukinum
Clinical
ORR
78.10%53%
Clinical
Result source
ClinicalTrials.gov NCT04732117ClinicalTrials.gov NCT02409667
Clinical
Data Tier / Score
S · 91C · 0C · 42B · 57
Clinical
Program phase
APPROVEDPRECLINICALAPPROVEDPHASE_3
Clinical
Clinical sync
2026년 7월 18일 (3일 전)2026년 5월 22일 (61일 전 · 갱신 권장)2026년 7월 9일 (13일 전)2026년 7월 8일 (14일 전 · 갱신 권장)