Skip to main content
. 2022 Feb 22;22(1):e11. doi: 10.4110/in.2022.22.e11

Table 1. Clinical trials that target IL-33/ST-2.

Study title Reference Identifier Stage* Drug Disease Status
A first-in-human, double blind, single dose study in healthy subjects and subjects with mild atopic asthma (154) NCT01928368 I Astegolimab Asthma Completed
A study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of AMG 282 in healthy subjects and subjects with chronic rhinosinusitis with nasal polyps (155) NCT02170337 I Astegolimab CRS with NP Completed
A study to assess the efficacy and safety of MSTT1041A in participants with uncontrolled severe asthma (156) NCT02918019 II Astegolimab Asthma Completed
A study to assess the efficacy and safety of MSTT1041A in participants with moderate to severe atopic dermatitis (157) NCT03747575 II Astegolimab AD Completed
Anti-ST2 (MSTT1041A) in COPD (COPD-ST2OP) (158) NCT03615040 II Astegolimab COPD Completed
A study to evaluate the efficacy and safety of astegolimab in participants with chronic obstructive pulmonary disease (159) NCT05037929 II Astegolimab COPD Recruiting
A study investigating the efficacy, safety, and PK profile of ANB020 administered to adult subjects with moderate-to-severe AD (ATLAS) (160) NCT03533751 II Etokimab AD Recruiting
Proof of concept study to investigate ANB020 activity in adult patients with severe eosinophilic asthma (161) NCT03469934 II Etokimab Asthma Completed
Etokimab in adult patients with chronic rhinosinusitis with nasal polyps (CRSwNP) (162) NCT03614923 II Etokimab CRS with NP Completed
Placebo-controlled study to investigate ANB020 activity in adult patients with peanut allergy (163) NCT02920021 II Etokimab Peanut allergy Completed
A study to evaluate the safety and tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of Melrilimab (GSK3772847) in healthy participants (164) NCT04366349 I GSK3772847 Healthy/asthma Completed
Efficacy and safety study of GSK3772847 in subjects with moderately severe asthma (165) NCT03207243 II GSK3772847 Asthma Completed
Study of REGN3500 and dupilumab in patients with asthma (166) NCT03112577 I Itepekimab Asthma Completed
Study of safety, tolerability, and pharmacokinetics of multiple ascending doses of REGN3500 in adults with moderate asthma (167) NCT02999711 I Itepekimab Asthma Completed
Evaluation of SAR440340 and as combination therapy with dupilumab in moderate-to-severe asthma participants (168) NCT03387852 II Itepekimab Asthma Completed
Efficacy, safety, and pharmacokinetic profiles of REGN3500 administered to adult patients with moderate-to-severe atopic dermatitis (169) NCT03738423 II Itepekimab AD Completed
Efficacy and safety of REGN3500 monotherapy and combination of REGN3500 plus dupilumab in adult patients with moderate-to-severe atopic dermatitis (170) NCT03736967 II Itepekimab AD Terminated (Lack of efficacy)
Proof-of-concept study to assess the efficacy, safety and tolerability of SAR440340 (anti-IL-33 mAb) in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD) (171) NCT03546907 II Itepekimab COPD Completed
Study to assess the efficacy, safety, and tolerability of SAR440340/REGN3500/Itepekimab in chronic obstructive pulmonary disease (COPD) (AERIFY-1,2) (172,173) NCT04701983 III Itepekimab COPD Recruiting
NCT04751487
Safety and tolerability of MEDI3506 in healthy participants, in participants with COPD and healthy Japanese participants (174) NCT03096795 I MEDI3506 Healthy/COPD Completed
Study to assess the efficacy and safety of MEDI3506 in adults with uncontrolled moderate-to-severe asthma (FRONTIER-3) (175) NCT04570657 II MEDI3506 Asthma Recruiting
Efficacy and safety of MEDI3506 in adult subjects with atopic dermatitis (176) NCT04212169 II MEDI3506 AD Recruiting
A phase II, randomized, double-blind, placebo-controlled study to assess MEDI3506 in participants with COPD and chronic bronchitis (FRONTIER-4) (177) NCT04631016 II MEDI3506 COPD/chronic bronchitis Recruiting

NP, nasal polyp.

*Stage I, II, and III represent phase 1, phase 2, and phase 3 respectively.