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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05366855
Other study ID # ANB019-302
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date April 21, 2022
Est. completion date December 2026

Study information

Verified date September 2023
Source AnaptysBio, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a Phase 3, long term extension study to evaluate the safety and efficacy of imsidolimab compared with placebo in adult subjects with generalized pustular psoriasis (GPP).


Description:

This study will also evaluate the pharmacokinetic (PK) profile of imsidolimab and explore the immunogenicity of imsidolimab in subjects with GPP


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 42
Est. completion date December 2026
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Subject participated in the preceding placebo-controlled Phase 3 study ANB019-301 and completed at least the Week 1 visit of the ANB019-301 study without the use of rescue/prohibited medication for GPP - Subject must be a candidate for prolonged GPP treatment according to the Investigator's judgment Exclusion Criteria: - Use of prohibited medications between the last visit of the ANB019-301 study and the Day 1 visit of the ANB019-302 study.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Imsidolimab
Solution for infusion Solution for injection
Other:
Placebo
Solution for injection

Locations

Country Name City State
Australia Site 35-101 Melbourne
Australia Site 35102 Sydney
France Site 16-102 Nantes
France Site 16-101 Paris
Georgia Site 59104 Batumi
Georgia Site 59-101 Tbilisi
Georgia Site 59-105 Tbilisi
Georgia Site 59102 Tbilisi
Georgia Site 59103 Tbilisi
Germany Site 17102 Bensheim
Germany Site 17104 Bonn
Germany Site 17103 Hanau
Germany Site 17105 Würzburg
Korea, Republic of Site 45101 Pusan
Korea, Republic of Site 45102 Seoul
Korea, Republic of Site 45103 Seoul
Korea, Republic of Site 45104 Seoul
Malaysia Site 42104 Cheras
Malaysia Site 42-107 Johor Bahru
Malaysia Site 42106 Johor Bahru
Malaysia Site 42105 Kota Bharu
Malaysia Site 42-110 Kuala Lumpur
Malaysia Site 42101 Kuala Lumpur
Malaysia Site 42102 Muar
Malaysia Site 42-108 Pulau Pinang
Malaysia Site 42103 Putrajaya
Malaysia Site 42-109 Selayang Baru Utara
Morocco Site 64-102 Casablanca
Morocco Site 64-103 Casablanca
Morocco Site 64-101 Oujda
Poland Site 30104 Kraków
Poland Site 30105 Lódz
Poland Site 30103 Ossy
Poland Site 30101 Rzeszów
Poland Site 30102 Wroclaw
Romania Site 31-102 Bucuresti
Romania Site 31-101 Cluj-Napoca
Romania Site 31-103 Iasi
Spain Site 24-101 Barcelona
Spain Site 24-104 Las Palmas De Gran Canaria
Spain Site 24-102 Madrid
Spain Site 24-103 Madrid
Spain Site 24-105 Valencia
Taiwan Site 63101 Kaohsiung
Taiwan Site 63102 Taipei
Taiwan Site 63103 Taipei
Taiwan Site 64104 Taipei
Thailand Site 46101 Bangkok
Thailand Site 46102 Chiang Mai
Thailand Site 46104 Khon Kaen
Thailand Site 46103 Pathum Thani
Tunisia Site 62-101 Sfax
Tunisia Site 62-102 Sousse
Tunisia Site 62-103 Tunis
Turkey Site 33-101 Ankara
Turkey Site 33-103 Antalya
Turkey Site 33-105 Istanbul
Turkey Site 33-106 Istanbul
Turkey Site 33-107 Istanbul
Turkey Site 33-102 Kayseri
Turkey Site 33-104 Nilüfer
United States Site 10-101 Ann Arbor Michigan
United States Site 101 Ann Arbor Michigan
United States Site 108 Dallas Texas
United States Site 109 Largo Florida
United States Site 105 Louisville Kentucky
United States Site 102 Springville Utah

Sponsors (1)

Lead Sponsor Collaborator
AnaptysBio, Inc.

Countries where clinical trial is conducted

United States,  Australia,  France,  Georgia,  Germany,  Korea, Republic of,  Malaysia,  Morocco,  Poland,  Romania,  Spain,  Taiwan,  Thailand,  Tunisia,  Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of adverse events Incidence of adverse events Week 24
See also
  Status Clinical Trial Phase
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Recruiting NCT06013969 - A Study to Test Whether Spesolimab Helps People With Generalized Pustular Psoriasis (GPP) Who Need Treatment for Repeated Flares Phase 4
Completed NCT05512598 - HB0034 in Patients With Generalized Pustular Psoriasis (GPP) Phase 1
Active, not recruiting NCT03886246 - Effisayil™ ON: A Study to Test Long-term Treatment With Spesolimab in People With Generalized Pustular Psoriasis Who Took Part in a Previous Study Phase 2
Recruiting NCT05670821 - PMS of Spesolimab I.V. in GPP Patients With Acute Symptoms
Recruiting NCT06323356 - A Study of TAK-279 in Adult Participants With Generalized Pustular Psoriasis or Erythrodermic Psoriasis Phase 3
Completed NCT05239039 - An Expanded Access Program in China to Provide Spesolimab to People With a Flare-up in Generalized Pustular Psoriasis Who Have no Other Treatment Options Phase 3
Completed NCT04399837 - A Study to Test Whether BI 655130 (Spesolimab) Prevents Flare-ups in Patients With Generalized Pustular Psoriasis Phase 2
Completed NCT03942042 - A Study of Ixekizumab (LY2439821) in Participants in Japan With Generalized Pustular Psoriasis and Erythrodermic Psoriasis Phase 4
Completed NCT06391996 - Biologic Therapy for Generalized Pustular Psoriasis
Completed NCT03782792 - Effisayil™ 1: A Study to Test Spesolimab (BI 655130) in Patients With a Flare-up of a Skin Disease Called Generalized Pustular Psoriasis Phase 2
Completed NCT03619902 - A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Generalized Pustular Psoriasis Phase 2
Active, not recruiting NCT04566471 - Palmoplantar Pustulosis and Generalized Pustular Psoriasis: A National Population-based Analysis of Prevalence
Recruiting NCT06295692 - A Study of JNJ-77242113 for the Treatment of Participants With Generalized Pustular Psoriasis or Erythrodermic Psoriasis Phase 3
Completed NCT05200247 - An Expanded Access Trial in Japan to Provide Spesolimab to People With a Flare-up in Generalized Pustular Psoriasis Who Have no Other Treatment Options Phase 3
Completed NCT05352893 - Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With GPP Phase 3