A Study to Test the Long-term Safety of BI 655130 in Patients With Atopic Eczema Who Took Part in Study 1368-0032

Dermatitis, Atopic Clinical Trial

Official title:

An Open Label Extension Study to Assess the Long Term Safety of Treatment With BI 655130 Administered Subcutaneously in Adult Patients With Moderate to Severe Atopic Dermatitis

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04086121
• Other study ID #: 1368-0037
• Status: Terminated
• Phase: Phase 2
• Start date: September 24, 2019
• Est. completion date: February 23, 2022

Study information

• Verified date: June 2022
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess the long term safety and efficacy of treatment with BI 655130 in patients with AD who have completed and have responded to treatment in the parent study 1368-0032

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 14
• Est. completion date: February 23, 2022
• Est. primary completion date: April 28, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Signed and dated written informed consent in accordance with Good Clinical Practice (GCP) and local legislation prior to the start of any screening procedures
• Patients who completed the 1368-0032 trial and did not prematurely discontinue

treatment prior to week 16, and; In the 1368-0032 re-allocation period (V7 to V11):

• If an original non-responder from week 16 (V7), attained at least EASI 50 by last infusion (week 28) or by the EOS.
• If an original responder from week 16 (V7) completed the last visit Week 28 (EOS) or dropped to a EASI 50 score prior to Week 28.
• Women of childbearing potential (WOCBP)1 must be ready and able to use highly effective methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per year when used consistently and correctly for the duration of the trial and 16 weeks after last study drug administration. A list of contraception methods meeting these criteria is provided in the patient information.

Exclusion Criteria:

• Women who are pregnant, nursing, or who plan to become pregnant while in the trial.
• Any new documented active or suspected malignancy except appropriately treated basal cell carcinoma, squamous cell carcinoma of the skin or in situ carcinoma of uterine cervix.
• Use of any restricted medication: or any drug considered likely to interfere with the safe conduct of the study, as assessed by the investigator.
• Active systemic infections during the last two weeks prior to first drug administration.
• Currently enrolled in another investigational device or drug trial, except for 1368-0032.
• Any condition which would prevent the patient continuing on treatment in this trial 1368-0037
• Evidence of a current or previous disease, medical condition (including chronic alcohol or drug abuse or any condition) other than AD, surgical procedure, psychiatric or social problems, medical examination finding (including vital signs and ECG), or laboratory value at the screening outside the reference range that in the opinion of the investigator is clinically significant and would make the study participant unreliable to adhere to the protocol, comply with all study visits/procedures or to complete the trial, compromise the safety of the patient or compromise the quality of the data.
• History of allergy/hypersensitivity to the systemically administered trial medication agent or its excipients

Related Conditions & MeSH terms

• Dermatitis
• Dermatitis, Atopic

Intervention

Drug:
• Spesolimab
Solution for SC injection

Locations

Country	Name	City	State
Canada	Innovaderm Research Inc.	Montreal	Quebec
Japan	Tennocho Ekimae Dermatology and Allergology	Kanagawa, Yokohama
Japan	Tokyo Medical University Hachioji Medical Center	Tokyo, Hachioji
United States	Dermatology Treatment and Research Center, PA	Dallas	Texas
United States	Clinical Physiology Associates	Fort Myers	Florida
United States	Finlay Medical Research Corp	Miami	Florida
United States	Unity Clinical Research	Oklahoma City	Oklahoma
United States	The Indiana Clinical Trials Center, PC	Plainfield	Indiana
United States	CCT Research	Scottsdale	Arizona
United States	ForCare Clinical Research, Inc.	Tampa	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Countries where clinical trial is conducted

United States,  Canada,  Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Patients With Treatment Emergent Adverse Events (AEs) at Week 48	Number of patients with treatment emergent adverse events (AEs) at week 48. The treatment emergent adverse event refer to the adverse event with an onset between start of treatment and end of the 16-week residual effect period after the last dose of trial medication.	From first dose until Week 48, up to 48 weeks.
Secondary	Percentage Change From Baseline in the Eczema Area and Severity Index (EASI) Score at Week 48	The EASI scoring system is used routinely in patients with psoriasis to describe signs and severity of the disease. It assesses the extent of disease at four body sites and measures four clinical signs: erythema, induration/papulation, excoriation, and lichenification (each on a scale of 0 to 3 (0 = none, absent; 1 = mild; 2 = moderate; 3 = severe)). The EASI score was obtained by weight-averaging these 4 scores, resulting in the EASI score ranges from 0 (clear) to 72 (very severe), with higher score indicating more severe disease extent and clinical signs. The percent change from baseline in EASI is calculated as: (EASI at week 48 - EASI at baseline) / EASI at baseline * 100%.	At baseline and at Week 48.
Secondary	Percentage of Patients With a 50% Improvement From Baseline in EASI (EASI50) at Week 48	The EASI scoring system is used routinely in patients with psoriasis to describe signs and severity of the disease. It assesses the extent of disease at four body sites and measures four clinical signs: erythema, induration/papulation, excoriation, and lichenification (each on a scale of 0 to 3 (0 = none, absent; 1 = mild; 2 = moderate; 3 = severe)). The EASI score was obtained by weight-averaging these 4 scores, resulting in the EASI score ranges from 0 (clear) to 72 (very severe), with higher score indicating more severe disease extent and clinical signs. [(EASI at week 48 - EASI at baseline) / EASI at baseline * 100%] = 50%, then EASI50 = 1.	At baseline and at Week 48.
Secondary	Percentage of Patients With a 75% Improvement From Baseline in EASI (EASI75) at Week 48	The EASI scoring system is used routinely in patients with psoriasis to describe signs and severity of the disease. It assesses the extent of disease at four body sites and measures four clinical signs: erythema, induration/papulation, excoriation, and lichenification (each on a scale of 0 to 3 (0 = none, absent; 1 = mild; 2 = moderate; 3 = severe)). The EASI score was obtained by weight-averaging these 4 scores, resulting in the EASI score ranges from 0 (clear) to 72 (very severe), with higher score indicating more severe disease extent and clinical signs. [(EASI at week 48 - EASI at baseline) / EASI at baseline * 100%] = 75%, then EASI75 = 1.	At baseline and at Week 48.
Secondary	Change From Baseline in SCORing of Atopic Dermatitis (SCORAD) at Week 48	The SCORing of Atopic Dermatitis (SCORAD) index assesses elements: extent of disease, disease severity and subjective symptoms. The SCORAD consists of three elements: extent of disease, intensity of disease, and subjective symptoms (Pruritus and Sleep Loss). These 3 aspects: extent of disease (A: score range 0-1-2), disease severity (B: score range 0-18), and subjective symptoms (C: score range 0-20) combine using A/5 + 7*B/2+ C to give a maximum possible score of 103 for SCORAD score. The SCORAD range from 0 (no disease) to 103 (severe disease). The higher the SCORAD score, the more severe the Atopic Dermatitis is.	At baseline and at Week 48.
Secondary	Percentage of Patients Achieving at Least a 2-grade Reduction From Baseline to Clear (0) or Almost Clear (1) in Investigator Global Assessment (IGA) at Week 48	The IGA scale allows investigators to assess overall disease severity at one given time point, and it consists of a five-point severity scale from clear to very severe disease (0= clear,1 =almost clear, 2 = mild disease, 3 = moderate disease, 4= severe disease). The IGA scale uses clinical characteristics of erythema, infiltration, papulation, oozing and crusting as guidelines for the overall severity assessment.	At baseline and at Week 48.

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