A Study Comparing Different Dosing Regimens of Ixekizumab (LY2439821) in Participants With Moderate to Severe Plaque Psoriasis (IXORA-P)
2020년 6월 10일 업데이트: Eli Lilly and Company
A Multicenter, Randomized, Double-Blind Study Comparing the Efficacy and Safety of Ixekizumab Dosing Regimens in Patients With Moderate-to-Severe Plaque Psoriasis
The main purpose of this study is to evaluate the efficacy of ixekizumab dosing regimens in participants with plaque psoriasis.
연구 개요
상태
상태
완전한
정황
정황
개입 / 치료
개입 / 치료
상세 설명
The purpose of this study is to evaluate both the safety and efficacy of ixekizumab dosing regimens.
There are 3 study periods: Screening Period, Blinded Treatment Dosing Period, and Post-Treatment Follow-Up.
연구 유형
연구 유형
중재적
등록 (실제)
등록
1257
단계
단계
- 3단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Tainan, 대만, 70166
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Taipei, 대만, 10048
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Bucheon, 대한민국, 420-717
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Pusan, 대한민국, 602-739
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Seongnam, 대한민국, 463-707
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Seoul, 대한민국, 100799
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Berlin, 독일, 10789
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Darmstadt, 독일, 64283
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Kiel, 독일, 24148
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Mahlow, 독일, 15831
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Munster, 독일, 48159
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Bucuresti, 루마니아, 011025
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Cluj Napoca, 루마니아, 400006
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Constanta, 루마니아, 900125
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Craiova, 루마니아, 200642
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Mexicali, 멕시코, 21100
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Mexico City, 멕시코, 3100
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Monterrey, 멕시코, 64060
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Morelia, 멕시코, CP 58249
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Alabama
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Birmingham, Alabama, 미국, 35205
- Total Skin and Beauty Dermatology Center PC
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California
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Anaheim, California, 미국, 92801
- Anaheim Clinical Trials, LLC
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Beverly Hills, California, 미국, 90212
- David Stoll, M.D.
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Los Angeles, California, 미국, 90045
- Dermatology Research Associates
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Sacramento, California, 미국, 95819
- Center for Dermatology and Laser Surgery
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San Diego, California, 미국, 92108
- Medical Center for Clinical Research
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San Diego, California, 미국, 92123
- University Clinical Trials, Inc.
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Santa Monica, California, 미국, 90404
- Clinical Science Institute
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Colorado
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Denver, Colorado, 미국, 80209
- Cherry Creek Research, Inc
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Florida
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Coral Gables, Florida, 미국, 33134
- Florida Academic Dermatology Centers
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DeLand, Florida, 미국, 32720
- Avail Clinical Research LLC
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Jacksonville, Florida, 미국, 32216
- Jacksonville Center for Clinical Research
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Ocala, Florida, 미국, 34471
- Renstar Medical Research
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Ormond Beach, Florida, 미국, 32174
- Ameriderm Research
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Tampa, Florida, 미국, 33624
- University of South Florida
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Georgia
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Atlanta, Georgia, 미국, 30342
- Advanced Medical Research
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Illinois
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Darien, Illinois, 미국, 60561
- University Dermatology
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Indiana
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Evansville, Indiana, 미국, 47714
- Deaconess Clinic Inc
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Indianapolis, Indiana, 미국, 46256
- Dawes Fretzin Clinical Research
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South Bend, Indiana, 미국, 46617
- The South Bend Clinic
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Kansas
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Overland Park, Kansas, 미국, 66215
- Kansas City Dermatology, PA
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Wichita, Kansas, 미국, 67207
- Heartland Research Associates
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Kentucky
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Louisville, Kentucky, 미국, 40202
- Dermatology Specialist
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Louisiana
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Lake Charles, Louisiana, 미국, 70605
- Dr. Shondra Smith MD
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Maryland
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Rockville, Maryland, 미국, 20850
- DermAssociates, P.C.
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Massachusetts
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Beverly, Massachusetts, 미국, 01915
- ActivMed Practices & Research, Inc
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Missouri
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Saint Louis, Missouri, 미국, 63117
- Central Dermatology PC
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New Hampshire
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Newington, New Hampshire, 미국, 03801
- ActivMed Practices & Research, Inc
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New Jersey
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East Windsor, New Jersey, 미국, 08520
- Psoriasis Treatment Center of Central New Jersey
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New Mexico
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Albuquerque, New Mexico, 미국, 87106-5239
- Academic Dermatology Associates
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New York
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New York, New York, 미국, 10029
- Mount Sinai School of Medicine Dermatology Clinical Trials
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Rochester, New York, 미국, 14623
- Skin Search of Rochester, Inc
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North Carolina
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Chapel Hill, North Carolina, 미국, 27516
- University of North Carolina Dermatology and Skin Cancer Center
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Wilmington, North Carolina, 미국, 28401
- PMG Research of Wilmington, LLC
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Wilmington, North Carolina, 미국, 28405
- Wilmington Dermatology Center
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Winston-Salem, North Carolina, 미국, 27103
- Piedmont Medical Research
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Ohio
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Cleveland, Ohio, 미국, 44106-5055
- University Hospitals of Cleveland
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Oklahoma
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Tulsa, Oklahoma, 미국, 74135
- Healthcare Research Consultant
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Oregon
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Portland, Oregon, 미국, 97210
- Oregon Dermatology and Research Center
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Portland, Oregon, 미국, 97223
- Oregon Medical Research Center
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Pennsylvania
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Exton, Pennsylvania, 미국, 19341
- Dermatology and Skin Surgery Center
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Pittsburgh, Pennsylvania, 미국, 15213
- University of Pittsburgh Medical Center
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Wyomissing, Pennsylvania, 미국, 19610
- Pennsylvania Regional Center for Arthritis & Osteoarthritis
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Yardley, Pennsylvania, 미국, 19067
- Yardley Dermatology
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Rhode Island
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Johnston, Rhode Island, 미국, 02919
- Clinical Partners LLC
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South Carolina
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Mount Pleasant, South Carolina, 미국, 29464
- Coastal Carolina Research Center, Inc.
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Tennessee
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Knoxville, Tennessee, 미국, 37922
- The Skin Wellness Center PC
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Texas
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Austin, Texas, 미국, 78705
- Austin Dermatology Associates
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Dallas, Texas, 미국, 75246
- Menter Dermatology Research Institute
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Houston, Texas, 미국, 77004
- Center for Clinical Studies
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Houston, Texas, 미국, 77065
- Center for Clinical Studies
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Pflugerville, Texas, 미국, 78660
- Pflugerville Dermatology Clinical Research Center
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San Antonio, Texas, 미국, 78229
- Clinical Trials of Texas, Inc.
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Webster, Texas, 미국, 77598
- Center for Clinical Studies
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Utah
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Salt Lake City, Utah, 미국, 84132
- University of Utah Medical Center
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Virginia
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Norfolk, Virginia, 미국, 23507
- Virginia Clinical Research
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Washington
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Seattle, Washington, 미국, 98101
- Dermatology Associates
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Tacoma, Washington, 미국, 98405
- MultiCare Health System
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Wenatchee, Washington, 미국, 98801
- Wenatchee Valley Hospital & Clinics
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Buenos Aires, 아르헨티나, C1425DKG
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Mendoza, 아르헨티나, 5500
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Osaka, 일본, 545-8586
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Takaoka, 일본, 9330871
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Tsu, 일본, 514-8507
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Brno, 체코, 656 91
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Novy Jicin, 체코, 741 01
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Plzen-Bory, 체코, 305-99
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Praha, 체코, 100 34
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Barrie, 캐나다, L4M 6L2
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Calgary, 캐나다, T2G 1B1
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Halifax, 캐나다, B3H1Z2
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Hamilton, 캐나다, L8N1V6
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London, 캐나다, N6A 3H7
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Markham, 캐나다, L3P1X2
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Montreal, 캐나다, H2K4L5
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Oakville, 캐나다, L6J7W5
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Peterborough, 캐나다, K9J 5K2
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Quebec, 캐나다, G1V 4X7
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Richmond Hill, 캐나다, L4B 1A5
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Sherbrooke, 캐나다, J1J 2G2
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Surrey, 캐나다, V3V 0C6
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Waterloo, 캐나다, N2J 1C4
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Windsor, 캐나다, N8W 1E6
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Bialystok, 폴란드, 15-351
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Gdansk, 폴란드, 80-546
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Kielce, 폴란드, 25-316
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Krakow, 폴란드, 30-438
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Lodz, 폴란드, 90-265
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Swidnik, 폴란드, 21-040
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Szczecin, 폴란드, 70-332
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Wroclaw, 폴란드, 51-318
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Caguas, 푸에르토 리코, 00727
- Office of Dr. Samuel Sanchez PSC
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Carolina, 푸에르토 리코, 00985
- Office of Dr. Alma M. Cruz
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Ponce, 푸에르토 리코, 00716
- Ponce School of Medicine CAIMED Center
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San Juan, 푸에르토 리코, 00909
- GCM Medical Group PSC
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San Juan, 푸에르토 리코, 00918
- Mindful Medical Research
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Budapest, 헝가리, 1238
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Debrecen, 헝가리, 4032
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Oroshaza, 헝가리, 5901
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Szolnok, 헝가리, 5000
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Benowa, 호주, 4217
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Carlton, 호주, 3053
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Darlinghurst, 호주, 2010
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Fremantle, 호주, 6160
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Phillip, 호주, 02606
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Woolloongabba, 호주, 4102
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
-
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
자격 기준
공부할 수 있는 나이
18년 이상 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
- Present with chronic plaque psoriasis for at least 6 months prior to enrollment
- At least 10% BSA of psoriasis at screening and at enrollment
- sPGA score of at least 3 and PASI score of at least 12 at screening and at enrollment
- Candidates for phototherapy and/or systemic therapy
- Participant must agree to use reliable method of birth control during the study; women must continue using birth control for at least 12 weeks after stopping treatment
Exclusion Criteria:
- Predominant pattern of pustular, erythrodermic, or guttate forms of psoriasis
- History of drug-induced psoriasis
- Cannot avoid excessive sun exposure or use of tanning booths for at least 4 weeks prior to enrollment and during the study
- Received systemic non-biologic psoriasis therapy or phototherapy within the previous 4 weeks; or had topical psoriasis treatment within the previous 2 weeks prior to enrollment
- Concurrent or recent use of any biologic agent
- Have participated in any study with ixekizumab
- Received a live vaccination within 12 weeks prior to enrollment
- Serious disorder or illness other than psoriasis
- Ongoing or serious infection within the last 12 weeks or evidence of tuberculosis
- Major surgery within 8 weeks of baseline, or will require surgery during the study
- Breastfeeding or nursing (lactating) women
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
팔의 수
6
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
실험적: 80 mg Ixekizumab Q2W
160 milligrams (mg) ixekizumab given as 2 subcutaneous (SQ) injections at baseline and then 80 mg ixekizumab given as 1 SQ injection every 2 weeks (Q2W) to week 52.
Placebo administered SQ, Q2W to maintain blind.
|
관리 SQ
Administered SQ
다른 이름들:
|
|
실험적: 80 mg Ixekizumab Q4W
160 mg ixekizumab given as 2 SQ injections at baseline and then 80 mg ixekizumab given as 1 SQ injection every 4 weeks (Q4W) to week 52.
Placebo administered SQ, Q2W to maintain blind.
|
관리 SQ
Administered SQ
다른 이름들:
|
|
실험적: 80 mg Ixekizumab Q4W/Q2W
160 mg ixekizumab given as 2 SQ injections at baseline and then 80 mg ixekizumab given as one SQ injection Q4W with step-up dosing to Q2W as needed (Q4W/Q2W step-up) to week 52.
Placebo administered SQ, Q2W to maintain blind.
|
관리 SQ
Administered SQ
다른 이름들:
|
|
실험적: 80 mg Ixekizumab Q2W Maximum Extended Enrollment (ME2) Cohort
160 mg ixekizumab given as 2 SQ injections at baseline and then 80 mg ixekizumab given as 1 SQ injection Q2W to week 52.
Placebo administered SQ, Q2W to maintain blind.
|
관리 SQ
Administered SQ
다른 이름들:
|
|
실험적: 80 mg Ixekizumab Q4W Maximum Extended Enrollment Cohort
160 mg ixekizumab given as 2 SQ injections at baseline and then 80 mg ixekizumab given as 1 SQ injection Q4W to week 52.
Placebo administered SQ, Q2W to maintain blind.
|
관리 SQ
Administered SQ
다른 이름들:
|
|
실험적: 80 mg Ixekizumab Q4W/Q2W Maximum Extended Enrollment Cohort
160 mg ixekizumab given as 2 SQ injections at baseline and then 80 mg ixekizumab given as one SQ injection Q4W with step-up dosing to Q2W as needed (Q4W/Q2W step-up) to week 52.
Placebo administered SQ, Q2W to maintain blind.
|
관리 SQ
Administered SQ
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Percentage of Participants Achieving Static Physician Global Assessment (sPGA) of (0,1)
기간: Week 52
|
The sPGA is the physician's determination of the participant's Psoriasis (Ps) lesions overall at a given time point.
Lesions were categorized by descriptions for induration, erythema, and scaling.
Participant's Ps was assessed as 0 (clear), 1 (minimal), 2 (mild), 3 (moderate), 4 (severe), or 5 (very severe).
An sPGA responder was defined as having a post-baseline sPGA score of "0" or "1" with at least a 2-point improvement from baseline.
Participants who did not meet the clinical response criteria or had missing data at Week 52 were considered non-responders for Non-Responder Imputation (NRI) analysis.
|
Week 52
|
|
Percentage of Participants Achieving 75% Improvement in Psoriasis Area and Severity Index (PASI 75)
기간: Week 52
|
The PASI combines the extent of body surface involvement in 4 anatomical regions (head, trunk, arms, and legs) and the severity of scaling, redness, and plaque induration/infiltration (thickness) in each region, yielding an overall score of 0 for no Ps to 72 for the most severe disease.
For each region the percent area of skin involved was estimated from 0 (0%) to 6 (90%-100%) and severity was estimated by clinical signs of erythema, induration and scaling with a scores range from 0 (no involvement) to 4 (severe involvement).
Each area is scored separately and the scores then combined for the final PASI.
Final PASI calculated as: sum of severity parameters for each region * area score * weighing factor [head (0.1), upper limbs (0.2), trunk (0.3), lower limbs (0.4)].
Overall scores range from 0 (no Ps) to 72 (the most severe disease).
Participants who did not meet the clinical response criteria or had missing data at Week52 were considered non-responders for NRI analysis.
|
Week 52
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Percentage of Participants Achieving sPGA (0)
기간: Week 52
|
The sPGA is the physician's determination of the participant's Ps lesions overall at a given time point.
Lesions were categorized by descriptions for induration, erythema, and scaling.
Participant's Ps was assessed as 0 (clear), 1 (minimal), 2 (mild), 3 (moderate), 4 (severe), or 5 (very severe).
An sPGA responder was defined as having a post-baseline sPGA score of "0" or "1" with at least a 2-point improvement from baseline.
Participants who did not meet the clinical response criteria or had missing data at Week 52 were considered non-responders for Non-Responder Imputation (NRI) analysis.
|
Week 52
|
|
Percentage of Participants Achieving PASI 90
기간: Week 52
|
PASI combines the extent of body surface involvement in 4 anatomical regions (head, trunk, arms, and legs) and the severity of scaling, redness, and plaque induration/infiltration (thickness) in each region, yielding an overall score of 0 for no Ps to 72 for the most severe disease.
For each region the percent area of skin involved was estimated from 0 (0%) to 6 (90%-100%) and severity was estimated by clinical signs of erythema, induration and scaling with a scores range from 0 (no involvement) to 4 (severe involvement).
Each area is scored separately and the scores then combined for the final PASI.
Final PASI calculated as: sum of severity parameters for each region * area score * weighing factor [head (0.1), upper limbs (0.2), trunk (0.3), lower limbs (0.4)].
Overall scores range from 0 (no Ps) to 72 (the most severe disease).
|
Week 52
|
|
Percentage of Participants Achieving PASI 100
기간: Week 52
|
The PASI combines the extent of body surface involvement in 4 anatomical regions (head, trunk, arms, and legs) and the severity of scaling, redness, and plaque induration/infiltration (thickness) in each region, yielding an overall score of 0 for no Ps to 72 for the most severe disease.
For each region the percent area of skin involved was estimated from 0 (0%) to 6 (90%-100%) and severity was estimated by clinical signs of erythema, induration and scaling with a scores range from 0 (no involvement) to 4 (severe involvement).
Each area is scored separately and the scores then combined for the final PASI.
Final PASI calculated as: sum of severity parameters for each region * area score * weighing factor [head (0.1), upper limbs (0.2), trunk (0.3), lower limbs (0.4)].
Overall scores range from 0 (no Ps) to 72 (the most severe disease).
|
Week 52
|
|
Change From Baseline in PASI
기간: Baseline, Week 52
|
The PASI combines the extent of body surface involvement in 4 anatomical regions (head, trunk, arms, and legs) and the severity of scaling, redness, and plaque induration/infiltration (thickness) in each region, yielding an overall score of 0 for no Ps to 72 for the most severe disease. Least Squares mean (LSmean) was calculated using Mixed-Effects Model of Repeated Measures (MMRM) analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured. |
Baseline, Week 52
|
|
Percent Improvement in PASI
기간: Baseline, Week 52
|
The PASI combines the extent of body surface involvement in 4 anatomical regions (head, trunk, arms, and legs) and the severity of scaling, redness, and plaque induration/infiltration (thickness) in each region, yielding an overall score of 0 for no Ps to 72 for the most severe disease. Least Squares mean (LSmean) was calculated using Mixed-Effects Model of Repeated Measures (MMRM) analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured. |
Baseline, Week 52
|
|
Mean Change From Baseline in Percent Body Surface Area (BSA) Involvement
기간: Baseline, Week 52
|
The percentage involvement of psoriasis on each participant's body surface area (BSA) was assessed by the investigator on a continuous scale from 0% (no involvement) to 100% (full involvement), in which 1% corresponds to the size of the participant's hand including palm, fingers and thumb. LS mean was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured. |
Baseline, Week 52
|
|
Mean Change From Baseline in Nail Psoriasis Severity Index (NAPSI) Score
기간: Baseline, Week 52
|
The NAPSI is a numeric, reproducible, objective tool for evaluation of fingernail (fn) Ps.
This scale is used to evaluate the severity of fn bed Ps and fn matrix Ps by area of involvement in the fn unit.
The fn is divided with imaginary horizontal and longitudinal lines into quadrants.
Each fn is given a score for fn bed Ps (0 to 4) and fn matrix Ps (0 to 4) depending on presence (score of 1) or absence (score of 0) of any of the features of fn bed and fn matrix Ps in each quadrant.
The NAPSI score of a fn is sum of scores in fn bed and fn matrix from each quadrant (maximum of 8).
Each fn is evaluated, then the sum of all fn equals the total NAPSI score with a range from 0 to 80 (0 indicates no Ps, 80 indicates worst Ps).
LS mean was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Mean Change From Baseline in Psoriasis Scalp Severity Index (PSSI) Score
기간: Baseline, Week 52
|
The PSSI is a physician assessment of erythema, induration and desquamation and percent of scalp that is covered with a scores range from 0 (none) to 4 (very severe).
The composite score is derived from the sum of scores for erythema, induration, and desquamation multiplied by the score recorded for the extent of the scalp area involved, 1 (<10%) to 6 (90-100%) with a total score ranging from 0 (less severity) to 72 (more severity).
LS mean change was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Mean Change From Baseline in Palmoplantar PASI (PPASI)
기간: Baseline, Week 52
|
The Palmoplantar PASI is a composite score derived from the sum scores for erythema, induration, and desquamation multiplied by a score for the extent of palm and sole area involvement, ranging from 0 (no PPASI) to 72 (most severe PPASI).
The PPASI was only assessed if participants have palmoplantar psoriasis at baseline.
LS mean was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Percentage of Participants Achieving an Itch Numeric Rating Scale (Itch NRS) ≥4 Point Reduction From Baseline
기간: Baseline, Week 52
|
The Itch NRS is a participant-administered single-item 11-point horizontal scale anchored at 0 and 10, with 0 representing "no itch" and 10 representing "worst itch imaginable."
Overall severity of a participant's itching from Ps is indicated by circling the number that best describes the worst level of itching in the past 24 hours.
Participants who did not meet the clinical response criteria or had missing data at Week 52 were considered non-responders for Non-Responder Imputation (NRI) analysis.
|
Baseline, Week 52
|
|
Percentage of Participants Achieving Dermatology Life Quality Index (DLQI) Total Score of 0 and 1 (DLQI [0,1])
기간: Week 52
|
The DLQI is a simple, participant-administered, 10 question, validated, quality-of-life questionnaire that covers 6 domains: symptoms and feelings, daily activities, leisure, work and school, personal relationships, and treatment.
Response categories include "not at all," "a lot," and "very much," with corresponding scores of 1, 2, and 3, respectively, and unanswered ("not relevant") responses scored as "0."
Totals range from 0 to 30 (less to more impairment).
Participants who did not meet the clinical response criteria or had missing data at Week 52 were considered non-responders for Non-Responder Imputation (NRI) analysis.
|
Week 52
|
|
Change From Baseline in DLQI Total Score
기간: Baseline, Week 52
|
The DLQI is a simple, participant-administered, 10 question, validated, quality-of-life questionnaire that covers 6 domains: symptoms and feelings, daily activities, leisure, work and school, personal relationships, and treatment.
Response categories include "not at all," "a lot," and "very much," with corresponding scores of 1, 2, and 3, respectively, and unanswered ("not relevant") responses scored as "0."
Totals range from 0 to 30 (less to more impairment).
LS mean change was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Change From Baseline in Itch NRS Score
기간: Baseline, Week 52
|
The Itch NRS is a participant-administered single-item 11-point horizontal scale anchored at 0 and 10, with 0 representing "no itch" and 10 representing "worst itch imaginable."
Overall severity of a participant's itching from Ps is indicated by circling the number that best describes the worst level of itching in the past 24 hours.
LS mean change from baseline in PSSI was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Change From Baseline in Skin Pain Visual Analog Scale (VAS)
기간: Baseline, Week 52
|
The pain VAS is a participant-administered single-item scale designed to measure Skin pain from Psoriasis using a 0-100 millimeter (mm) horizontal VAS.
Overall severity of participant's skin pain from Psoriasis is indicated by placing a single mark on the horizontal 100 mm scale from 0 mm (no skin pain) to 100 mm (severe skin pain).
LS mean was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Change From Baseline in European Quality of Life - 5 Dimensions 5 Level (EQ-5D-5L) VAS
기간: Baseline, Week 52
|
EQ-5D-5L is a standardized measure of health status used to provide a simple, generic measure of health for clinical and economic appraisal.
The EQ-5D-5L consists of 2 components: a descriptive system of the respondent's health and a rating of his/her current health state using a 0 (no pain) to 100mm VAS (severe pain).
LS mean was calculated using MMRM analysis including dosing regimen, country, baseline weight category, baseline value, visit, dosing regimen-by-visit, and baseline value-by-visit interactions as fixed factors, with variance-covariance structure set to unstructured.
|
Baseline, Week 52
|
|
Pharmacokinetics (PK): Trough Concentration at Steady State (Ctrough,ss) of Ixekizumab
기간: Predose, Week 4, 12, 24, 36 and 52 Post dose
|
Trough concentrations at steady state of Ixekizumab were evaluated.
|
Predose, Week 4, 12, 24, 36 and 52 Post dose
|
|
Number of Participants With Anti-Ixekizumab Antibodies
기간: Baseline through Week 52
|
Number of participants with treatment-emergent positive anti-ixekizumab antibodies was summarized by treatment group.
|
Baseline through Week 52
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작
연구 시작
2015년 8월 1일
기본 완료 (실제)
기본 완료
2016년 11월 1일
연구 완료 (실제)
연구 완료
2017년 8월 3일
연구 등록 날짜
최초 제출
최초 제출
2015년 7월 30일
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
2015년 7월 30일
처음 게시됨 (추정)
처음 게시됨
2015년 7월 31일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
2020년 6월 17일
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
2020년 6월 10일
마지막으로 확인됨
마지막으로 확인됨
2020년 6월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- 15988
- I1F-MC-RHBP (기타 식별자: Eli Lilly and Company)
- 2015-000190-12 (EudraCT 번호)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
예
IPD 계획 설명
Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.
IPD 공유 기간
Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later.
Data will be indefinitely available for requesting.
IPD 공유 액세스 기준
A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
IPD 공유 지원 정보 유형
- 연구_프로토콜
- 수액
- CSR
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .