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Plaque PsoriasisPhase 3Ixora-pedsNCT03073200

Study of Ixekizumab (LY2439821) in Children 6 to Less Than 18 Years With Moderate-to-Severe Plaque Psoriasis

A Phase 3 study testing Ixekizumab and Etanercept in people with Plaque Psoriasis, run by Eli Lilly and Company at 69 sites in 13 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to evaluate the safety and efficacy of ixekizumab in pediatric participants with moderate-to-severe plaque psoriasis. Read more about this study

Who is it for?
Ages 6 to 17 years
Conditions the study is for
Plaque Psoriasis
What is being tested?
Ixekizumab and Etanercept
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
201 participants
Where
69 sitesin 13 countries
Study dates
28 Mar 2017to 23 Mar 2021
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Have a diagnosis of moderate-to-severe plaque-type psoriasis for at least 6 months prior to baseline as determined by the investigator.
  • Have Psoriasis Area and Severity Index (PASI) score ≥12 and a Static Physician Global Assessment (sPGA) ≥3 and body surface area involvement ≥10% at screening and baseline.
  • Are candidates for phototherapy or systemic treatment or considered by the investigator as not adequately controlled by topical therapies.
  • Male subjects agree to use a reliable method of birth control during the study.
  • Female subjects: Participants of childbearing age or childbearing potential who are sexually active who test negative for pregnancy must be counselled and agree to use either 1 highly effective method of contraception or 2 acceptable methods of contraception combined for the duration of the study and for at least 12 weeks following the last dose of study drug, or remain abstinent during the study and for at least 12 weeks following the last dose of study drug.
  • Both the child or adolescent and a parent or legal guardian are able to understand and fully participate in the activities of the clinical study and sign their assent and consent, respectively.
  • All immunizations are up-to-date in agreement with current immunization guidelines as noted by country specific paediatric authorities (e.g., the American Academy of Paediatrics). Note, subjects who are not up to date or have never been immunized are not to be enrolled in the trial.

Who cannot join

  • Have pustular, erythrodermic, and/or guttate forms of psoriasis.
  • Have drug-induced psoriasis.
  • Have clinical and/or laboratory evidence of untreated latent or active tuberculosis (TB).
  • Participants with a documented history of immune deficiency syndrome.
  • Have any other active or recent infection, including chronic or localized infections, within 4 weeks of baseline.
  • Subjects with a known history of malignancy, lymphoproliferative disease, including lymphoma, or signs and symptoms suggestive of possible lymphoproliferative disease, such as lymphadenopathy and/or splenomegaly unless ruled out by biopsy.
Show all 10Show fewer
  • Have used any therapeutic agent targeted at reducing interleukin-17.
  • Have received other therapies within the specified time frames prior to screening (see below):
  • adalimumab and infliximab 60 days, abatacept 90 days, anakinra 7 days, or any other biologic disease-modifying antirheumatic drug 5 half-lives.
  • systemic therapy for psoriasis and psoriatic arthritis (PsA) (other than above, eg, methotrexate, cyclosporine), phototherapy (eg, photochemotherapy [psoralen plus ultraviolet A]) in the previous 4 weeks.

Trial locations and contacts

69 sites in 13 countries.

69 sites in 13 countries

United States25 sites
  • University of Alabama at Birmingham

    Birmingham, Alabama, 35233

  • University of North Carolina Dermatology and skin Cancer Cen

    Chapel Hill, North Carolina, 27516

  • Medical University of South Carolina

    Charleston, South Carolina, 29425

  • Northwestern University

    Chicago, Illinois, 60611

  • University of Chicago Medical Center

    Chicago, Illinois, 60637

  • Olympian Clinical Research

    Clearwater, Florida, 33756

  • University of Missouri

    Columbia, Missouri, 65212

  • Modern Research Associates PLLC

    Dallas, Texas, 75231

  • Psoriasis Treatment Center of Central New Jersey

    East Windsor, New Jersey, 08520

  • Dermatology and Skin Surgery Center

    Exton, Pennsylvania, 19341

  • Wright State Physicians Dermatology

    Fairborn, Ohio, 45324

  • Tien Q. Nguyen, MD inc. DBA First OC Dermatology

    Fountain Valley, California, 92708

  • Ohio State Univ College Of Medicine

    Gahanna, Ohio, 43230

  • Solutions Through Advanced Research, Inc.

    Jacksonville, Florida, 32256

  • Virginia Clinical Research

    Norfolk, Virginia, 23502

  • Oregon Dermatology and Research Center

    Portland, Oregon, 97210

  • Oregon Health and Science University

    Portland, Oregon, 97239

  • Arlington Dermatology

    Rolling Meadows, Illinois, 60008

  • Texas Dermatology and Laser Specialists

    San Antonio, Texas, 78218

  • Advanced Medical Research

    Sandy Springs, Georgia, 30328

  • The South Bend Clinic

    South Bend, Indiana, 46617

  • SSM Health Cardinal Glennon Children's Hospital

    St Louis, Missouri, 63104

  • University of South Florida

    Tampa, Florida, 33612

  • Forward Clinical Trials, Inc

    Tampa, Florida, 33624

  • Children's National Medical Center

    Washington D.C., District of Columbia, 20010

Other trials in United States

Czechia6 sites
  • Detska fakultni nemocnice

    Brno, 613 00

  • Fakultni nemocnice Hradec Kralove

    Hradec Králové, 500 05

  • Fakultni Nemocnice Plzen

    Plzen-Bory, 305 99

  • Fakultni nemocnice Kralovske Vinohrady

    Prague, 100 34

  • LF UK - Fakultni poliklinika

    Prague, 120 00

  • Nemocnice Na Bulovce

    Prague, 180 81

Other trials in Czechia

Germany5 sites
  • ISA GmbH

    Berlin, 10789

  • Universitätsklinikum Erlangen

    Erlangen, Bavaria, 91054

  • Klinikum der Johann Wolfgang Goethe-Universität Frankfurt

    Frankfurt am Main, Hesse, 60590

  • Universitätsmedizin der Johannes Gutenberg-Universität Mainz

    Mainz, Rhineland-Palatinate, 55131

  • Universitätsklinikum Münster

    Münster, North Rhine-Westphalia, 48149

Other trials in Germany

Hungary5 sites
  • Szent Janos Korhaz es Eszak-budai Egyesitett Korhazak

    Budapest, 1123

  • Debreceni Egyetem Klinikai Kozpont Borgyogyaszati Klinika

    Debrecen, Hajdú-Bihar, 4032

  • Oroshaza Varosi Onkormanyzat Korhaza

    Orosháza, 5901

  • SZTE AOK Borgyogyaszati es Allergologiai Klinika

    Szeged, Csongrád megye, 6720

  • Allergo-Derm Bakos Kft

    Szolnok, Jász-Nagykun-Szolnok, 5000

Other trials in Hungary

Argentina4 sites
  • Instituto de Neumonología y Dermatología

    Buenos Aires, C1425BEA

  • Psoriahue Medicina Interdisciplinaria

    Buenos Aires, C1425DKG

  • Centro de Investigaciones Metabólicas (CINME)

    Ciudad Autonoma de Buenos Aire, Buenos Aires, C1056ABJ

  • Fundación Estudios Clínicos- Servicio de Dermatología

    Rosario, Santa Fe Province, 5200

Other trials in Argentina

Canada4 sites
  • Institute for Skin Advancement

    Calgary, Alberta, T3A 2N1

  • Lynderm Research Inc

    Markham, Ontario, L3P1X2

  • Hospital Ste Justine

    Montreal, Quebec, H3T 1C5

  • K. Papp Clinical Research Inc

    Waterloo, Ontario, N2J 1C4

Other trials in Canada

Mexico4 sites
  • RM Pharma Specialists S.A. de C.V.

    Distrito Federal, 3100

  • Hospital Infantil de Mexico

    Mexico City, Federal District, 06720

  • Hospital Univ. Dr. Jose Eleuterio Gonzalez

    Monterrey, Nuevo León, 64460

  • Arke Estudios Clinicos S.A. de C.V.

    Veracruz, 91910

Other trials in Mexico

Puerto Rico4 sites
  • Office of Dr. Samuel Sanchez PSC

    Caguas, PR, 00727

  • Grupo Dermatologico de Carolina

    Carolina, PR, 00985

  • Ponce School of Medicine CAIMED Center

    Ponce, PR, 00716

  • GCM Medical Group PSC

    San Juan, 00917

Other trials in Puerto Rico

France3 sites
  • Centre hospitalier universitaire Pellegrin

    Bordeaux, 33076

  • Hôpital Femme Mère Enfant

    Bron, 69500

  • CHU de Nice Hopital de L'Archet

    Nice, 06202

Other trials in France

Poland3 sites
  • "Dermed" Centrum Medyczne Sp. z o.o.

    Lodz, 90-265

  • Centralny Szpital Kliniczny MSW

    Warsaw, 02-507

  • DermMEDICA Sp. z o.o.

    Wroclaw, 51-318

Other trials in Poland

Spain3 sites
  • Hospital Sant Joan de Déu

    Esplugues de Llobregat, Barcelona, 08950

  • Hospital Universitario 12 de Octubre

    Madrid, 28041

  • Hospital Universitario La Paz

    Madrid, 28046

Other trials in Spain

Russia2 sites
  • GBUZ Clinical dermatology and venereological dispensary

    Krasnodar, 350000

  • Center of Children's Health

    Moscow, 119991

Other trials in Russia

Netherlands1 site
  • Universitair Medisch Centrum St Radboud Nijmegen

    Nijmegen, 6525 GL

Other trials in Netherlands

About this study

Official title: Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate Safety, Tolerability, and Efficacy of Ixekizumab in Patients From 6 to Less Than 18 Years of Age With Moderate-to-Severe Plaque Psoriasis

The purpose of this study is to evaluate the safety and efficacy of ixekizumab in pediatric participants with moderate-to-severe plaque psoriasis.

Being tested
Ixekizumab, Placebo, Etanercept
Keywords
children, psoriasis treatment, adolescents

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • IxekizumabDrug

    Also called LY2439821

    Administered SC

  • PlaceboDrug

    Administered SC

  • EtanerceptDrug

    Administered SC

Study groups in NCT03073200
Study groupRoleWhat they receive
IxekizumabExperimentalIxekizumab given subcutaneously (SC) during the double-blind treatment period and the open-label maintenance period.
Receives: Drug: Ixekizumab
PlaceboPlacebo comparatorPlacebo given SC during the double-blind treatment period and then ixekizumab given SC during the open-label maintenance period.
Receives: Drug: Placebo
Open-Label EtanerceptExperimentalEtanercept given SC during the double-blind treatment period and then ixekizumab given SC during the open-label maintenance period. Participants will only be randomized to etanercept in countries where it is approved for severe pediatric psoriasis treatment.
Receives: Drug: Etanercept

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of Participants With a ≥75% Improvement in Psoriasis Area and Severity Index (PASI 75) (Placebo and Ixekizumab)

    PASI combines assessments of the extent of body surface involvement in 4 regions (head \& neck(h), trunk(t), arms(u), legs(l)) \& severity of scaling (S), redness (R), \& plaque induration/infiltration (thickness, T) in each region. Severity is rated for each index (R, S, T) on a 0-4 scale (0 for no involvement up to 4 for severe involvement): 0 = none, 1 = slight, 2 = mild, 3 = moderate, 4 = severe Fraction of total body surface area (BSA) affected is graded on a 0-6 scale (0 for no involvement to 6 for 90% - 100% involvement): 0 = 0% (clear), 1 = >0% to <10%, 2 = 10% to <30%, 3 = 30% to <50%, 4 = 50% to <70%, 5 = 70% to 90%, 6 = 90% to 100%.

    Overall score ranges from 0 (no psoriasis) to 72 (most severe disease).

    Measured: Week 12

  2. Percentage of Participants With a Static Physician Global Assessment (sPGA) (0,1) (Placebo and Ixekizumab)

    Static Physician Global Assessment (sPGA): The physician's global assessment of the Participant's psoriasis lesions at a given time point. Plaques are assessed for induration, erythema, and scaling, and an overall rating of psoriasis severity is given using the anchors of clear (0), minimal (1), mild (2), moderate (3), severe (4), or very severe (5). An sPGA assessed as either 0 or 1 represents a clinically meaningful response of minimal plaque severity or complete resolution of plaque psoriasis.

    Measured: Week 12

Secondary outcomes (14)
  1. Percentage of Participants With a ≥90% Improvement in Psoriasis Area and Severity Index (PASI 90)

    PASI combines assessments of the extent of body surface involvement in 4 regions (head \& neck(h), trunk(t), arms(u), legs(l)) \& severity of scaling (S), redness (R), \& plaque induration/infiltration (thickness, T) in each region. Severity is rated for each index (R, S, T) on a 0-4 scale (0 for no involvement up to 4 for severe involvement): 0 = none, 1 = slight, 2 = mild, 3 = moderate, 4 = severe Fraction of total BSA affected is graded on a 0-6 scale (0 for no involvement to 6 for 90% - 100% involvement): 0 = 0% (clear), 1 = >0% to <10%, 2 = 10% to <30%, 3 = 30% to <50%, 4 = 50% to <70%, 5 = 70% to 90%, 6 = 90% to 100%.Overall score ranges from 0 (no psoriasis) to 72 (most severe disease).

    Measured: Week 12

  2. Percentage of Participants With a sPGA (0)

    Static Physician Global Assessment (sPGA): The physician's global assessment of the Participant's psoriasis lesions at a given time point. Plaques are assessed for induration, erythema, and scaling, and an overall rating of psoriasis severity is given using the anchors of clear (0), minimal (1), mild (2), moderate (3), severe (4), or very severe (5). An sPGA assessed as either 0 or 1 represents a clinically meaningful response of minimal plaque severity or complete resolution of plaque psoriasis.

    An sPGA assessed as 0 represents a clinically important endpoint indicating complete resolution of plaque psoriasis.

    Measured: Week 12

  3. Percentage of Participants With a 100% Improvement in Psoriasis Area and Severity Index (PASI 100)

    PASI combines assessments of the extent of body surface involvement in 4 regions (head \& neck(h), trunk(t), arms(u), legs(l)) \& severity of scaling (S), redness (R), \& plaque induration/infiltration (thickness, T) in each region. Severity is rated for each index (R, S, T) on a 0-4 scale (0 for no involvement up to 4 for severe involvement): 0 = none, 1 = slight, 2 = mild, 3 = moderate, 4 = severe Fraction of total BSA affected is graded on a 0-6 scale (0 for no involvement to 6 for 90% - 100% involvement): 0 = 0% (clear), 1 = >0% to <10%, 2 = 10% to <30%, 3 = 30% to <50%, 4 = 50% to <70%, 5 = 70% to 90%, 6 = 90% to 100%.

    Overall score ranges from 0 (no psoriasis) to 72 (most severe disease).

    Measured: Week 12

  4. Percentage of Participants With a ≥75% Improvement in Psoriasis Area and Severity Index (PASI 75)

    PASI combines assessments of the extent of body surface involvement in 4 regions (head \& neck(h), trunk(t), arms(u), legs(l)) \& severity of scaling (S), redness (R), \& plaque induration/infiltration (thickness, T) in each region. Severity is rated for each index (R, S, T) on a 0-4 scale (0 for no involvement up to 4 for severe involvement): 0 = none, 1 = slight, 2 = mild, 3 = moderate, 4 = severe Fraction of total BSA affected is graded on a 0-6 scale (0 for no involvement to 6 for 90% - 100% involvement): 0 = 0% (clear), 1 = >0% to <10%, 2 = 10% to <30%, 3 = 30% to <50%, 4 = 50% to <70%, 5 = 70% to 90%, 6 = 90% to 100%. Overall score ranges from 0 (no psoriasis) to 72 (most severe disease).

    Measured: Week 4

  5. Percentage of Participants With a Static Physician Global Assessment (sPGA) (0,1)

    Static Physician Global Assessment (sPGA): The physician's global assessment of the Participant's psoriasis lesions at a given time point. Plaques are assessed for induration, erythema, and scaling, and an overall rating of psoriasis severity is given using the anchors of clear (0), minimal (1), mild (2), moderate (3), severe (4), or very severe (5). An sPGA assessed as either 0 or 1 represents a clinically meaningful response of minimal plaque severity or complete resolution of plaque psoriasis.

    Measured: Week 4

  6. Percentage of Participants With an Improvement of ≥4 in Those Who Had a Baseline Itch Numeric Rating Scale (NRS) Score of ≥4

    Itch Numeric Rating Scale (NRS): is a single-item, patient-reported outcome (PRO) measure designed to capture the overall severity of a participant's itching due to his/her psoriasis by having the patient circle the integer that describes the worst level of itching in the past 24 hours on an 11-point NRS anchored at 0 representing "no itching" and 10 representing "worst itch imaginable.

    Measured: Week 12

  7. Percentage of Participants Achieving Children's Dermatology Life Quality Index (CDLQI)/Dermatology Life Quality Index (DLQI) (0/1)

    DLQI is a validated, dermatology-specific, patient reported measure that evaluates participant's health-related quality of life. It consists of 10 items that are grouped in 6 domains: symptoms \& feelings, daily activities, leisure, work \& school , personal relationships, \& treatment. The recall period of this scale is over the "last week." Response categories and corresponding scores are:

    Very much = 3, A lot = 2, A little = 1, Not at all = 0, Not relevant = 0. A DLQI total score is calculated by summing all 10 items responses, and has a range of 0 to 30 (higher scores are indicative of greater impairment). CDLQI questionnaire is designed for use in children (4 to 16 years of age). It consists of 10 items that are grouped into 6 domains: symptoms \& feelings, leisure, school or holidays, personal relationships, sleep, \& treatment. A CDLQI total score is calculated by summing all 10 items responses, and has a range of 0 to 30 (higher scores are indicative of greater impairment).

    Measured: Week 12

  8. Change From Baseline on the Nail Psoriasis Severity Index (NAPSI)

    NAPSI is a numeric, reproducible, objective tool for evaluation of nail psoriasis. This scale was used to evaluate the severity of nail bed psoriasis \& nail matrix psoriasis by area of involvement in the nail unit. Both fingernail \& toenail involvement were assessed.The nail is divided with imaginary horizontal \& longitudinal lines into quadrants. Each nail is given a score for nail bed psoriasis (0 to 4) \& nail matrix psoriasis (0 to 4), depending on the presence (score of 1) or absence (score of 0) of any of the features of nail bed \& nail matrix psoriasis in each quadrant:

    0 = None

    1. = present in one quadrant of nail
    2. = present in two quadrants of nail
    3. = present in three quadrants of nail
    4. = present in four quadrants of nail NAPSI score of a nail is the sum of scores in nail bed \& nail matrix from each quadrant (maximum of 8). Each nail is evaluated, \& the sum of all the fingernails and toenails is the total NAPSI score ranging from 0 to 160 (No to Severe nail Psoriasis)

    Measured: Baseline, Week 12

  9. Change From Baseline on the Psoriasis Scalp Severity Index (PSSI)

    The scalp was assessed for erythema (redness), induration (hardness), and desquamation (shedding of skin) and percentage of area affected as follows:

    Erythema, Induration and Desquamation:

    0 = Absent

    1. = Slight
    2. = Moderate
    3. = Severe
    4. = Severest Possible

    Percent of Scalp Involved:

    1. = <10%
    2. = 10% - 29%
    3. = 30% - 49%
    4. = 50% - 69%
    5. = 70% - 89%
    6. = 90% - 100%

    The PSSI score is a composite score derived from the sum of the scores for erythema, induration and desquamation multiplied by the score for the extent of scalp area involved (percent of scalp involved). The range is 0 (no psoriasis) to 72 (Most severe Disease).

    LSMean was calculated using treatment, region, baseline sPGA score, baseline weight category, baseline value, visit, treatment-by-visit, and baseline-by-visit interactions as fixed factors.

    Measured: Baseline, Week 12

  10. Change From Baseline on the Palmoplantar Psoriasis Severity Index (PPASI)

    PPASI was used if the participant has palmoplantar psoriasis at baseline. Both the palms \& soles on each hand \& foot was assessed for erythema, induration, desquamation \& percentage of area affected as follows:

    Erythema (E), Induration (I), \& Desquamation (D):0 = None, 1 = Slight, 2 = Moderate, 3 = Severe, 4 = Very Severe

    Percent of Palm and Sole Area Covered:

    0 = None, 1 = <10%, 2 = 10% - 29%, 3 = 30% - 49%, 4 = 50% - 69%, 5 = 70% - 89%, 6 = 90% - 100% PPASI score is a composite score derived from the sum scores for E, I, \& D multiplied by a score for the extent of palm \& sole area involvement. The range is 0 (no psoriasis) to 72 (most severe disease).

    Measured: Baseline, Week 12

  11. Number of Participants With Anti-Ixekizumab Antibodies

    A treatment emergent - antidrug antibody (TE-ADA) positive participant were defined as:

    1. a participant with a >= 4-fold increase over a positive baseline antibody titer; or
    2. for a negative baseline titer, a participant with an increase from the baseline to a level of >= 1:10.

    Measured: Baseline through Week 48

  12. Pharmacokinetics (PK): Trough Ixekizumab Concentration at Steady State (Ctrough ss)

    Pharmacokinetics (PK): Trough Ixekizumab Concentration at Steady State (Ctrough ss).

    Measured: Week 12

  13. Percentage of Participants With a ≥75% Improvement in Psoriasis Area and Severity Index (PASI 75) (Etanercept Approved Countries)

    PASI combines assessments of the extent of body surface involvement in 4 regions (head \& neck(h), trunk(t), arms(u), legs(l)) \& severity of scaling (S), redness (R), \& plaque induration/infiltration (thickness, T) in each region. Severity is rated for each index (R, S, T) on a 0-4 scale (0 for no involvement up to 4 for severe involvement): 0 = none, 1 = slight, 2 = mild, 3 = moderate, 4 = severe Fraction of total BSA affected is graded on a 0-6 scale (0 for no involvement to 6 for 90% - 100% involvement): 0 = 0% (clear), 1 = >0% to <10%, 2 = 10% to <30%, 3 = 30% to <50%, 4 = 50% to <70%, 5 = 70% to 90%, 6 = 90% to 100%.

    Overall score ranges from 0 (no psoriasis) to 72 (most severe disease).

    Measured: Week 12

  14. Percentage of Participants With a Static Physician Global Assessment (sPGA) (0,1) (Etanercept Approved Countries)

    Static Physician Global Assessment (sPGA): The physician's global assessment of the Participant's psoriasis lesions at a given time point. Plaques are assessed for induration, erythema, and scaling, and an overall rating of psoriasis severity is given using the anchors of clear (0), minimal (1), mild (2), moderate (3), severe (4), or very severe (5). An sPGA assessed as either 0 or 1 represents a clinically meaningful response of minimal plaque severity or complete resolution of plaque psoriasis.

    Measured: Week 12

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Mar 2017
  2. Study start28 Mar 2017
  3. Primary completion7 Feb 2019
  4. Study completion23 Mar 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
201 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03073200
Sponsor's protocol ID
16367
Other IDs
I1F-MC-RHCD, 2016-003331-38, 2016
Acronym
Ixora-peds
Status last verified
16 Aug 2021
First submitted
3 Mar 2017
Last updated
27 Sep 2021
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: 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.

Publications

  • Paller AS, Seyger MMB, Magarinos GA, Pinter A, Cather JC, Rodriguez-Capriles C, Zhu D, Somani N, Garrelts A, Papp KA; IXORA-PEDS Investigators. Long-term Efficacy and Safety of Up to 108 Weeks of Ixekizumab in Pediatric Patients With Moderate to Severe Plaque Psoriasis: The IXORA-PEDS Randomized Clinical Trial. JAMA Dermatol. 2022 May 1;158(5):533-541. doi: 10.1001/jamadermatol.2022.0655.

    PubMed 35416908

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Ixekizumab and Etanercept in people with Plaque Psoriasis, run by Eli Lilly and Company at 69 sites in 13 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Sep 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 69 sites in United States, Czechia, Germany, Hungary, Argentina and 8 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 17 Mar 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of Participants With a ≥75% Improvement in Psoriasis Area and Severity Index (PASI 75) (Placebo and Ixekizumab) (time frame: Week 12). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03073200, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Sep 2021.

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