Extension Study up to 3 Years for Secukinumab in Psoriatic Arthritis



Status:Completed
Conditions:Arthritis, Psoriasis
Therapuetic Areas:Dermatology / Plastic Surgery, Rheumatology
Healthy:No
Age Range:18 - Any
Updated:12/22/2018
Start Date:September 30, 2013
End Date:January 11, 2018

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A Three-year Extension Study to Evaluate the Long Term Efficacy, Safety and Tolerability of Secukinumab in Patients With Active Psoriatic Arthritis

This study was designed as a 3-year extension to the phase III core study CAIN457F2306. It
aimed to provide continuous treatment with secukinumab in pre-filled syringes (PFS) for
subjects who completed the core study CAIN457F2306, to obtain further long term efficacy,
safety and tolerability information in subjects with active psoriatic arthritis receiving
secukinumab every 4 weeks. At Week 104 of the study CAIN457F2306, eligible subjects completed
the assessments associated with the core study visit and subsequently continued in this
extension study on the same dose that they were receiving during the core study. The regular
assessments of disease activity ensure that subjects who are experienced worsening of disease
in any of the treatment groups could exit the study upon their own wish or based on the
advice of the investigator at any time.


Inclusion criteria

- Subjects must be able to understand and communicate with the investigator and comply
with the requirements of the study and must give a written, signed and dated informed
consent before any study assessment is performed

- Subjects must have participated in core study CAIN457F2306, and must have completed
the entire treatment period

- Subjects must be deemed by the investigator to benefit from continued secukinumab
therapy

Exclusion criteria

- Any subject taking other concomitant biologic immunomodulating agent(s) except
secukinumab

- Any subject who is deemed not to be benefiting from the study treatment based upon
lack of improvement or worsening of their symptoms

- Pregnant or nursing (lactating) women

- Women of child-bearing potential, unless they are using effective methods of
contraception during the entire study or longer if required by locally approved
prescribing information (e.g., 20 weeks in EU)

Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
25
sites
Seattle, Washington 98103
2007
mi
from 43215
Seattle, WA
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Anniston, Alabama 36207
462
mi
from 43215
Anniston, AL
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Benbrook, Texas 76126
946
mi
from 43215
Benbrook, TX
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Caba, Buenos Aires
5386
mi
from 43215
Caba,
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Charleston, South Carolina 29407
525
mi
from 43215
Charleston, SC
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Charlotte, North Carolina 28277
360
mi
from 43215
Charlotte, NC
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Columbia, South Carolina 29201
427
mi
from 43215
Columbia, SC
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Dallas, Texas 75216
914
mi
from 43215
Dallas, TX
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Dallas, Texas 75216
914
mi
from 43215
Dallas, TX
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Duncansville, Pennsylvania 16635
244
mi
from 43215
Duncansville, PA
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Eagan, Minnesota 55121
616
mi
from 43215
Eagan, MN
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Freehold, New Jersey 07728
461
mi
from 43215
Freehold, NJ
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Houston, Texas 77030
995
mi
from 43215
Houston, TX
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Houston, Texas 77030
995
mi
from 43215
Houston, TX
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Jackson, Tennessee 38305
436
mi
from 43215
Jackson, TN
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League City, Texas 77573
993
mi
from 43215
League City, TX
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Lincoln, Nebraska 68506
718
mi
from 43215
Lincoln, NE
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Mesa, Arizona 85205
1644
mi
from 43215
Mesa, AZ
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Mesa, Arizona 85205
1644
mi
from 43215
Mesa, AZ
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Mesquite, Texas 75150
901
mi
from 43215
Mesquite, TX
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Oklahoma City, Oklahoma 73104
848
mi
from 43215
Oklahoma City, OK
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Paradise Valley, Arizona 85253
1653
mi
from 43215
Paradise Valley, AZ
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Saint Louis, Missouri 63128
406
mi
from 43215
Saint Louis, MO
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Tamarac, Florida 33321
963
mi
from 43215
Tamarac, FL
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Upland, California 91786
1940
mi
from 43215
Upland, CA
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