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Extension Study up to 3 Years for Secukinumab in Psoriatic Arthritis (FUTURE 1 ext)

Primary Purpose

Psoriatic Arthritis

Status

Completed

Phase

Phase 3

Locations

International

Study Type

Interventional

Intervention

Secukinumab

Placebo

About this trial

This is an interventional treatment trial for Psoriatic Arthritis focused on measuring Extension study, psoriatic arthritis, pre-filled syringe

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Arm Label

Secukinumab 75mg

Secukinumab 150mg

Placebo - AIN457A 75mg

Placebo - AIN457 150mg

Arm Description

Subjects continued to receive secukinumab 75mg in PFS (same dose as that was received in core study CAIN457F2306) every 4 weeks up to Week 256. From Week 156, patients may have been escalated to 150 mg or 300 mg as judged appropriate by investigator

Subjects continued to receive secukinumab 150mg in PFS (same dose as that was received in core study CAIN457F2306) every 4 weeks up to Week 256. From Week 156, patients may have been escalated to 300 mg as judged appropriate by the investigator

Placebo (for maintaining the blind till Week 152): Placebo to secukinumab 0.5 mL solution solution for injection was provided in PFS for s.c. administration (a single use pre-filled 1mL long glass syringe). It contained a mixture of inactive excipients, matching the composition of secukinumab 75mg

Placebo (for maintaining the blind till Week 152): Placebo to secukinumab 1 mL solution for injection was provided in PFS for s.c. administration (a single use pre-filled 1mL long glass syringe). It contained a mixture of inactive excipients, matching the composition of secukinumab 150 mg

Outcomes

Primary Outcome Measures

Proportion of Subject Who Reached (American College of Rheumatology Score of 20) ACR20

Proportion of subjects with a positive clinical response to treatment (individual improvement) in disease activity according to ACR20 criteria if he/she has at least 20% improvement in 1. Tender 68-joint count 2. Swollen 66-joint count and 3. At least 3 of the following 5 measures: Patient's assessment of Psoriatic Arthritis (PsA) pain Patient's global assessment of disease activity Physician's global assessment of disease activity Subject self-assessed disability (Health-Assessment Questionnaire [HAQ-DI] score) Acute phase reactant (hsCRP or ESR)

Proportion of Subjects Who Reached ACR50

Proportion of subjects that have a positive clinical response to treatment (individual improvement) in disease activity according to ACR50 criteria if he/she has at least 50% improvement in 1. Tender 68-joint count 2. Swollen 66-joint count and 3. At least 3 of the following 5 measures: Patient's assessment of PsA pain Patient's global assessment of disease activity Physician's global assessment of disease activity Subject self-assessed disability (Health-Assessment Questionnaire [HAQ-DI] score) Acute phase reactant (hsCRP or ESR)

Proportion of Subjects Who Reached ACR70

Proportion of subjects that have a positive clinical response to treatment (individual improvement) in disease activity according to ACR70 criteria if he/she has at least 70% improvement in 1. Tender 68-joint count 2. Swollen 66-joint count and 3. At least 3 of the following 5 measures:- Patient's assessment of PsA pain Patient's global assessment of disease activity Physician's global assessment of disease activity Subject self-assessed disability (Health-Assessment Questionnaire [HAQ-DI] score) Acute phase reactant (hsCRP or ESR)

Secondary Outcome Measures

Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI)

Changes from baseline in score of the disability assessment component of the HAQ (Health Assessment Questionnaire - Disability Index). The HAQ-DI, assesses a subject's level of functional ability and includes questions of fine movements of the upper extremity, locomotor activities of the lower extremity, and activities that involve both upper and lower extremities. Health Assessment Questionnaire - Disability Index (HAQ-DI) ranges from 0 (no disability) to 3 (very severe disability)

Minimal Clinically Important Difference (MCID) in Health Assessment Questionnaire Disability Index (HAQ-DI)

Percentage of subjects with improvements from baseline in HAQ-DI meeting or exceeding minimal clinically important difference (MCID=0.3). The HAQ-DI, assesses a subject's level of functional ability and includes questions of fine movements of the upper extremity, locomotor activities of the lower extremity, and activities that involve both upper and lower extremities.

Change From Baseline in Disease Activity Score-CRP (DAS28)

Changes in DAS28 (utilizing hsCRP) from baseline up to Month 60. The DAS28 is a measure of disease activity in PsA based on Swollen and Tender Joint Counts (out of a total of 28), hsCRP and the Patient's Global Assessment of Disease Activity. A DAS28 score greater than 5.1 implies active disease, equal to or less than 3.2 low disease activity, and less than 2.6 remission. This measure represents change in scores - not the actual scores. DAS28 is a combined measure of disease activity based on the following formula: DAS28-CRP = 0.56*TJC28^0.5 + 0.28*SJC28^0.5 + 0.36*ln(CRP+1) + 0.014*PGA + 0.96 The greater the score is, the more the disease activity exists. Remission is defined as DAS28-CRP < 2.6 Low disease activity is defined as DAS28-CRP < 3.2 The minimum value can be 0.96 (not applicable in our study due to the inclusion/exclusion criteria regarding tender, swollen joints). There is no maximum expected value for this score

Percentage of Subjects Achieving Low Disease Activity

Percentage of subjects achieving low disease activity (DAS28 ≤ 3.2). The DAS28 is a measure of disease activity in PsA based on Swollen and Tender Joint Counts (out of a total of 28), hsCRP and the Patient's Global Assessment of Disease Activity. A DAS28 score greater than 5.1 implies active disease, equal to or less than 3.2 low disease activity, and less than 2.6 remission

Percentage of Subjects Achieving Disease Remission (DAS28<2.6)

Percentage of subjects achieving disease remission (DAS28<2.6). The DAS28 is a measure of disease activity in PsA based on Swollen and Tender Joint Counts (out of a total of 28), hsCRP and the Patient's Global Assessment of Disease Activity. A DAS28 score greater than 5.1 implies active disease, equal to or less than 3.2 low disease activity, and less than 2.6 remission

Full Information

NCT ID

NCT01892436

First Posted

July 1, 2013

Last Updated

May 20, 2019

Sponsor

Novartis Pharmaceuticals

1. Study Identification

Unique Protocol Identification Number

NCT01892436

Brief Title

Extension Study up to 3 Years for Secukinumab in Psoriatic Arthritis

Acronym

FUTURE 1 ext

Official Title

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

Study Type

Interventional

2. Study Status

Record Verification Date

May 2019

Overall Recruitment Status

Completed

Study Start Date

September 30, 2013 (Actual)

Primary Completion Date

January 11, 2018 (Actual)

Study Completion Date

January 11, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Novartis Pharmaceuticals

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Yes

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Psoriatic Arthritis

Keywords

Extension study, psoriatic arthritis, pre-filled syringe

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 3

Interventional Study Model

Parallel Assignment

Masking

ParticipantInvestigator

Allocation

Randomized

Enrollment

460 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Secukinumab 75mg

Arm Type

Experimental

Arm Description

Arm Title

Secukinumab 150mg

Arm Type

Experimental

Arm Description

Arm Title

Placebo - AIN457A 75mg

Arm Type

Experimental

Arm Description

Arm Title

Placebo - AIN457 150mg

Arm Type

Experimental

Arm Description

Intervention Type

Drug

Intervention Name(s)

Secukinumab

Other Intervention Name(s)

AIN457

Intervention Description

Secukinumab is a human monoclonal antibody. Monoclonal antibodies are proteins that recognize and bind to unique proteins that your body produces. Secukinumab binds and reduces the activity of a cytokine (a "messenger" protein in the body) called Interleukin 17 (IL-17).

Intervention Type

Drug

Intervention Name(s)

Placebo

Other Intervention Name(s)

Placebo - AIN457A

Intervention Description

Placebo

Primary Outcome Measure Information:

Title

Proportion of Subject Who Reached (American College of Rheumatology Score of 20) ACR20

Description

Time Frame