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Extension Study to Assess Effects of Non-interrupted Versus Interrupted and Long Term Treatment of Two Dose Regimes of Secukinumab in Subjects With Hidradenitis Suppurativa

Phase 3
Active, not recruiting
Conditions
Hidradenitis Suppurativa
Interventions
Registration Number
NCT04179175
Lead Sponsor
Novartis Pharmaceuticals
Brief Summary

The purpose of this extension study is to evaluate maintenance of Hidradenitis Suppurativa Clinical Response (HiSCR response) in either continuous or interrupted therapy (using a randomized withdrawal period) of two dose regimens and to assess long-term efficacy, safety and tolerability of Secukinumab in subjects with moderate to severe hidradenitis suppurativa completing either of the 2 Phase III studies. This is an expanded access trial for the core trials CAIN457M2301 (NCT03713619) and CAIN457M2302 (NCT03713619).

Detailed Description

This is a multicenter extension study to both core Phase III studies CAIN457M2301 and CAIN457M2302 (Core studies). This study contains a randomized withdrawal design, double blinded and placebo controlled up to Week 104 or loss of response. The subjects with HiSCR response after 52 weeks of treatment in the "Core studies" will be randomized at 2:1 ratio to either continue on one of the two Secukinumab dosing regimens assigned in "Core studies" for another 52 weeks or will be placed on placebo. The primary endpoint is loss of response (LOR) assessed during the 52-week treatment duration (up to Week 104). Subjects who attained LOR will be transferred to open-label treatment to continue until the end of the study. Subjects on placebo who did not reach LOR up to Week 104 will be offered to continue in the open-label treatment or discontinue the study. Thus for subjects who were HiSCR responders at Week 52 of "Core studies", the open label treatment duration will vary and start either from the time of LOR or from Week 104 dose and last until Week 260 followed by 8 weeks of a post treatment follow-up period to week 268.

Subjects who were HiSCR non-responders at the end of "Core studies" will be offered to continue in open-label treatment until Week 260.

Subjects who prematurely discontinue the study, or who complete the study will enter a post-treatment follow up period (8 weeks) The primary objective is to evaluate maintenance of HiSCR response at Week 104 in either continuous or interrupted therapy compared to placebo. Secondary objectives are to assess the long-term safety and tolerability evaluated by adverse events, abnormal laboratory values and vital signs.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
703
Inclusion Criteria
  • written informed consent must be obtained before any assessment is performed
  • subject must have completed the study treatment period (52 weeks) in the core studies (AIN457M2301 or AIN457M2302) and had received secukinumab treatment during Treatment Period 2
Exclusion Criteria
  • protocol deviation in the core study which will prevent the meaningful analysis of the extension study
  • ongoing or planned use of prohibited HS or non-HS treatment
  • participation in the extension could expose the subject to an undue safety risk
  • current sever progressive or uncontrolled disease which renders the subject unsuitable for the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
secukinumab 1 HiSCR RespondersecukinumabHiSCR responder at Week 52 in core trial, secukinumab 300mg every 2 weeks
placebo 1 HiSCR RespondersecukinumabHiSCR responder at Week 52 in core trial, placebo to secukinumab 300mg every 2 weeks
secukinumab 2 HiSCR RespondersecukinumabHiSCR responder at Week 52 in core trial, secukinumab 300mg every 4 weeks
placebo 2 HiSCR RespondersecukinumabHiSCR responder at Week 52 in core trial, placebo to secukinumab 300 mg every 4 weeks
HiSCR non-responderssecukinumabnon-responder at Week 52 in core trial treatment; secukinumab 300mg every 2 weeks
Primary Outcome Measures
NameTimeMethod
Time to Loss of Response (LOR) up to Week 104 in Hidradenitis Suppurativa Clinical Response (HiSCR) RespondersUp to 52 weeks: from randomization at the extension study (Week 52) up to Week 104 or loss of response. Study day is defined with respect to the core studies.

Loss of response was defined as:

* at least a 50% increase in abscess and/or nodules (AN) count compared to the average AN count from the 3 previous visits or at Week 52, whichever is lower and the increase was at least of 3 AN.

* at least a 30% increase in AN compared to the average AN count from the 3 previous visits or Week 52, whichever is lower, with an increase of at least 2 AN and a further increase in the AN count of at least 2 AN at a re-assessment visit within 2-4 weeks

Incidence Rate of Participants Achieving Loss of Response (LOR) up to Week 104 in Hidradenitis Suppurativa Clinical Response (HiSCR) RespondersUp to 52 weeks: from randomization at the extension study (Week 52) up to Week 104 or loss of response. Study day is defined with respect to the core studies.

The incidence rate of participants achieving Loss of Response (LOR) was based on the primary estimand.

* Day 1 = Date of 1st dose intake in the extension study.

* Subjects at risk = Subjects who did not have LOR and were not censored before or at the start of the specified time interval.

* Incidence rate (%) = (number of subjects with LOR / number of subjects at risk) x 100.

Secondary Outcome Measures
NameTimeMethod
Number of Participants With Treatment Emergent Adverse EventsUp to 216 weeks: from randomization at the extension study (Week 52) up to Week 268. Study day is defined with respect to the core studies.

To assess the long-term safety and tolerability of Secukinumab in subjects with moderate to severe hidradenitis suppurativa (HS)

Trial Locations

Locations (30)

Novartis Investigative Site

🇻🇳

Ho Chi Minh, Vietnam

Skin Specialists PC

🇺🇸

Omaha, Nebraska, United States

Icahn School Of Med At Mount Sinai

🇺🇸

New York, New York, United States

Northwest Arkansas Center

🇺🇸

Rogers, Arkansas, United States

MedDerm Associates

🇺🇸

San Diego, California, United States

University Clinical Trials

🇺🇸

San Diego, California, United States

Southern California Skin and Laser

🇺🇸

Whittier, California, United States

Florida Academic Centers Research and Education LLC

🇺🇸

Coral Gables, Florida, United States

University of MiamiHealth System

🇺🇸

Miami, Florida, United States

Olympian Clinical Research

🇺🇸

Tampa, Florida, United States

University Of South Florida

🇺🇸

Tampa, Florida, United States

Advanced Medical Research

🇺🇸

Sandy Springs, Georgia, United States

Endeavor Health

🇺🇸

Glenview, Illinois, United States

Dundee Dermatology

🇺🇸

West Dundee, Illinois, United States

Dawes Fretzin Clinical Rea Group

🇺🇸

Indianapolis, Indiana, United States

Tufts Medical Center

🇺🇸

Boston, Massachusetts, United States

Beth Israel Deaconess Medical Cente

🇺🇸

Boston, Massachusetts, United States

Minnesota Clinical Study Center

🇺🇸

New Brighton, Minnesota, United States

MediSearch Clinical Trials

🇺🇸

Saint Joseph, Missouri, United States

Saint Louis University Clinical Research Unit

🇺🇸

Saint Louis, Missouri, United States

WA Uni School Of Med

🇺🇸

Saint Louis, Missouri, United States

University of North Carolina

🇺🇸

Chapel Hill, North Carolina, United States

Wright State University

🇺🇸

Fairborn, Ohio, United States

UP Medical Center H System

🇺🇸

Pittsburgh, Pennsylvania, United States

Clinical Research Ctr of Carolinas

🇺🇸

Charleston, South Carolina, United States

Bellaire Dermatology Associates

🇺🇸

Bellaire, Texas, United States

MDRI Baylor University

🇺🇸

Dallas, Texas, United States

Austin Inst for Clinical Research

🇺🇸

Pflugerville, Texas, United States

Dr. Stephen Miller, MDPA

🇺🇸

San Antonio, Texas, United States

Virginia Clinical Research

🇺🇸

Norfolk, Virginia, United States

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