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Efficacy and Safety Study of Tildrakizumab in the Treatment of Nail Psoriasis

Primary Purpose

Chronic Plaque Psoriasis, Moderate to Severe Nail Psoriasis

Status
Recruiting
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Tildrakizumab
Placebo
Sponsored by
Sun Pharmaceutical Industries Limited
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Plaque Psoriasis

Eligibility Criteria

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

Inclusion Criteria:

Subjects are eligible to be included in the study only if all of the following criteria apply:

  1. Subjects with a chronic moderate to severe plaque-type psoriasis for at least 6 months (as determined by subject interview and confirmation of diagnosis through physical examination by Investigator).
  2. Subjects must have moderate to severe nail psoriasis at Screening and Baseline, defined by:

    • mNAPSI score of ≥20.
    • ViSENPsO ≥3
  3. Subjects must have moderate to severe plaque psoriasis at Screening and Baseline, defined by:

    • s-PGA score of at least 3.
    • Body Surface Area (BSA) involvement of ≥10%.
    • PASI ≥12
  4. Subjects must be considered candidates for systemic therapy, meaning psoriasis inadequately controlled by topical treatments (corticosteroids), and/or phototherapy, and/or previous systemic therapy.

Exclusion Criteria:

Subjects are excluded from the study if any of the following criteria apply:

  1. Subjects who have predominantly non-plaque forms of psoriasis, specifically erythrodermic psoriasis, predominantly pustular psoriasis, medication-induced, or medication-exacerbated psoriasis, or new-onset guttate psoriasis.
  2. Subjects with ongoing inflammatory skin diseases other than psoriasis or any other disease affecting the fingernails, which may potentially confound the evaluation of study treatment.
  3. Subjects with fungal nail infection should be excluded from the study. Subjects in whom the Investigator suspects a fungal nail infection in addition to nail psoriasis should have scrapings sent for direct microscopy and fungal culture. If fungal culture or direct microscopy of nail scrapings turns out to be positive for fungal infection, the subject should be excluded from the study. At the discretion of the investigator, Periodic Acid-Schiff (PAS) staining for nail clippings could also be considered to rule of fungal infection of the nails. Direct microscopy or fungal culture are not required if fungal infection is diagnosed in PAS staining.
  4. Subjects with any previous use of tildrakizumab or other IL-23/Th-17 pathway inhibitors, including p40, p19 and IL-17 antagonists for psoriasis.
  5. Subjects with known history of allergy or hypersensitivity to any of the inactive ingredients of the Tildrakizumab or placebo formulations.

Sites / Locations

  • California Dermatology & CRI (Site 13)Recruiting
  • First OC Dermatology (Site 09)Recruiting
  • Avance Trials (Site 14)
  • Dermatology Research Associates (Site 10)Recruiting
  • Clinical Science Institute (Site 05)Recruiting
  • Florida Academic Centers Research and Education, LLC (Site 07)Recruiting
  • Site 23Recruiting
  • Clinical Trials Management,LLC (Site 12)
  • Site 24
  • Forest Hills Dermatology Group (Site 01)Recruiting
  • Haber Dermatology, Inc. (Site 08)
  • Site 25
  • Oregon Dermatology and Research Center (Site 11)
  • Clinical Partners, LLC (Site 03)Recruiting
  • Center for Clinical Studies Cypress (Site 06)Recruiting
  • Center for Clinical Studies (Site 04)Recruiting
  • Progressive Clinical Research (Site 15)Recruiting
  • Center for Clinical Studies, LTD.LLP (Site 02)
  • Site 20Recruiting
  • Site 22Recruiting
  • Veracity Clinical Research/ Specialist Connect(Site 19)Recruiting
  • North Eastern Health Specialists (Site 21)Recruiting
  • Skin Health Institute Inc. (Site 18)Recruiting
  • Fremantle Dermatology (Site 16)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Arm A

Arm B

Arm Description

Outcomes

Primary Outcome Measures

The proportion of subjects who achieve at least a 75% improvement from baseline in totalmNAPSI at Week 28.
Primary Efficacy Endpoint

Secondary Outcome Measures

The proportion of subjects with a score of "0 - normal" or "1 - minimal nail psoriasis" and at least a 2-point decrease from baseline at Week 28 as measured by the ViSENPsO.
The proportion of subjects with at least 3 point decrease from baseline, in Nail Pain NRS score in subjects with baseline nail pain NRS score of >3

Full Information

First Posted
March 27, 2019
Last Updated
July 13, 2023
Sponsor
Sun Pharmaceutical Industries Limited
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1. Study Identification

Unique Protocol Identification Number
NCT03897075
Brief Title
Efficacy and Safety Study of Tildrakizumab in the Treatment of Nail Psoriasis
Official Title
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Assess the Efficacy and Safety of Tildrakizumab in the Treatment of Moderate to Severe Nail Psoriasis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 13, 2021 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sun Pharmaceutical Industries Limited

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Phase 3b study to Assess the Efficacy and Safety of Tildrakizumab in the Treatment of Moderate to Severe Nail Psoriasis

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Plaque Psoriasis, Moderate to Severe Nail Psoriasis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm A
Arm Type
Experimental
Arm Title
Arm B
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Tildrakizumab
Intervention Description
PART 1: Double-blind Placebo-controlled PART 2: Double-blind Active Treatment Extension PART 3: Observational Safety Follow-up
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
PART 1: Double-blind Placebo-controlled PART 2: Double-blind Active Treatment Extension PART 3: Observational Safety Follow-up
Primary Outcome Measure Information:
Title
The proportion of subjects who achieve at least a 75% improvement from baseline in totalmNAPSI at Week 28.
Description
Primary Efficacy Endpoint
Time Frame
Week 28
Secondary Outcome Measure Information:
Title
The proportion of subjects with a score of "0 - normal" or "1 - minimal nail psoriasis" and at least a 2-point decrease from baseline at Week 28 as measured by the ViSENPsO.
Time Frame
Week 28
Title
The proportion of subjects with at least 3 point decrease from baseline, in Nail Pain NRS score in subjects with baseline nail pain NRS score of >3
Time Frame
Week 28
Other Pre-specified Outcome Measures:
Title
The percentage of subjects with incidence, seriousness, and severity of all adverse events.
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with severe infections whether or not reported as a serious event defined as any infection meeting the regulatory definition of a serious adverse event, or any infection requiring intravenous antibiotics.
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with malignancies (excluding carcinoma in situ of the cervix).
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with non-melanoma skin cancer.
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with Major Adverse Cardiovascular Events.
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with melanoma skin cancer.
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with injection site reactions (eg. pain, erythema, edema etc)
Description
Primary Safety Endpoint
Time Frame
Week 52
Title
The percentage of subjects with study treatment related hypersensitivity reactions (eg, anaphylaxis, urticaria, angioedema, etc).
Description
Primary Safety Endpoint
Time Frame
Week 52

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects are eligible to be included in the study only if all of the following criteria apply: Subjects with a chronic moderate to severe plaque-type psoriasis for at least 6 months (as determined by subject interview and confirmation of diagnosis through physical examination by Investigator). Subjects must have moderate to severe nail psoriasis at Screening and Baseline, defined by: mNAPSI score of ≥20. ViSENPsO ≥3 Subjects must have moderate to severe plaque psoriasis at Screening and Baseline, defined by: s-PGA score of at least 3. Body Surface Area (BSA) involvement of ≥10%. PASI ≥12 Subjects must be considered candidates for systemic therapy, meaning psoriasis inadequately controlled by topical treatments (corticosteroids), and/or phototherapy, and/or previous systemic therapy. Exclusion Criteria: Subjects are excluded from the study if any of the following criteria apply: Subjects who have predominantly non-plaque forms of psoriasis, specifically erythrodermic psoriasis, predominantly pustular psoriasis, medication-induced, or medication-exacerbated psoriasis, or new-onset guttate psoriasis. Subjects with ongoing inflammatory skin diseases other than psoriasis or any other disease affecting the fingernails, which may potentially confound the evaluation of study treatment. Subjects with fungal nail infection should be excluded from the study. Subjects in whom the Investigator suspects a fungal nail infection in addition to nail psoriasis should have scrapings sent for direct microscopy and fungal culture. If fungal culture or direct microscopy of nail scrapings turns out to be positive for fungal infection, the subject should be excluded from the study. At the discretion of the investigator, Periodic Acid-Schiff (PAS) staining for nail clippings could also be considered to rule of fungal infection of the nails. Direct microscopy or fungal culture are not required if fungal infection is diagnosed in PAS staining. Subjects with any previous use of tildrakizumab or other IL-23/Th-17 pathway inhibitors, including p40, p19 and IL-17 antagonists for psoriasis. Subjects with known history of allergy or hypersensitivity to any of the inactive ingredients of the Tildrakizumab or placebo formulations.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Head, Clinical development
Phone
91 2266455645
Ext
5689
Email
Clinical.Trial@sunpharma.com
Facility Information:
Facility Name
California Dermatology & CRI (Site 13)
City
Encinitas
State/Province
California
ZIP/Postal Code
92007
Country
United States
Individual Site Status
Recruiting
Facility Name
First OC Dermatology (Site 09)
City
Fountain Valley
State/Province
California
ZIP/Postal Code
92708
Country
United States
Individual Site Status
Recruiting
Facility Name
Avance Trials (Site 14)
City
Laguna Niguel
State/Province
California
ZIP/Postal Code
92677
Country
United States
Individual Site Status
Withdrawn
Facility Name
Dermatology Research Associates (Site 10)
City
Los Angeles
State/Province
California
ZIP/Postal Code
90045
Country
United States
Individual Site Status
Recruiting
Facility Name
Clinical Science Institute (Site 05)
City
Santa Monica
State/Province
California
ZIP/Postal Code
90404
Country
United States
Individual Site Status
Recruiting
Facility Name
Florida Academic Centers Research and Education, LLC (Site 07)
City
Coral Gables
State/Province
Florida
ZIP/Postal Code
33134
Country
United States
Individual Site Status
Recruiting
Facility Name
Site 23
City
Ocala
State/Province
Florida
ZIP/Postal Code
34470
Country
United States
Individual Site Status
Recruiting
Facility Name
Clinical Trials Management,LLC (Site 12)
City
Metairie
State/Province
Louisiana
ZIP/Postal Code
70006
Country
United States
Individual Site Status
Withdrawn
Facility Name
Site 24
City
Troy
State/Province
Michigan
ZIP/Postal Code
48084
Country
United States
Individual Site Status
Withdrawn
Facility Name
Forest Hills Dermatology Group (Site 01)
City
Forest Hills
State/Province
New York
ZIP/Postal Code
11375
Country
United States
Individual Site Status
Recruiting
Facility Name
Haber Dermatology, Inc. (Site 08)
City
Beachwood
State/Province
Ohio
ZIP/Postal Code
44122
Country
United States
Individual Site Status
Withdrawn
Facility Name
Site 25
City
Mayfield Heights
State/Province
Ohio
ZIP/Postal Code
44124
Country
United States
Individual Site Status
Withdrawn
Facility Name
Oregon Dermatology and Research Center (Site 11)
City
Portland
State/Province
Oregon
ZIP/Postal Code
97210
Country
United States
Individual Site Status
Withdrawn
Facility Name
Clinical Partners, LLC (Site 03)
City
Johnston
State/Province
Rhode Island
ZIP/Postal Code
02919
Country
United States
Individual Site Status
Recruiting
Facility Name
Center for Clinical Studies Cypress (Site 06)
City
Cypress
State/Province
Texas
ZIP/Postal Code
77433
Country
United States
Individual Site Status
Recruiting
Facility Name
Center for Clinical Studies (Site 04)
City
Houston
State/Province
Texas
ZIP/Postal Code
77004
Country
United States
Individual Site Status
Recruiting
Facility Name
Progressive Clinical Research (Site 15)
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78213
Country
United States
Individual Site Status
Recruiting
Facility Name
Center for Clinical Studies, LTD.LLP (Site 02)
City
Webster
State/Province
Texas
ZIP/Postal Code
77598
Country
United States
Individual Site Status
Withdrawn
Facility Name
Site 20
City
Kogarah
State/Province
New South Wales
ZIP/Postal Code
2217
Country
Australia
Individual Site Status
Recruiting
Facility Name
Site 22
City
Kogarah
State/Province
New South Wales
ZIP/Postal Code
2217
Country
Australia
Individual Site Status
Recruiting
Facility Name
Veracity Clinical Research/ Specialist Connect(Site 19)
City
Woolloongabba
State/Province
QSLD
ZIP/Postal Code
4102
Country
Australia
Individual Site Status
Recruiting
Facility Name
North Eastern Health Specialists (Site 21)
City
Campbelltown
State/Province
South Australia
ZIP/Postal Code
5073
Country
Australia
Individual Site Status
Recruiting
Facility Name
Skin Health Institute Inc. (Site 18)
City
Carlton
State/Province
Victoria
ZIP/Postal Code
3053
Country
Australia
Individual Site Status
Recruiting
Facility Name
Fremantle Dermatology (Site 16)
City
Fremantle
State/Province
WAUS
ZIP/Postal Code
6160
Country
Australia
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

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Efficacy and Safety Study of Tildrakizumab in the Treatment of Nail Psoriasis

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