Efficacy and Safety of Tildrakizumab Compared to Placebo in Subjects With Active Psoriatic Arthritis I (INSPIRE 1)

Study Purpose

This is a multicenter Phase III, Randomized, Double-Blind, Single-Dose, Placebo-Controlled Study to Demonstrate the Efficacy and Safety of tildrakizumab in Subjects with Active Psoriatic Arthritis I (INSPIRE 1)

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

1. Subject has provided written informed consent. 2. Subject is ≥ 18 years of age at time of Screening. 3. RF and anti-CCP Ab negative. 4. Subjects must have prior exposure to anti-TNF agent(s) use for the treatment of PsO or PsA.

Exclusion Criteria:

1. Subject has a planned surgical intervention between Baseline and the Week 24 evaluation for a pretreatment condition. 2. Subject has an active infection or history of infections as follows:
  • - any active infection for which systemic anti-infectives were used within 28 days prior to first IMP dose, with the last dose having been received within 7 days of Screening, - a serious infection, defined as requiring hospitalization or IV anti-infectives within 8 weeks prior to the first IMP dose, with the last dose having been received within 7 days of Screening, - recurrent or chronic infections, e.g., chronic pyelonephritis, chronic osteomyelitis, bronchiectasis, or other active infection that, in the opinion of the Investigator, might cause this study to be detrimental to the subject.
3. Subject has a known history of infection with hepatitis B, hepatitis C, or human immunodeficiency virus. 4. Subject had myocardial infarction, unstable angina pectoris, or ischemic stroke within the past 6 months prior to the first IMP dose. 5. Subject has any active malignancy, including evidence of cutaneous basal or squamous cell carcinoma or melanoma. 6. Subject has a history of malignancy within 5 years from the time of Screening EXCEPT treated and considered cured cutaneous basal or squamous cell carcinoma, in situ cervical carcinoma, OR in situ breast ductal carcinoma. 7. Subjects with a history of alcohol or drug abuse in the previous 2 years. 8. Female subjects of childbearing potential who do not agree to abstain from heterosexual activity or practice a dual method of contraception, for example, a combination of the following:
  • (1) oral contraceptive, depo progesterone, or intrauterine device; and (2) a barrier method (condom or diaphragm).
Male subjects with female partners of childbearing potential who are not using birth control as described above must use a barrier method of contraception (e.g., condom) if not surgically sterile (i.e., vasectomy). Contraceptive methods must be practiced upon entering the study and through 16 weeks after the last dose of IMP. If a subject discontinues prematurely, the contraceptive method must be practiced for 16 weeks following final administration of IMP. A FSH test should be performed to confirm menopause for those women with no menses for less than 1 year. 9. Subject currently enrolled in another investigational device/procedure or drug study, or Baseline of this study is less than 30 days or 5 half-lives (whichever is longer) since ending another investigational device/procedure or drug study(s), or receiving other investigational agent(s). 10. Subject previously has been enrolled (randomized) in this study. 11. Subject has any kind of disorder that, in the opinion of the Investigator, may compromise the ability of the subject to give written informed consent and/or to comply with all required study procedures. 12. Donation or loss of 400 mL or more of blood within 8 weeks before dosing. 13. Subjects who have been placed in an institution on official or judicial orders. 14. Subjects who are related to or dependent on the Investigator, Sponsor, or study site such that a conflict of interest could arise.

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT04314544
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 3
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Sun Pharma Global FZE
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

N/A
Principal Investigator Affiliation N/A
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Industry
Overall Status Recruiting
Countries Australia, Spain, United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Active Psoriatic Arthritis
Arms & Interventions

Arms

Experimental: Arm A

Placebo Comparator: Arm B

Interventions

Drug: - TILD

one 1 mL injection of study medication

Drug: - matching placebo injections

one 1 mL injection of placebo

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Sunpharma site no. 17, Fountain Valley, California

Status

Active, not recruiting

Address

Sunpharma site no. 17

Fountain Valley, California, 92708

Sunpharma site no. 15, Thousand Oaks, California

Status

Active, not recruiting

Address

Sunpharma site no. 15

Thousand Oaks, California, 91320

Sunpharma site no. 21, Clearwater, Florida

Status

Active, not recruiting

Address

Sunpharma site no. 21

Clearwater, Florida, 33765

Sunpharma site no. 02, Hialeah, Florida

Status

Recruiting

Address

Sunpharma site no. 02

Hialeah, Florida, 33016

Site Contact

Carlos A Sesin, M.D.

[email protected]

305-456-9062

Sunpharma site no. 19, Miami, Florida

Status

Active, not recruiting

Address

Sunpharma site no. 19

Miami, Florida, 33135

Sunpharma site no. 05, New Port Richey, Florida

Status

Recruiting

Address

Sunpharma site no. 05

New Port Richey, Florida, 34668

Site Contact

Farrukh Zaidi, M.D.

[email protected]

727-849-4131

SunPharma Site no 22, Tamarac, Florida

Status

Active, not recruiting

Address

SunPharma Site no 22

Tamarac, Florida, 33321

Sunpharma site no. 20, Wichita, Kansas

Status

Active, not recruiting

Address

Sunpharma site no. 20

Wichita, Kansas, 67207

Sunpharma Site no 26, Lake Charles, Louisiana

Status

Not yet recruiting

Address

Sunpharma Site no 26

Lake Charles, Louisiana, 70605

Site Contact

Enrique Mendez, M.D.

[email protected]

337-312-8619

Sunpharma site no. 07, Worcester, Massachusetts

Status

Recruiting

Address

Sunpharma site no. 07

Worcester, Massachusetts, 01605

Site Contact

Charles A Birbara, M.D.

[email protected]

508-755-0201

Sunpharma site no. 10, Lansing, Michigan

Status

Active, not recruiting

Address

Sunpharma site no. 10

Lansing, Michigan, 48910

Sunpharma site no. 14, Springfield, Missouri

Status

Active, not recruiting

Address

Sunpharma site no. 14

Springfield, Missouri, 65810

Sunpharma Site no 27, Lincoln, Nebraska

Status

Not yet recruiting

Address

Sunpharma Site no 27

Lincoln, Nebraska, 68516

Site Contact

Melvin Churchill, M.D.

[email protected]

402-420-3433

Sunpharma site no. 09, Rochester, New York

Status

Active, not recruiting

Address

Sunpharma site no. 09

Rochester, New York, 14623

Sunpharma site no. 18, Cincinnati, Ohio

Status

Active, not recruiting

Address

Sunpharma site no. 18

Cincinnati, Ohio, 45242

Sunpharma site no. 11, Middleburg Heights, Ohio

Status

Active, not recruiting

Address

Sunpharma site no. 11

Middleburg Heights, Ohio, 44130

Sunpharma site no. 25, Wyomissing, Pennsylvania

Status

Not yet recruiting

Address

Sunpharma site no. 25

Wyomissing, Pennsylvania, 19610

Site Contact

Michael Borofsky, M.D.

[email protected]

610-375-2466

Sunpharma site no. 13, Baytown, Texas

Status

Active, not recruiting

Address

Sunpharma site no. 13

Baytown, Texas, 77521

Sunpharma site no. 06, Houston, Texas

Status

Active, not recruiting

Address

Sunpharma site no. 06

Houston, Texas, 77004

Sunpharma site no. 08, Houston, Texas

Status

Recruiting

Address

Sunpharma site no. 08

Houston, Texas, 77521

Site Contact

Amber Khan, M.D.

[email protected]

832-672-7973

Sunpharma site no. 04, League City, Texas

Status

Active, not recruiting

Address

Sunpharma site no. 04

League City, Texas, 77573

Sunpharma Site no 28, Lubbock, Texas

Status

Not yet recruiting

Address

Sunpharma Site no 28

Lubbock, Texas, 79410

Site Contact

Jitendra Vasandani, M.D.

[email protected]

806-993-1040

Sunpharma site no. 03, San Antonio, Texas

Status

Recruiting

Address

Sunpharma site no. 03

San Antonio, Texas, 78229

Site Contact

Alex De Jesus, M.D., P.A.

[email protected]

210-980-1742

Sunpharma site no. 16, San Antonio, Texas

Status

Recruiting

Address

Sunpharma site no. 16

San Antonio, Texas, 78229

Site Contact

Pendleton B Wickersham, M.D.

[email protected]

210-477-2626

Sunpharma site no. 01, Tomball, Texas

Status

Recruiting

Address

Sunpharma site no. 01

Tomball, Texas, 77375

Site Contact

Shaikh Arif Ali, M.D.

[email protected]

281-517-0550

Sunpharma site no. 12, Spokane, Washington

Status

Active, not recruiting

Address

Sunpharma site no. 12

Spokane, Washington, 99204

International Sites

Sunpharma site no. 24, Hobart, Tasmania, Australia

Status

Not yet recruiting

Address

Sunpharma site no. 24

Hobart, Tasmania, 7000

Site Contact

Jane Zochling, Mmed, FRACP

[email protected]

61-36223-8802

SunPharma Site No 23, Córdoba, Spain

Status

Not yet recruiting

Address

SunPharma Site No 23

Córdoba, , 14004

Site Contact

Alejandro Escudero Contreras, Degree in Med.

[email protected]

34957010429

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