A Study to Evaluate the Effectiveness of STELARA ™ (USTEKINUMAB) in the Treatment of Scalp Psoriasis

Status unconfirmed · Phase 4 · Has a placebo group

Conditions studied: Scalp Psoriasis, Plaque Psoriasis

In brief

This is a single site, randomized, placebo-controlled, cross-over trial of sub-cutaneous injections of placebo and Stelara™ (ustekinumab) in subjects with scalp psoriasis.The purpose of the study is to assess the effectiveness of Stelara™ (ustekinumab)in the treatment of scalp psoriasis by determining the proportion of subjects who clear or almost clear in scalp specific physician assessments. The study will include approximately 30 subjects.

Key facts

Study ID

NCT01558310

Run by

Paul Steven Yamauchi, MD, PhD

People needed

30

Starts

2012-08-01

Expected to finish

2013-12-01

Last updated by the study team

2012-07-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Capable of giving informed consent and the consent must be obtained prior to any study related procedures.
• Be 18 years of age or older at the time of consent; may be male or female.
• Have had a diagnosis of plaque psoriasis at least 6 months prior to administration of study agent.
• Presence of moderate or severe psoriasis on the body other than the scalp.
• At least 30% of scalp affected with erythema, induration and desquamation and s-PGA score greater than or equal to 4.
• Be candidates for phototherapy or systemic treatment of psoriasis.
• Women of childbearing potential and all men must be using adequate birth control measures (eg abstinence, oral contraceptives, intrauterine device, barrier method with spermicide, or surgical sterilization) and must agree to continue use of such measures and not become pregnant or plan a pregnancy until 12 months after receiving the last injection of study agent.
• Be able to adhere to protocol requirements and study visit schedule.
• Must agree not to receive a live virus or live bacterial vaccination during the trial and 12 months after last study injection.
• Must agree not to receive a BCG vaccination during the trial and up to 12 months after the last injection.
• Must avoid prolonged sun exposure and avoid use of tanning booths or other ultraviolet light sources during the study.
• Are considered eligible according to the following tuberculosis (TB) screening criteria:
• Have no history of latent or active TB prior to screening. An exception is made for subjects currently receiving treatment for latent TB with no evidence of active TB, or who have a history of latent TB and documentation of having completed appropriate treatment for latent TB within 3 years prior to the first administration of study agent. It is the responsibility of the investigator to verify the adequacy of previous antituberculous treatment and provide appropriate documentation.
• Have no signs or symptoms suggestive of active TB upon medical history and/or physical examination.
• Within 6 weeks prior to the first administration of study agent, have a negative QuantiFERON-TB Gold test result (see Attachment #).Indeterminate results should be handled as outlined in Section #, Exclusion Criteria.
• Have a chest radiograph (both posterior-anterior and lateral views), taken within 3 months prior to the first administration of study agent and read by a qualified radiologist, with no evidence of current, active TB or old, inactive TB.
• Have screening laboratory test results within the following parameters:
• Hemoglobin > 10g/dL
• White Blood Cells > 3.5 x 109 /L
• Neutrophils > 1.5 x 109 /L
• Platelets > 100 X109 /L
• Serum Creatinine < 1.5 mg/dL ( or 133 micromol/L )
• AST,ALT, and alkaline phosphatase levels must be within 1.5 times the upper limit of normal range for the laboratory conducting the test

You may not qualify if…

• Subjects meeting any of the following criteria may not be enrolled in the study:
• Currently have non-plaque forms of psoriasis (erythrodermic, guttate, or pustular).
• Have current drug-induced psoriasis.
• Presence of any skin conditions ( including scalp) other than psoriasis that would interfere with evaluations of the effect of study agents.
• Are pregnant, nursing, or planning pregnancy (both men and women) while enrolled in the study.
• Have used any therapeutic agent targeted at reducing IL-12 and/or IL-23, including but not limited to ustekinumab and ABT -874.
• Have used any investigational drug within the previous 4 weeks or 5 times the half-life of the investigational agent, whatever is longer.
• Have used any investigational drug within the previous 3 months or 5 times the half-life of the biological, whichever is longer.
• Have ever received natalizumab or other agents that target alpha-4-integrin.
• Have received phototherapy or any any systemic medications/treatments that could affect psoriasis or s-PGA/PASI evaluations ( including but not limited to, oral or injectable corticosteroids, retinoids,1,25 dihydroxy vitamin D3 and analogues, psoralens, sulfasalazine, hydroxyurea, or fumaric acid derivatives) within 4 weeks of administration of study agent.
• Have used topical mediations/treatments that could affect psoriasis or s-PGA/PASI evaluation ( eg corticosteroids , anthralin, calcipotriene, topical vitamin D derivatives, retinoids, tazarotene, methoxsalen,trimethylpsoralens) within 2 weeks of the first administration of study agent.
• Have used any systemic immunosuppressants ( eg Methotrexate, azathioprine, cyclosporine,6-thioguanine, mercaptopurine, mycophenolate, mofetil, hydroxyurea, and tacrolimus) within 4 weeks of the first administration of study agent.
• Are currently receiving lithium, anti-malarials, or intramuscular gold, or have received lithium, anti-malarials, or intramuscular gold, or have received lithium, anti-malarials, or intramuscular gold within 4 weeks of the first administration of study agent.
• Have received within 3 months prior to the first injection a live virus or bacterial vaccination. Subjects must agree not to receive a live virus or bacterial vaccination during the trial or up to 12 month after the last study agent injection.
• Have had a BCG vaccination within 12 months of screening. Subject must agree not to receive a BCG vaccination during the trial or up to 12 months after the last study agent injection.
• Have a history of chronic or recurrent infectious disease, including but not limited to chronic renal infection, chronic chest infections (eg bronchiectasis), recurrent urinary tract infections (recurrent pyelonephritis or chronic non-remitting cystitis), or open, draining, or infected skin wounds or ulcers.
• Have or have had a serious infection (eg sepsis, pneumonia,or pyelonephritis) or have been hospitalized or received IV antibiotics for an infection during the 2 months prior to screening
• Have a history of latent or active granulomatous infection, including histoplasmosis or coccidioidomycosis, prior to screening.
• Have persistently indeterminate (indeterminate on repeat sampling) QuantiFERON-TB Gold test results
• Have had a Bacille Calmette-Guérin (BCG) vaccination within 12 months of screening.
• Have a chest radiograph within 3 months prior to the first administration of study agent that shows an abnormality suggestive of a malignancy or current active infection, including TB.
• Have had a non-tuberculous mycobacterial infection or opportunistic infection (eg, cytomegalovirus, pneumocystosis, aspergillosis) within 6 months prior to screening.
• Known to be infected with human immunodeficiency virus, hepatitis B, or hepatitis C.
• Have current signs or symptoms of severe, progressive, or uncontrolled renal, hepatic, haematological, gastrointestinal, endocrine, pulmonary, cardiac, neurologic, cerebral, or psychiatric disease.
• Have a transplanted organ.

Where it is running

• Clinical Science Institute — Santa Monica, California, United States

Full record on ClinicalTrials.gov

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