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Active clinical trials for "Psoriasis"

Results 1101-1110 of 1714

Study of Secukinumab With 2 mL Pre-filled Syringes

Psoriasis

The aim of the study was to demonstrate efficacy, safety and tolerability of 2 mL pre-filled syringe of 300 mg secukinumab in treatment of moderate to severe plaque psoriasis.

Completed20 enrollment criteria

Study to Evaluate the Efficacy of Etanercept Treatment in Adults Who Failed Therapy With Apremilast...

Plaque Psoriasis

To evaluate the efficacy of etanercept in adults with moderate to severe plaque psoriasis who have failed therapy with apremilast (Otezla).

Completed25 enrollment criteria

TAB08 in Patients With Psoriasis Vulgaris, Not Adequately Controlled With Current Treatment

Psoriasis Vulgaris

Study to assess Pharmacodynamics, Safety, Pharmacokinetics and clinical effects of TAB08 during 12 weeks of treatment in patients with Psoriasis Vulgaris, not adequately controlled with current therapy.

Completed8 enrollment criteria

Study of Efficacy and Safety of Secukinumab in Subjects With Moderate to Severe Chronic Plaque-type...

Plaque Psoriasis

The purpose of this study was to determine if secukinumab is effective and safe in the treatment of plaque type psoriasis

Completed17 enrollment criteria

Oral Psoriasis Treatment Adherence and Intervention Study

Psoriasis

Response to psoriasis treatment is variable in large part because of poor adherence treatments. Studies using electronic monitors have assessed adherence to topical and injectable psoriasis treatments and to biologics, yielding critically important insights. Adherence to oral psoriasis treatments is not as well characterized but is also critical, as the therapeutic windows for these treatments are narrower than for other psoriasis treatment options. The proposed study will assess patients' adherence to oral psoriasis treatment (primarily methotrexate) and will also collect pilot data on an intervention to improve adherence. The primary hypothesis of the investigators study is that adherence to oral psoriasis treatment is poor and that a reporting intervention may improve adherence to oral psoriasis treatment. In the investigator-blinded, 6-month prospective study, patients will be randomized to standard-of-care treatment or standard-of-care supplemented with the weekly online reporting intervention. Adherence will be assessed using electronic monitors. This randomized trial will permit the investigators to determine adherence to oral psoriasis treatment, assess the relationship between adherence and psoriasis outcomes, identify factors that are associated with adherence to oral psoriasis treatment (including physician trust, confidence in the treatment plan, and depression), and obtain preliminary data on the impact of an Internet-reporting measure on patients' adherence to oral psoriasis treatment .

Completed8 enrollment criteria

Efficacy, Safety and Immunogenicity of BI 695501 Versus Humira® in Patients With Moderate to Severe...

Psoriasis

To evaluate the efficacy and to compare efficacy and safety of BI 695501 versus Humira in patients with moderate to severe chronic plaque psoriasis.

Completed31 enrollment criteria

Efficacy of Secukinumab Compared to Ustekinumab in Patients With Plaque-type Psoriasis

Chronic Plaque Type Psoriasis

This study assessed efficacy of secukinumab, compared to ustekinumab, in patients that have plaque-type psoriasis

Completed5 enrollment criteria

Efficacy, Tolerability and Safety of LAS41004 Formulations in a Psoriasis Plaque Test

Psoriasis

Clinical investigation of anti-psoriatic efficacy and atrophy

Completed20 enrollment criteria

A Multiple Dose Escalation Study of ASKP1240 in Subjects With Moderate to Severe Plaque Psoriasis...

Psoriasis

The purpose of this study is to explore the safety and tolerability of multiple doses of ASKP1240 compared to placebo and determine Pharmacokinetics and Pharmacodynamics in subjects with moderate to severe psoriasis.

Completed40 enrollment criteria

LEO 90100 Compared With Calcipotriol Plus Betamethasone Dipropionate Ointment, LEO 90100 Vehicle...

Psoriasis Vulgaris

The purpose of this study is to investigate whether LEO 90100 and calcipotriol plus betamethasone are effective in the treatment of psoriasis vulgaris.

Completed28 enrollment criteria
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