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  • A Study in Patients With Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001

    Phase

    3

    Span

    97 weeks

    Sponsor

    Alumis Inc

    Buxtehude, Lower Saxony

    Recruiting

  • A Study to Evaluate the Efficacy and Safety of Subcutaneous Sonelokimab Compared with Placebo in Adult Participants with Moderate to Severe Hidradenitis Suppurativa

    Phase

    3

    Span

    109 weeks

    Sponsor

    MoonLake Immunotherapeutics AG

    Buxtehude

    Recruiting

  • A Trial to Evaluate the Efficacy and Safety of Tralokinumab in Combination With Topical Corticosteroids in Children and Infants With Moderate-to-severe Atopic Dermatitis

    Phase

    3

    Span

    203 weeks

    Sponsor

    LEO Pharma

    Buxtehude

    Recruiting

  • Dose Escalation Trial of Safety, Pharmacokinetic/Pharmacodynamic and Preliminary Clinical Activity of Briquilimab in Adult Patients with Chronic Spontaneous Urticaria (CSU)

    Phase

    1/2

    Span

    122 weeks

    Sponsor

    Jasper Therapeutics, Inc.

    Buxtehude

    Recruiting

  • Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of secukinumAb in Adult Patients With Moderate to Severe Hidradenitis Suppurativa.

    The study will collect data from patients during routine secukinumab treatment and will be representative of the real-world patient population eligible for secukinumab treatment in Germany. In order to attain widespread representation of health care practices related to the use of secukinumab in the approved indication of moderate to severe HS, a broad spectrum of dermatology practices and clinics who are treating patients with HS across Germany will be included.

    Phase

    N/A

    Span

    176 weeks

    Sponsor

    Novartis Pharmaceuticals

    Buxtehude

    Recruiting

  • Binimetinib Plus Encorafenib Real Life Investigation of Next Generation Melanoma Treatment

    Phase

    N/A

    Span

    415 weeks

    Sponsor

    Pierre Fabre Pharma GmbH

    Buxtehude

    Recruiting

  • Clinical Study of Fianlimab in Combination With Cemiplimab Versus Pembrolizumab in Adolescent and Adult Patients With Previously Untreated Unresectable Locally Advanced or Metastatic Melanoma

    Phase

    3

    Span

    468 weeks

    Sponsor

    Regeneron Pharmaceuticals

    Buxtehude

    Recruiting

  • Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib

    Phase

    3

    Span

    157 weeks

    Sponsor

    Incyte Corporation

    Buxtehude

    Recruiting

  • Real-world Effectiveness Study of Long-term Treatment With Dupilumab in Participants ≥6 Years With Atopic Dermatitis

    Phase

    N/A

    Span

    262 weeks

    Sponsor

    Sanofi

    Buxtehude

    Recruiting

  • Safety and Efficacy of EIK1001-006 in Combo With Pembro Versus Placebo and Pembro as First-Line Therapy in Patients With Advanced Melanoma.

    This is a Multicenter, Randomized, Double-Blind, Active Comparator-Controlled, Adaptive Phase 2/3 Study to Evaluate the Safety and Efficacy of EIK1001 and Pembrolizumab Versus Placebo and Pembrolizumab as First-Line Therapy in Participants with Advanced Melanoma. The study includes dose optimization and expansion parts.

    Phase

    2/3

    Span

    815 weeks

    Sponsor

    Eikon Therapeutics

    Buxtehude, Lower Saxony

    Recruiting

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