Bouzille, France
A Study in Patients With Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001
Phase
3Span
97 weeksSponsor
Alumis IncBuxtehude, 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
3Span
109 weeksSponsor
MoonLake Immunotherapeutics AGBuxtehude
Recruiting
Buxtehude
Recruiting
Dose Escalation Trial of Safety, Pharmacokinetic/Pharmacodynamic and Preliminary Clinical Activity of Briquilimab in Adult Patients with Chronic Spontaneous Urticaria (CSU)
Phase
1/2Span
122 weeksSponsor
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/ASpan
176 weeksSponsor
Novartis PharmaceuticalsBuxtehude
Recruiting
Binimetinib Plus Encorafenib Real Life Investigation of Next Generation Melanoma Treatment
Phase
N/ASpan
415 weeksSponsor
Pierre Fabre Pharma GmbHBuxtehude
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
3Span
468 weeksSponsor
Regeneron PharmaceuticalsBuxtehude
Recruiting
Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib
Phase
3Span
157 weeksSponsor
Incyte CorporationBuxtehude
Recruiting
Real-world Effectiveness Study of Long-term Treatment With Dupilumab in Participants ≥6 Years With Atopic Dermatitis
Phase
N/ASpan
262 weeksSponsor
SanofiBuxtehude
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
2/3Span
815 weeksSponsor
Eikon TherapeuticsBuxtehude, Lower Saxony
Recruiting