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Royalderm Agnieszka Nawrocka

Poland ul. Krzysztofa Kieślowskiego 3B/3, 02-962 Warsaw, Poland

  • 1 trial recruiting
  • Chronic spontaneous urticaria · Dermatitis atopic · Psoriasis
  • Adult patients

About Specializations

Royalderm Agnieszka Nawrocka in Warsaw, Poland specialises in clinical trials of conditions such as Chronic spontaneous urticaria, Dermatitis atopic, Psoriasis, and other specialisations. This site conducts important research.

Main research areas of the site

Skin and Connective Tissue Diseases

The research at Royalderm Agnieszka Nawrocka evaluates innovative biologic therapies for inflammatory skin conditions, comparing their effectiveness and safety with existing standards.

  • Plaque psoriasis
  • Moderate to severe atopic dermatitis
  • Chronic spontaneous urticaria

Studies aim to demonstrate therapeutic equivalence, achieve high response rates, and assess long‑term disease control for patients in Warsaw.

Immune System Phenomena

Investigations target the underlying immune mechanisms that drive skin and connective‑tissue disorders, seeking to refine treatment strategies and predict disease progression.

  • Immune system modulation in dermatology
  • Evaluation of treatment durability
  • Biomarker development for response prediction

The work supports the development of next‑generation therapies and enhances understanding of immune‑driven skin disease.

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Site location
ul. Krzysztofa Kieślowskiego 3B/302-962 WarsawPoland
Recruiting now
1 trial
Conditions studied
3

More sites in WarsawPoland

Recruiting now

Ongoing trials

Clinical trials currently enrolling participants at this site.

Condition
Type of trial
Recruitment status
Quick filters

3 clinical trials

Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Barzolvolimab
  • Sponsor:Celldex Therapeutics Inc.

Dermatitis atopic

Not recruiting
Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Ro7790121
  • Sponsor:F. Hoffmann-La Roche AG
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Secukinumab
  • Sponsor:Celltrion Inc.
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