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Gyncentrum Sp. z o.o.

Verified siteinfo

Poland Ul. Tadeusza Kosciuszki 229, 40-600 Katowice, Poland

  • 35 trials recruiting
  • Dermatitis atopic · Colitis ulcerative · Chronic spontaneous urticaria
  • Adults and children

About Specializations

Gyncentrum Sp. z o.o. in Katowice, Poland specialises in clinical trials of conditions such as Dermatitis atopic, Colitis ulcerative, Chronic spontaneous urticaria, Neurodermatitis, and other specialisations. This site conducts important research.

Main research areas of the site

Immune System Diseases

The dermatology unit at Gyncentrum Sp. z o.o. is investigating immune‑mediated skin disorders, with a focus on Atopic Dermatitis and the potential of novel biologic agents to improve patient outcomes.

  • Evaluation of rocatinlimab in combination with topical therapies
  • Placebo‑controlled, double‑blind efficacy assessment
  • Use of the Validated Investigator’s Global Assessment to measure disease improvement

With 15 investigators contributing, the site aims to expand therapeutic options for immune‑driven skin conditions while maintaining a patient‑focused approach.

Nervous System Diseases

Research at this clinic also addresses neuropathic itch, specifically moderate‑to‑severe pruritus linked to Notalgia Paresthetica, by testing oral agents that target nerve‑related pathways.

  • Dose‑finding study of difelikefalin versus placebo
  • Measurement of itch intensity reduction after eight weeks of treatment
  • Assessment of safety and tolerability in adult participants

These trials contribute to a better understanding of how nervous system dysfunction drives chronic itching and explore new avenues for relief.

Skin and Connective Tissue Diseases

The department’s broader dermatology program evaluates both disease severity and therapeutic synergy in conditions such as Atopic Dermatitis, integrating systemic and topical approaches.

  • Monitoring disease activity with the Eczema Area and Severity Index (EASI)
  • Combining topical corticosteroids and calcineurin inhibitors with investigational agents
  • Tracking clinical outcomes in moderate‑to‑severe patients

Located in Katowice, Poland, the non‑commercial site leverages its expertise to advance care for skin and connective tissue disorders across Europe.

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Site location
Ul. Tadeusza Kosciuszki 22940-600 KatowicePoland
Recruiting now
35 trials
Conditions studied
53
Partner status
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Ongoing trials

Clinical trials currently enrolling participants at this site.

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Type of trial
Recruitment status
Quick filters

85 clinical trials

Obesity+2

Recruiting

Effect of zenagamtide on major adverse cardiovascular events in overweight or obese adults with established atherosclerotic cardiovascular disease

Investigational
Countries:PolandPoland
  • Participants:18–64 years
  • Substances:POLYPEPTIDE CONSISTING OF A GLUCAGON-LIKE PEPTIDE-1 RECEPTOR AGONIST AND AN AMYLIN RECEPTOR AGONIST, CONNECTED BY A LINKER WITH 4 GLYCINE RESIDUES, AND CONNECTED TO A C18 FATTY ACID SIDE CHAIN
  • Sponsor:Novo Nordisk A/S

Study of LY4268989 adipic acid in adults with moderately to severely active ulcerative colitis

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Sponsor:Eli Lilly & Co.

Long‑Term Safety and Efficacy of SPY001-001, SPY002 and SPY003 in Adults with Ulcerative Colitis

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:SPY002
  • Sponsor:Spyre Therapeutics Inc.

A Phase 3 Study of Efimosfermin Alfa to Assess Safety and Tolerability in Adults with F2‑F3 Stage Metabolic Dysfunction‑Associated Steatohepatitis (MASH)

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Sponsor:Glaxosmithkline Research & Development Limited

Safety and Efficacy of Efimosfermin Alfa in Participants with Biopsy‑Confirmed F2‑ or F3‑Stage Metabolic Dysfunction‑Associated Steatohepatitis (MASH)

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Sponsor:Glaxosmithkline Research & Development Limited

Alopecia areata

Recruiting

A study to evaluate the effectiveness and safety of LAD603 in adults with severe to very severe alopecia areata

Investigational
Countries:PolandPoland
  • Participants:18–64 years
  • Sponsor:Almirall S.A.

Eczema nummular

Recruiting

A study to evaluate the effectiveness and safety of lebrikizumab in adults with nummular eczema who do not respond well to topical corticosteroids.

Registered drug
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Lebrikizumab
  • Sponsor:Almirall S.A.

Asthma

Recruiting

Study to evaluate the long-term safety and effectiveness of lunsekimig in adults with moderate to severe asthma

InvestigationalNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Sponsor:Sanofi-Aventis Recherche & Developpement

COVID-19

Recruiting

A study testing molnupiravir in adults with COVID-19 who are not hospitalized and are at high risk for serious illness

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Molnupiravir
  • Sponsor:Merck Sharp & Dohme LLC

A Study of Long-acting Antibodies SPY001-001 and SPY002 Alone and Combined for Adults with Moderate to Severe Ulcerative Colitis

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:SPY002
  • Sponsor:Spyre Therapeutics Inc.

Vitiligo+2

Recruiting

Long-term safety study of oral povorcitinib in patients with hidradenitis suppurativa, prurigo nodularis, or vitiligo who previously participated in clinical trials

InvestigationalNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Povorcitinib
  • Sponsor:Incyte Corp.

Long-term safety and effectiveness study of APG777 injection in patients with moderate-to-severe atopic dermatitis who previously received APG777 treatment

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:APG777
  • Sponsor:Apogee Therapeutics Inc.
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