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Provita Sp. z o.o.

Verified siteinfo

Poland Ul. Fabryczna 13d, 40-611 Katowice, Poland

  • 20 trials recruiting
  • Dermatitis atopic · Psoriasis · Alopecia areata
  • Adults and children

About Specializations

Provita Sp. z o.o. in Katowice, Poland specialises in clinical trials of conditions such as Dermatitis atopic, Psoriasis, Alopecia areata, Hidradenitis, and other specialisations. This site conducts important research.

Main research areas of the site

Immune System Diseases Research

The Dermatology Department at Provita Sp. z o.o. is focused on immune‑mediated conditions such as Alopecia Areata, Allergic Rhinitis/Rhinoconjunctivitis triggered by house dust mite, and Hidradenitis Suppurativa. Current studies aim to evaluate new therapies that can reduce disease activity and improve patient quality of life.

  • Assessing oral JAK inhibitor upadacitinib for severe alopecia areata
  • Evaluating subcutaneous immunotherapy for dust‑mite induced allergic rhinitis
  • Testing biologic agent izokibep in hidradenitis suppurativa

Provita Sp. z o.o., located in Katowice, Poland, is conducting five clinical trials with a team of seven investigators, all within the immune‑system disease therapeutic area.

Skin and Connective Tissue Diseases Research

In the field of Skin and Connective Tissue Diseases, the department investigates disorders that affect the skin’s appearance and function, including Plaque Psoriasis, Hidradenitis Suppurativa, and Alopecia Areata. The primary goal of these trials is to test innovative treatments that target inflammation and promote skin healing.

  • Investigating DC‑806 for moderate to severe plaque psoriasis
  • Studying izokibep in patients with hidradenitis suppurativa
  • Exploring upadacitinib’s impact on skin manifestations of alopecia areata

The Dermatology Department at Provita Sp. z o.o. currently manages five clinical studies, employing seven investigators to advance therapeutic options for skin and connective tissue diseases.

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Site location
Ul. Fabryczna 13d40-611 KatowicePoland
Recruiting now
20 trials
Conditions studied
24
Partner status
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Ongoing trials

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78 clinical trials

Evaluation of Anifrolumab Subcutaneous Treatment in Immunosuppressant‑Naïve and Biologic‑Naïve Patients with Systemic Lupus Erythematosus

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Anifrolumab
  • Sponsor:AstraZeneca AB

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.

Psoriasis

Recruiting

Long-term safety study of deucravacitinib compared to ustekinumab in adults with moderate to severe plaque psoriasis

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Deucravacitinib
  • Sponsor:Bristol-Myers Squibb Services Unlimited Company

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.

Study on Lebrikizumab for Adults with Chronic Rhinosinusitis and Nasal Polyps Using Intranasal Corticosteroids

Registered drug
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Lebrikizumab
  • Sponsor:Eli Lilly & Co.

Oral herpes

Recruiting

Study comparing aciclovir gel and cream effectiveness in treating recurrent cold sores (herpes labialis)

Registered drug
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Aciclovir
  • Sponsor:Laboratorios Ojer Pharma S.L.

Vitiligo

Recruiting

Safety and efficacy of oral ACT-777991 in adults with non‑segmental vitiligo: a randomized, double‑blind, placebo‑controlled Phase 2a trial

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Sponsor:Idorsia Pharmaceuticals Ltd.

Study of Camoteskimab and Sodium Chloride Placebo in Adults with Moderate-to-Severe Atopic Dermatitis

Registered drug
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Sodium Chloride

Nipocalimab in Adults with Moderate to Severe Systemic Lupus Erythematosus

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Nipocalimab
  • Sponsor:Janssen Cilag International

Phase 2b Randomized Double‑Blind Study of Oral PF‑08049820 in Adults with Moderate to Severe Atopic Dermatitis

Investigational
Countries:PolandPoland
  • Participants:18–64 years
  • Sponsor:Pfizer Inc.

A study to evaluate the efficacy and safety of lesigercept in adults with chronic spontaneous urticaria who do not have enough relief from antihistamines

Investigational
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Sponsor:Yuhan Corp.

A study comparing furazidin and clindamycin for women with bacterial vaginosis

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years
  • Substances:Clindamycin Phosphate
  • Sponsor:Adamed Pharma S.A.
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