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Synexus Polska Sp. z o.o.

Poland Ul. Konckiego 3, 40-040 Katowice, Poland

  • 1 trial recruiting
  • Type 2 diabetes mellitus · Gastrooesophageal reflux disease · Erosive oesophagitis
  • Adult patients

About Specializations

Synexus Polska Sp. z o.o. in Katowice, Poland specialises in clinical trials of conditions such as Type 2 diabetes mellitus, Gastrooesophageal reflux disease, Erosive oesophagitis, Obesity, and other specialisations. This site conducts important research.

Main research areas of the site

Digestive System Diseases

At Synexus Polska the focus is on improving outcomes for patients with erosive esophagitis caused by gastroesophageal reflux disease, evaluating newer acid‑suppression agents to sustain healing after initial treatment.

  • Healing of erosive esophagitis
  • Maintenance therapy comparison
  • Long‑term safety monitoring
  • Patient‑reported symptom relief

The trials aim to confirm that the investigational drug can maintain mucosal healing more effectively than standard therapy, offering patients a reliable option for long‑term disease control.

Immune System Diseases

Research at the Katowice site includes studies on moderate‑to‑severe plaque psoriasis, where novel immune‑modulating agents are compared for cardiovascular safety and overall efficacy.

  • Long‑term safety of targeted therapies
  • Cardiovascular outcome assessment
  • Comparative effectiveness of biologics
  • Impact on quality of life

These investigations seek to ensure that emerging treatments not only clear skin lesions but also do not increase heart‑related risks for patients.

Nutritional and Metabolic Diseases

The centre conducts trials on non‑alcoholic steatohepatitis and its broader category metabolic dysfunction‑associated steatohepatitis, as well as on obesity, to test therapies that may halt liver fibrosis and improve metabolic health.

  • Fibrosis regression in compensated cirrhosis
  • Event‑free survival metrics
  • Weight reduction outcomes
  • Liver function improvement

The goal is to determine whether new agents can safely reduce liver damage and support healthier body weight, addressing two major contributors to chronic disease.

Respiratory Tract Diseases

Studies targeting respiratory syncytial virus infections evaluate the immune response generated by a revaccination schedule of the RSVPreF3 OA vaccine in adults over 60 years old.

  • Humoral immunity after revaccination
  • Seasonal timing of dose administration
  • Safety profile in older participants
  • Potential reduction in RSV‑related illness

By measuring antibody levels and monitoring adverse events, the research aims to confirm that the vaccine provides robust protection for the elderly during peak RSV seasons.

Virus Diseases

In addition to respiratory studies, the site explores broader virus diseases strategies, focusing on vaccine effectiveness and immune monitoring to curb viral spread in vulnerable populations.

  • Evaluation of vaccine immunogenicity
  • Development of antiviral prophylaxis
  • Assessment of public health impact
  • Safety surveillance across age groups

The overarching aim is to advance preventive measures that reduce infection rates and improve community health outcomes.

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Site location
Ul. Konckiego 340-040 KatowicePoland
Recruiting now
1 trial
Conditions studied
6

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4 clinical trials

Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Lansoprazole
  • Sponsor:Cinclus Pharma Holding AB (publ)
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:BI 456906
  • Sponsor:Boehringer Ingelheim Espana S.A.
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Duvakitug
  • Sponsor:Teva Branded Pharmaceutical Products R&D LLC
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Legal notice · Published by CTIN POLAND sp. z o.o., ul. rtm. Witolda Pileckiego 67/109, 02-781 Warsaw, Poland · KRS 0001111334 · REGON 528919042 · NIP 9512598637

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On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).