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Centrum Onkologii Ziemi Lubelskiej Im. Sw. Jana Z Dukli

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Poland Ul. Dra Kazimierza Jaczewskiego 7, 20-090 Lublin, Poland

  • 23 trials recruiting
  • Breast cancer · Plasma cell myeloma · Chronic lymphocytic leukaemia
  • Adults and children

About Specializations

Centrum Onkologii Ziemi Lubelskiej Im. Sw. Jana Z Dukli in Lublin, Poland specialises in clinical trials of conditions such as Breast cancer, Plasma cell myeloma, Chronic lymphocytic leukaemia, Endometrial cancer, and other specialisations. This site conducts important research.

Main research areas of the site

Digestive System Diseases

The research team at Centrum Onkologii Ziemi Lubelskiej is conducting a series of studies on cancers of the gastrointestinal tract, aiming to improve survival and quality of life by testing novel targeted agents, immunotherapies, and diagnostic tools.

  • Advanced gastric and gastro‑esophageal junction adenocarcinoma
  • Esophageal squamous cell carcinoma
  • Unresectable hepatocellular carcinoma
  • Metastatic BRCA‑mutated pancreatic cancer
  • Combination regimens with checkpoint inhibitors for digestive cancers

These trials bring together more than thirty investigators to evaluate new treatment options for patients across Lublin and the broader region.

Hemic and Lymphatic Diseases

A robust portfolio of hematology studies focuses on B‑cell malignancies and related disorders, with the goal of establishing more effective and tolerable therapies for both newly diagnosed and relapsed patients.

  • Chronic lymphocytic leukemia / small lymphocytic lymphoma
  • Mantle cell lymphoma and other aggressive B‑cell lymphomas
  • Diffuse large B‑cell lymphoma, including high‑risk subgroups
  • Multiple myeloma, including relapsed/refractory disease
  • Acute myeloid leukemia with NPM1 mutation

Investigators are exploring BTK inhibitors, bispecific antibodies, and CAR‑T cell approaches to deepen responses and reduce disease burden.

Immune System Diseases

Clinical research at the site includes pioneering work on immune‑modulating therapies, ranging from checkpoint blockade to gene‑engineered cellular products, to enhance anti‑tumor immunity and address primary immunodeficiencies.

  • Gene‑modified T‑cell therapy safety and long‑term efficacy
  • PD‑1/PD‑L1 inhibitors such as pembrolizumab and durvalumab
  • Combination immunotherapy with axitinib or tiragolumab
  • Primary immunodeficiency disease diagnostics using advanced imaging
  • Evaluation of novel immune checkpoint combinations in solid tumours

The programme seeks to define optimal regimens that balance potency with safety for patients with complex immune‑related conditions.

Neoplasms

A wide‑ranging oncology portfolio addresses major solid tumours, aiming to compare new targeted agents and combination strategies against standard chemotherapy to improve progression‑free and overall survival.

  • Hormone‑receptor‑positive, HER2‑negative early and advanced breast cancer
  • HER2‑positive metastatic breast cancer and neoadjuvant settings
  • Ovarian cancer, including BRCA‑mutated and platinum‑sensitive disease
  • Prostate cancer with advanced or metastatic disease
  • Metastatic melanoma and head & neck squamous cell carcinoma

Through collaborations with international sponsors, the centre evaluates CDK4/6 inhibitors, antibody‑drug conjugates, and novel hormone therapies to set new standards of care.

Skin and Connective Tissue Diseases

Targeted investigations into cutaneous malignancies and related disorders are underway, focusing on innovative immunotherapies and precision medicines to improve outcomes for patients with skin‑derived cancers.

  • Advanced melanoma, including brain‑metastatic cohorts
  • Cutaneous T‑cell lymphoma and other skin‑related lymphoid neoplasms
  • Evaluation of checkpoint inhibitors in skin cancer subtypes
  • Biomarker‑driven studies for connective‑tissue tumor profiling
  • Safety assessment of combination regimens involving targeted agents

The department leverages its expertise in dermatologic oncology to generate data that may translate into more personalized treatment pathways.

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Site location
Ul. Dra Kazimierza Jaczewskiego 720-090 LublinPoland
Recruiting now
23 trials
Conditions studied
49
Partner status
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Ongoing trials

Clinical trials currently enrolling participants at this site.

Condition
Type of trial
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Quick filters

68 clinical trials

Breast cancer

Recruiting

Study of BNT327 and a drug combination for patients with untreated metastatic or locally recurrent triple-negative breast cancer

Registered drug
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Carboplatin
  • Sponsor:BioNTech SE

Phase 3 Study Comparing JNJ-79635322 with Teclistamab in Patients with Relapsed or Refractory Multiple Myeloma after 1‑3 Prior Treatments

InvestigationalNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Teclistamab
  • Sponsor:Janssen Cilag International

Rinatabart Sesutecan plus bevacizumab vs standard care as maintenance for recurrent platinum‑sensitive ovarian cancer after second‑line chemotherapy

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Bevacizumab
  • Sponsor:Genmab A/S

Study of nivolumab plus drug combination versus standard first-line therapy in patients with advanced Hodgkin lymphoma

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Brentuximab Vedotin

AZD0120 versus standard regimens in patients with relapsed or refractory multiple myeloma

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:AZD0120
  • Sponsor:AstraZeneca AB

A study to investigate the safety and effects of ceralasertib, tremelimumab, and durvalumab in adults with various solid tumors

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

Endometrial cancer+2

Recruiting

A study comparing Rinatabart Sesutecan to other treatments in patients with endometrial cancer who have previously received platinum-based chemotherapy and PD-L1 therapy

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Paclitaxel
  • Sponsor:Genmab A/S

Breast cancer

Recruiting

Study of inavolisib, ribociclib, and fulvestrant for patients with advanced hormone-receptor-positive, HER2-negative breast cancer.

Registered drug
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Fulvestrant
  • Sponsor:F. Hoffmann-La Roche AG

B-cell lymphoma

Recruiting

A study comparing AZD0486 after reduced chemotherapy versus standard chemotherapy in older or unfit patients with newly diagnosed large B-cell lymphoma

Registered drugNo placebo
Countries:PolandPoland
  • Participants:65+ years
  • Substances:Cyclophosphamide
  • Sponsor:AstraZeneca AB

Study of Revumenib and Chemotherapy for Patients with Newly Diagnosed Acute Myeloid Leukemia with NPM1 Gene Mutation

Registered drug
Countries:PolandPoland
  • Participants:0–17 years · 18–64 years · 65+ years
  • Substances:Cytarabine
  • Sponsor:Syndax Pharmaceuticals Inc.

A Study of Amivantamab With Carboplatin and Pembrolizumab for Patients With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Amivantamab
  • Sponsor:Janssen Cilag International

Breast cancer+2

Recruiting

A Study Comparing RLY-2608 and Fulvestrant with Capivasertib and Fulvestrant for Patients with PIK3CA-Mutant Hormone Receptor Positive, HER2-Negative Advanced Breast Cancer

Registered drugNo placebo
Countries:PolandPoland
  • Participants:18–64 years · 65+ years
  • Substances:Capivasertib
  • Sponsor:Relay Therapeutics Inc.
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