Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

PD-1 (Programmed Death-1) Versus PD-L1 (Programmed Death-ligand 1) Immune Check Point Inhibitors Combined With Chemotherapy, With or Without Bevacizumab, In Patients With Metastatic, Persistent Or Recurrent Cervical Cancer

This is a randomized trial evaluating the results of using of PD-1 and PD-L1 immune checkpoint inhibitors combined with chemotherapy, with or without bevacizumab, in patients with metastatic, persistent, and recurrent cervical cancer.

Participants needed: 120
Trial details
Phase: Phase 2, Phase 3Age: 18-75Biological sex: FemaleType: InterventionalSponsor: N.N. Alexandrov National Cancer CentreUpdated: May 28, 2026Locations: 1
Eligibility criteria

Age ≥18-≤75 years. [+8]

Presence of another active malignant invasive neoplasm. [+1]

Status: Recruiting

Real World Practice With Academic Anti CD19 CAR-T Cell Therapy in Relapse/Refractory B-cell Lymphoma

Chimeric antigen receptor (CAR) T-cell therapy has been the standard of care for relapsed/refractory large B-cell lymphomas (R/R LBCLs) since 2018. However, high cost of commercial products limits their application in real-world clinical practice. Academic approach to manufacturing CAR-T cell products can reduce the costs and improve availability and affordability of this therapy option. The aim of the present study is assess the efficacy and safety of the use of academic CAR-T cell products in r/r LBCL patients.This prospective observational study with r/r LBCL patients treated in the NN Alexandrov National Cancer Centre of Belarus. The CAR-T cell product was manufactured using lentiviral vector encoding anti-CD19 CAR.

Participants needed: 76
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: N.N. Alexandrov National Cancer CentreUpdated: Apr 13, 2026Locations: 1Duration: 3 Months
Eligibility criteria

age ≥18 years, [+3]

pregnancy, [+2]

Status: Recruiting

PARP (Poly (ADP-ribose) Polymerase) Inhibitor With or Without Angiogenesis Inhibitor in Homologous Recombination Deficient Primary Ovarian Cancer, Fallopian-Tube Cancer, or Primary Peritoneal Cancer

This is a randomized trial evaluating the results of using of PARP inhibitor combined with angiogenesis inhibitor. in patients with homologous recombination deficient primary ovarian cancer, fallopian-tube cancer, or primary peritoneal cancer of the III-IV stages.

Participants needed: 120
Trial details
Phase: Phase 2, Phase 3Age: 18-75Biological sex: FemaleType: InterventionalSponsor: N.N. Alexandrov National Cancer CentreUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Age ≥18-≤75 years. [+6]

Presence of another active malignant invasive neoplasm. [+2]

Status: Recruiting

Limited Versus Extended Lymph Node Dissection During Radical Prostatectomy in Patients With Localized or Locally Advanced Prostate Cancer

This is a randomized controlled study assessing outcome of low (no or limited) versus high (limited or extended) extent of lymph node dissection in addition to radical prostatectomy in patients with operable localized or locally advanced prostate cancer.

Participants needed: 800
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: N.N. Alexandrov National Cancer CentreUpdated: Dec 30, 2025Locations: 1
Eligibility criteria

Age over 18 years. [+5]

Presence of another active malignant invasive neoplasm. [+3]