Clinical trials

7

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

Condition / disease
Location
Status: Recruiting

Refusal of Sentinel Lymph Node Biopsy in Patients With Luminal A Subtype Early Breast Cancer

Sentinel lymph node biopsy (SLNB) is the standard of axillary lymph node surgical staging in patients with early breast cancer. The main goal of the study is to abandon axillary surgery in patients over 59 years old with early, luminal A, clinical lymph node negative breast cancer.

Participants needed: 100
Trial details
Age: 60+Biological sex: FemaleType: InterventionalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: May 12, 2026Locations: 1
Eligibility criteria

HER2-negative breast cancer (ER +/ PR +), Ki67 <= 30%, G1-2 [+7]

Inconsistency with inclusion criteria. [+4]

Status: Recruiting

High-dose Chemotherapy as Second-line Drug Therapy for Relapsed Germ Cell Tumors

This is a prospective, single-center, non-randomized phase II study. Patients with germ cell tumors of gonadal and extragonadal localization who have progressed after prior platinum-containing first-line chemotherapy will receive high-dose chemotherapy with TI (2 cycles) folollowed by high dose CE chemotherapy with autologous stem cell transplantation (3 cycles). The primary endpoint of the study is to evaluate the efficacy high-dose chemotherapy as second-line drug therapy for patients with advanced germ cell tumors.

Participants needed: 25
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: Aug 3, 2025Locations: 1
Eligibility criteria

Patient is able to provide informed consent and sign approved consent forms to p... [+9]

Primary CS of the brain [+3]

Status: Recruiting

Chemo-immunotherapy in Patients Under 18 Years of Age With Bone and Soft Tissue Sarcomas

Data from 40 patients are planned to be included in the study to randomize approximately 10 patients. This study involves patients with advanced/metastatic GD2-positive rhabdomyosarcoma after progression on 1st line of chemotherapy, advanced/metastatic GD2-positive Ewing sarcoma after progression on 1st line of chemotherapy and advanced/metastatic GD2-positive osteosarcoma after progression on 1st line of chemotherapy. All patients will receive therapy until disease progression (a total of 6 courses of immunotherapy). The primary objective of the study is to determine the efficacy and safety of dinutuximab beta with investigator's choice of chemotherapy.

Participants needed: 40
Trial details
Phase: Phase 3Age: Up to 18Biological sex: AllType: InterventionalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: Nov 1, 2024Locations: 1
Eligibility criteria

Signed written informed consent form; [+8]

Withdrawal of consent by the patient or his/her parent/guardian. [+1]

Status: Recruiting

Biobank and Register of Patients With Agresive Tumors for Translational and Analytical Research

The investigators will collect biosamples of patient blood and tumour tissue for further immunological analysis of blood cell subpopulations, immunosupressive factors concentration, HLA expression an lymphocytes and tumour tissue, and and cancer testis antigenes expression on tumour cells, as well as clinical data on patient's stage, therapy, response and demographics. Possible prognostic and predictive dynamic biomarkers will be discovered for individualisation of treatment strategies

Participants needed: 1,000
Trial details
Age: 1+Biological sex: AllType: ObservationalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: May 6, 2024Locations: 1Duration: 5 Years
Eligibility criteria

Signed inform consent [+4]

Concurrent Lymphoprolipherative disorder [+5]

Status: Recruiting

Leflunomide or Combination of MEK Inhibitor and Hydroxychloroquine for Refractory Patients With RAS Mutations

There is a huge variety of nucleotide substitutions that activate RAS. The search for new "universal" drugs for the RAS pathway that either interfere with RAS upregulation upstream in the signaling pathway or offset the consequences of RAS activation is important for improving therapeutic outcomes for patients with refractory malignancies. The use of leflunomide or the combination of MEK inhibitor + hydroxychloroquine ± bevacizumab is promising for patients with mutations in RAS cascade genes who have failed all existing treatment standards.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-85Biological sex: AllType: InterventionalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: Jan 29, 2024Locations: 1
Eligibility criteria

Patient is able to provide informed consent and sign approved consent forms to p... [+14]

Age over 85 years. [+11]

Status: Recruiting

Refusal of Breast Surgery in Patients With Breast Cancer With a Clinical Complete Response (cCR) After Neoadjuvant Systemic Therapy and a Confirmed Pathological Complete Response (pCR) Using Vacuum-assisted Biopsy (VAB) and Sentinel Lymph Node Biopsy (SLNB)

The main goal of the study is to abandon breast surgery in patients with breast cancer with a clinical complete response (cCR) after neoadjuvant systemic therapy and confirmed pCR using Vacuum-assisted biopsy (VAB) and sentinel lymph node biopsy (SLNB). Evidence of the high diagnostic accuracy (sensitivity and specificity) of vacuum aspiration biopsy in determining pCR in patients with clinical complete response after neoadjuvant systemic therapy will allow abandoning breast surgery in favor of radiation therapy alone, improving the quality of life of these patients.

Participants needed: 60
Trial details
Age: 18-70Biological sex: FemaleType: InterventionalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: Jun 15, 2022Locations: 1
Eligibility criteria

age> 18 years. [+6]

Inconsistency with inclusion criteria. [+7]

Status: Recruiting

Combined Treatment of Patients With Soft Tissue Sarcoma Including Preoperative Stereotactic Radiation Therapy and Postoperative Conformal Radiation Therapy

Combined treatment of soft tissue sarcoma includes 3 steps: 1. step - preoperative stereotactic radiation therapy in hypofractionation mode 2. step - operation 3. step - postoperative conformal radiation therapy in normofractionation mode

Participants needed: 30
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: N.N. Petrov National Medical Research Center of OncologyUpdated: Apr 1, 2020Locations: 1
Eligibility criteria

morphologically verified diagnosis of soft tissue sarcoma [+5]

previous radiation treatment [+6]