Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
  • Neoplasms, Connective and Soft Tissue
  • Sarcoma
Type
Interventional
Phase
Phase 1Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Vaccination is carried out on the planned days ± 3 days All examinations must be performed before the vaccine is administered. Full physical examination. Assessment of vital signs (blood pressure, temperature, heart rate), the general condition of the patient and physical activity. Evaluation of con...

Vaccination is carried out on the planned days ± 3 days All examinations must be performed before the vaccine is administered. Full physical examination. Assessment of vital signs (blood pressure, temperature, heart rate), the general condition of the patient and physical activity. Evaluation of concomitant therapy. Assessment of vital signs. Laboratory safety and immunological indicators Assessment of adverse events, symptoms and syndromes of the disease. Introduction of CV in accordance with the dose determined for a given vaccination (see section 9.2. - procedures for delivery and use) After administration, patients are observed for at least 1 hour. An assessment of vital indicators. Undesirable effects detected at the introduction are recorded.

Tracking Information

NCT #
NCT01883518
Collaborators
Not Provided
Investigators
Study Chair: Yuriy Komarov, PhD N. N. Petrov Research Institute of oncology