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Comparison of Immunogenicity of Different Influenza Vaccines in Patients With Hematologic Malignancies

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This randomized controlled trial evaluates and compares the immunogenicity of three different influenza vaccine formulations: high-dose trivalent (HD-IIV3), MF59-adjuvanted quadrivalent (aIIV4), and standard-dose trivalent (SD-IIV3) vaccines. The study population consists of patients with hematologic malignancies, including those undergoing autologous stem cell transplantation or CAR-T cell therapy. The primary goal is to identify which vaccine strategy elicits the most robust antibody and T cell-mediated immune responses in this severely immunocompromised population

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Adults aged 19 years or older

• Confirmed diagnosis of hematologic malignancy, including:

⁃ non-Hodgkin lymphoma, Hodgkin lymphoma, acute leukemia, chronic leukemia, or plasma cell disorders

Locations
Other Locations
Republic of Korea
Asan Medical Center
RECRUITING
Seoul
Contact Information
Primary
So Yun Lim, MD, PhD
soyun_lim@amc.seoul.kr
+82-10-4120-3816
Backup
Sung-Han Kim, MD, PhD
shkimmd@amc.seoul.kr
+82-2-3010-3305
Time Frame
Start Date: 2025-12-04
Estimated Completion Date: 2028-04-30
Participants
Target number of participants: 60
Treatments
Active_comparator: Standard dose Influenza vaccine
Standard dose Influenza vaccine
Experimental: High dose influenza vaccine
High dose influenza vaccine
Experimental: MF.59 adjuvant influenza vaccine
MF.59 adjuvant influenza vaccine
Related Therapeutic Areas
Sponsors
Leads: Asan Medical Center

This content was sourced from clinicaltrials.gov