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Recruiting NCT06785818

NCT06785818 Long-term Follow up Local Registry Study of Kymriah in South Korea

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Clinical Trial Summary
NCT ID NCT06785818
Status Recruiting
Phase
Sponsor Novartis Pharmaceuticals
Condition B-Cell Acute Lymphoblastic Leukemia, Diffuse Large B-Cell Lymphoma, Follicular Lymphoma
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2025-03-12
Primary Completion 2039-12-30

Eligibility & Interventions

Sex All sexes
Min Age 0 Years
Max Age 100 Years
Study Type OBSERVATIONAL
Interventions
Tisagenlecleucel

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 500 participants in total. It began in 2025-03-12 with a primary completion date of 2039-12-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is multicenter, primary data collection, non-interventional registry study to assess long-term safety, secondary malignancy risk, and effectiveness of tisagenlecleucel in patients with B-cell malignancies in a routine clinical practice setting in Korea.

Eligibility Criteria

Inclusion Criteria: 1. Patients who receive tisagenlecleucel infusion in the commercial setting, treated under a managed access program or other pathway, e.g., when product was manufactured for the commercial setting but turned out to be out of specification (OOS). 2. Consented to data collection. Exclusion Criteria: 1\. Patients who are enrolled or will be enrolled in the Novartis long term follow-up protocol CCTL019A2205B.

Contact & Investigator

Central Contact

Novartis Pharmaceuticals

✉ novartis.email@novartis.com

📞 +41613241111

Principal Investigator

Novartis Pharmaceuticals

STUDY DIRECTOR

Novartis Pharmaceuticals

Frequently Asked Questions

Who can join the NCT06785818 clinical trial?

This trial is open to participants of all sexes, aged 0 Years or older, up to 100 Years, studying B-Cell Acute Lymphoblastic Leukemia, Diffuse Large B-Cell Lymphoma, Follicular Lymphoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06785818 currently recruiting?

Yes, NCT06785818 is actively recruiting participants. Contact the research team at novartis.email@novartis.com for enrollment information.

Where is the NCT06785818 trial being conducted?

This trial is being conducted at Bundang Gu, South Korea, Seongnam-si, South Korea, Gyeonggi-do, South Korea, Incheon, South Korea and 11 additional locations.

Who is sponsoring the NCT06785818 clinical trial?

NCT06785818 is sponsored by Novartis Pharmaceuticals. The principal investigator is Novartis Pharmaceuticals at Novartis Pharmaceuticals. The trial plans to enroll 500 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology