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Managed Access Programs for CTL019, Tisagenlecleucel

Managed Access Programs for CTL019, Tisagenlecleucel

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT03601442
Enrollment
Unknown
Registered
2018-07-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Lymphoma, Off-label Indications

Keywords

MAP, Expanded Access, Lymphoma, Leukemia, Off-label indications

Brief summary

The purpose of this registration is to list Managed Access Programs (MAPs) related to CTL019, Tisagenlecleucel

Detailed description

CCTL019B2003I - Available - Managed Access Program (MAP) to provide access to patients with out-of-specification (OOS) leukapheresis product and/or OOS manufactured CTL019 CCTL019B2004I - Available - Managed Access Program (MAP) to provide access to reinfusion for approved indications CCTL019A02001I - Available - Managed Access Program (MAP) to provide access to CLT019 in off-label indications

Interventions

BIOLOGICALCTL019

CTL019

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
0 Days to No maximum
Healthy volunteers
No

Inclusion criteria

An independent request was received from a licensed physician. The patient has a serious or life-threatening disease or condition and there is no comparable or satisfactory alternative therapy available for diagnosis, monitoring, or treatment. The patient is not eligible or able to enrol in a clinical trial or continue participation in such trial. There is a potential patient benefit to justify the potential risk of the treatment use, and the potential risk is not unreasonable in the context of the disease or condition to be treated. The patient must meet any other medical criteria established by the medical experts responsible for the product or by the health authority in the country of request (as applicable). Provision of the product will not interfere with the initiation, conduct, or completion of a Novartis clinical trial or overall development program. Managed Access provision is allowed per local laws/regulations.

Contacts

CONTACTMAP requests are initiated by a licensed physician. https// www.novart is.com/healthcare-professionals/managed-access-programs
novartis.email@novartis.com1-888-669-6682
CONTACTNovartis Pharmaceuticals
+41613241111
STUDY_DIRECTORNovartis Pharmaceuticals

Novartis Pharmaceuticals

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026