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Managed Access Programs for LEE011, Ribociclib

Managed Access Programs for LEE011, Ribociclib

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT05038631
Enrollment
Unknown
Registered
2021-09-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-13

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

Conditions

Breast Cancer

Keywords

MAP, Manage access program, CLEE011, Ribociclib

Brief summary

The purpose of this registration is to list Managed Access Programs (MAPs) related to LEE011, Ribociclib

Detailed description

CLEE011A2408 - No longer available - Managed Access Program (MAP) Cohort to provide access to ribociclib (LEE011, Kisqali®), for locally advanced or metastatic cancer resistant or refractory to available treatment options and candidate for therapy with a CDK inhibitor (including tumors with D-cyclin-CDK4/6-INK4a-Rb pathway abnormalities) CLEE011A2006M - Available - Managed Access Program (MAP) Cohort to provide access to Ribociclib for patients diagnosed with early-stage HR+HER2 (stages II and III) - breast cancer requiring adjuvant treatment with an ET based regimen CLEE011X2001I - Available - Managed Access Program (MAP) Individual patient request to provide access to Ribociclib (in US for liquid formulation only)

Interventions

DRUGRibociclib

Patients receive ribociclib

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
1 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. An independent request was received from a licensed physician. 2. 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. 3. The patient is not eligible or able to enroll in a clinical trial or continue participation in such trial. 4. 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. 5. 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). 6. Provision of the product will not interfere with the initiation, conduct, or completion of a Novartis clinical trial or overall development program. 7. 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.com+41613241111
CONTACTNovartis Pharmaceuticals

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026