Skip to content

Managed Access Programs for AIN457, Secukinumab

Managed Access Programs for AIN457, Secukinumab

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT05583604
Enrollment
Unknown
Registered
2022-10-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-18

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

Conditions

Hidradenitis Suppurativa (HS)

Keywords

MAP, Manage Access Program, Hidradenitis suppurativa (HS), AIN457, secukinumab, Cosentyx

Brief summary

The purpose of this registration is to list Managed Access Programs (MAPs) related to AIN457, secukinumab

Detailed description

CAIN457M2002M - Available - Managed Access Program (MAP) Cohort Treatment Plan CAIN457M2002M to provide access to Secukinumab for adult and adolescent patients with Hidradenitis Suppurativa (HS)

Interventions

DRUGsecukinumab

Patients receive secukinumab

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Eligibility

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

Inclusion criteria

* An independent request should be received from a licensed physician (in some instances from Health Authorities, Institutions or Governments). * The patient has a serious or life-threatening disease or condition and no comparable or satisfactory alternative therapy is available for diagnosis, monitoring or treatment; patient is not medically eligible for available treatment alternatives or has exhausted all available treatment options. * The patient is not eligible or able to enroll in a Novartis clinical trial or continue participation in a Novartis clinical 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 a country (as applicable). * Provision of the product will not interfere with the initiation, conduct or completion of a Novartis clinical trial or overall development program.

Contacts

Primary 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
Backup ContactNovartis Pharmaceuticals
+41613241111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026