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Study to evaluate the pharmacokinetics, safety and tolerability of Secukinumab in patients with GCA or PMR

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-507667-19-00
Acronym
CAIN457E22101
Enrollment
24
Registered
2024-05-03
Start date
2024-06-06
Completion date
2025-04-02
Last updated
2025-02-14

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

Conditions

Giant cell arteritis (GCA), Polymyalgia rheumatica (PMR)

Interventions

None listed

Sponsors

Novartis Pharma AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Czechia, Italy, Portugal, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026