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Feasibility and Safety Assessment of a Combined Advanced Therapy Medicinal Product Based on A Polymeric Medical Device Combined to Autologous Bone Marrow-Derived Mesenchymal Stem Cells in Hydrogel Mixture for The Treatment of Knee Femoral Cartilage Isolated Lesions

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-512977-28-01
Acronym
LAMINA.ONE
Enrollment
6
Registered
2024-10-09
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-05

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

Conditions

Patients with knee femoral cartilage isolated lesions

Interventions

None listed

Sponsors

Lamina Therapeutics
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

France

Outcome results

None listed

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