Nanochon Chondrograft First in Human Early Feasibility Study - Panama
Summary
NIH has registered a First in Human early feasibility study for the Nanochon Chondrograft Implant, a device intended as a primary surgical treatment for adult patients with knee cartilage lesions. The single-arm study will enroll males and females aged 22 to 60 and is registered under NCT07542184.
What changed
NIH registered a new clinical trial on ClinicalTrials.gov for the Nanochon Chondrograft Implant, a device under early feasibility evaluation as a primary surgical treatment for knee cartilage lesions. The study will enroll adult participants between ages 22 and 60 in Panama.
Affected parties include clinical investigators and sponsors conducting device trials in the knee cartilage space. This registry entry is informational and does not itself impose compliance obligations, though it signals ongoing clinical activity in cartilage repair devices.
Archived snapshot
Apr 21, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Nanochon Chondrograft First in Human (FIH) Early Feasibility Study (EFS) - Panama
N/A NCT07542184 Kind: NA Apr 21, 2026
Abstract
The goal of this First in Human study is to learn if the Nanochon Chondrograft Implant is a safe primary surgical treatment for participants with cartilage lesions in the knee. This study will include males and females between the ages of 22 and 60.
Conditions: Knee Cartilage Lesions
Interventions: Nanochon Chondrograft
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