A Clinical Trial Evaluating the Influence of the Ingredients MyCondro™ and Bovine Chondroitin Sulfate on the Behavior of Cells in the Osteoarticular Sphere

Inclusion Criteria: * Men. * 18-35 years old (terminals included). * Liver test in the reference standards. * Renal assessment in the reference standards. * NFS in the reference standards. * CRP in the reference standards. * Blood pressure compatible with the conduct of the study. * Non-smoker or occasional smoker (\<5 cigarettes/day or \< 10ml per week of electronic cigarette liquid dosed at 3 mg/ml of nicotine). * \< to 5 hours of intense sport per week. * Weight≥ to 60 kg. * BMI between 20 and 28 kg/m² (terminals not included). * Subjects able and willing to comply with the protocol and provide written informed consent. * Subjects affiliated to social security Exclusion Criteria: * All types of vaccination under one month. * Alcohol consumption above WHO standards (\>3 glasses of alcohol per day for men). * Ongoing treatment (medication, dietary supplement or probiotic) and within 4 weeks prior to inclusion. * Known pathology (including seasonal). * Allergy to the study product (all types) * People with a diet that is not suitable for the conduct of the study (e.g. vegetarian, vegan or vegan diet). * Change in eating habits in the 4 weeks prior to inclusion. * Medical and/or surgical history judged by the investigator or his/her representative to be incompatible with the trial. * Blood donation made in the 3 months prior to the inclusion visit or intending to do so during the study. * Persons under guardianship, curatorship, deprivation of liberty, safeguard of justice.…