The MedinCell team has selected the lead formulation and started the regulatory preclinical development of those three programs. The three new programs into regulatory development are: mdc-GRT: organ transplant - molecule: Tacrolimus: This treatment is intended to prevent graft rejection in organ transplant patients. It uses Tacrolimus, an immunosuppressant already widely used, as the active ingredient. In addition, to improve compliance, a major issue in patients who have received a transplant associated with a necessary lifelong treatment, this product could reduce the risk of adverse effects. The regulatory activities that have just begun should make it possible to launch the first-in-human study in 2022. mdc-KPT: pain in animal health - molecule: confidential: The company’s first animal health program, mdc-KPT is a 5- to 7-day treatment targeting acute pain for pets, based on an active ingredient already widely used. The regulatory activities, which have just started, should enable the beginning of the product’s clinical trials before the end of 2021. mdc-TTG: Covid-19 - molecule: Ivermectin: The objective of the company’s mdc-TTG program is to protect humans from Covid-19 and its variants with a long-acting injection of Ivermectin. A first formulation candidate potentially active for more than a month has entered regulatory preclinical development. The context of the pandemic could lead to approval in 2022.