Iron and its alloys have been widely used for variety of medical implants. These are used for long term applications as cheap implants with high inertness and low corrosion rate, and also as implants with high biocompatibility (the fourth-generation type). Such degrading implants can provide a temporary scaffold while the body heals. In addition to the needed mechanical support, it is highly desirable to provide local drug therapy, providing antibacterial properties, preventing rejection of the implant, and more. So far, the combination of a degradable metallic implant which serves also as a threedimensional matrix for drug release, remained un-answered. Here we present, we believe for the first time realization of this concept: Entrapment of drugs within a 3D degradable metal matrix-ironfrom which the entrapped drugs are sustain-released. This new type of material is based on the molecular metals entrapment materials methodology, resulting in drugs@Fe. Two drugs have been successfully entrapped and released: chlorhexidine -an antiseptic drug, and rapamycin-used for avoiding transplant rejection. The delivery profiles of the composites were studied in two formspowders and pressed discs showing two different types of drug release profiles. The release of the drugs from the powder hasa first order release profile, while the pressed disk is a slower, zero-order release profile, which is highly desirable due to the constant rate of the release. Full characterization of the metallic biomaterials is provided, including XRD, SEM, TGA, elemental analysis, and surface area/ porosity analysis.