Ytracis is a solution containing the active substance yttrium radioactive form of the chemical element yttrium.
|Table of Contents|
|What is it used for?|
|How is it used?|
|How does it work?|
|How has it been studied?|
|What benefits has it shown during the studies?|
|What is the risk associated?|
|Why has it been approved?|
Ytracis is used for radiolabelling. Radiolabelling is a technique where a substance is tagged (labelled) with a radioactive compound. In the case of Ytracis, the product is used to label medicines that have been specially developed for use with the active ingredient yttrium ( 90Y) chloride. These medicines act as carrier to take the radioactivity to where it is needed. These may be substances such as antibodies that have been designed to recognise a particular type of cells in the body, including tumour cells. The effects of the medicine that is radiolabelled with Ytracis will be fully explained in its Package Leaflet.
The medicine can only be obtained with a prescription.
Ytracis will only be handled and given by people who have experience in the safe handling of radioactive material.
Ytracis is never given on its own. It must be mixed outside the body, usually in a laboratory, with the medicine that needs radiolabelling. The 90Y contained in Ytracis then attaches itself to the carrier medicine and the resulting mixture is given according to the instructions in the Package Leaflet of the carrier medicine. The quantity of Ytracis needed for radiolabelling and the quantity of the radiolabelled medicine that is given will depend on the medicine that is radiolabelled and the disease that is being treated.
The active substance in Ytracis, yttrium ( 90Y) chloride, is a radioactive compound. It emits beta radiation. The effect of Ytracis depends on the nature of the carrier medicine that is radiolabelled with Ytracis. An example of its use is the treatment of some types of tumours, where the radiolabelled medicine carries the radioactivity to the site of a tumour. Once there, the radioactivity from Ytracis helps to destroy the tumour.
As Ytracis is a ?precursor? and will not be given on its own, no studies have been done in humans. The company presented information from scientific articles already published on 90Y. The company also presented published information supporting the use of 90Y in radiolabelling other medicines.
The information supplied by the company supports the use of Ytracis as a precursor for radiolabelling medicines with 90Y.
As Ytracis is a precursor and will not be given on its own, it has no side effects. Patients may experience side effects following the injection of the medicine radiolabelled with Ytracis. These side effects will depend on the medicine being used, and they will be described in the Package Leaflet of the medicine labelled with Ytracis. Ytracis is radioactive and its use may carry a risk of cancer and hereditary defects. The doctor who prescribes Ytracis must ensure that the risks linked to the radioactive exposure are lower than the risks from the disease itself.
Ytracis must not be given directly to any patient. Medicines radiolabelled with Ytracis should not be used in people who may be hypersensitive (allergic) to yttrium chloride or any of the other ingredients. A medicine labelled with Ytracis should not be used in women who are or may be pregnant. More information on the restrictions for the medicines radiolabelled with Ytracis will be given in the Package Leaflet of the particular medicine that is radiolabelled with Ytracis.
The Committee for Medicinal Products for Human Use (CHMP) decided that Ytracis?s benefits are greater than its risks for the radiolabelling of carrier molecules which have been specifically developed and authorised for radiolabelling with this radionuclide. The Committee recommended that Ytracis be given marketing authorisation.