Achilles Therapeutics is committed to developing precision tumor-derived T cell therapy targeting clonal cancer neoantigens. Our current therapies are considered investigational, which means that they have not been approved as safe and effective by regulatory health authorities, such as the United States Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
Expanded Access is a potential pathway for a patient with an immediately life-threatening condition or serious disease or condition to gain access to an investigational drug for treatment outside of a clinical trial when no comparable or satisfactory alternative therapy exists. Per FDA, Expanded Access may be appropriate when all the following apply:
Achilles Therapeutics is not currently making any of its investigational medicines available on an Expanded Access basis prior to regulatory approval anywhere in the world.
Achilles Therapeutics may revise this Expanded Access Policy at any time and will publish the revised policy accordingly. The posting of this policy by Achilles Therapeutics shall not serve as a guarantee of access to any specific investigational medicine by any individual patient.
This Expanded Access Policy is being posted pursuant to Section 3032 of the 21st Century Cures Act and section 561 of the United States Food, Drug, and Cosmetics Act, as amended.
If you have additional questions, patients should speak with your treating physician. Physicians can contact Achilles Therapeutics via info@achillestx.com.