Compassionate Use
We believe that the best way for patients to access investigational medicines is through a clinical trial. Our clinical trials are listed at ClinicalTrials.gov and include eligibility criteria. If you are interested in learning whether enrollment in a clinical trial is an option for you or someone you know, please consult with the treating physician, who can contact us as needed with questions.
When enrollment in a clinical trial is not an option, and all currently available treatment options have been tried, an investigational medicine may be provided before it is commercially available under programs called Expanded Access or Compassionate Use, which are regulated by the US Food and Drug Administration. Investigational medicines provided by Tango under these circumstances will always be given in accordance with applicable laws and regulations.
Currently, our program is restricting enrollment to patients who are responding to or benefitting from treatment on closing Tango studies, who would otherwise lose access to their current treatment at time of study closure.
We recognize the urgency faced by patients with limited treatment options. We hope to expand our access, at a time in which doing so will not compromise ongoing clinical trials, regulatory submissions, or our ability to develop therapies for broader patient populations. We will regularly reassess our policy as clinical development progresses and regulatory landscapes evolve.
All Compassionate Use requests should come from a treating physician (compassionateuse@tangotx.com). We answer all such requests as soon as possible (but in any event, within five business days). Physicians who administer Tango investigational medicines through a Compassionate Use program must comply with all applicable laws and regulations and contractual conditions, including those relating to safety reporting.