Expanded Access for LOXO-260 in Participants With Cancer Caused by an Abnormal RET Gene That Did Not Respond/is no Longer Responding to Treatment With a Type of Drug Called a RET Inhibitor

Exclusion Criteria

• •Patients tumor must have developed RET solvent front mutations (eg G810X) after RET selective treatment.
• •Have progressed or are intolerant to standard therapy, or no standard therapy option exists, or in the opinion of the investigator, are unlikely to derive significant clinical benefit from standard therapy
• •Have adequate organ function
• •Patients must reside in a country where the LOXO-NGR-21001 study (NCT05241834) is not open or recruiting.
• •Currently enrolled in an ongoing clinical study of LOXO-260 or another second generation RET inhibitor
• •Clinically significant active cardiovascular disease or history of myocardial infarction within 6 months prior to study treatment; ongoing cardiomyopathy; or current prolongation of the QT interval corrected for heart rate using Fridericia's formula (QTcF) interval greater than 470 milliseconds
• •Clinically significant malabsorption syndrome
• •Pregnant or lactating
• •Eastern Cooperative Oncology Group (ECOG) performance status 3 or 4
• •Patients harboring known activating bypass alterations outside RET (eg. EGFR, ALK, RAS etc) that may confer resistance to LOXO-260