This is an expanded access program (EAP) designed to provide access to Botensilimab and Balstilimab prior to drug registration by the applicable local regulatory agency. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.
The patient's disease is serious or life-threatening.
The patient has undergone appropriate standard treatments; there are no comparable or satisfactory alternative treatments for the disease or condition; the treatment is adjunct to an existing treatment option, and the treatment is not medically contra-indicated.
Sufficient efficacy and safety evidence exists to make a benefit-risk analysis consistent with this policy and the potential patient benefit justifies any potential risks of treatment.
Sufficient clinical data are available to identify an appropriate dose and treatment duration.
None
Botensilimab
DrugAdministered via an intravenous (IV) infusion of Botensilimab + Balstilimab combination (BOT+BAL).
Balstililmab
DrugAdministered via an IV infusion of Botensilimab + Balstilimab combination (BOT+BAL).
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