• Median follow-up for duration of response was 17.5 months measured from time of first response
The efficacy of JEMPERLI was investigated in a global, nonrandomized, multicenter, multiple cohort, open-label study of 209 patients with dMMR recurrent or advanced solid tumors who had progressed following systemic therapy and had no satisfactory alternative treatment options.* Patients received JEMPERLI 500 mg via intravenous infusion every 3 weeks for 4 doses followed by 1000 mg every 6 weeks until disease progression or unacceptable toxicity.