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The FDA has now allowed Eli Lilly's treatment for use in adults with untreated leukemia.

TrialRead the original at Benzinga
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The FDA's new first-line approval gives Lilly access to another group of leukemia patients, and study results favored Jaypirca over the comparison treatment. The approval covers only adults without a known 17p deletion, and the story gives no sales estimate or safety findings.

LLY · Eli Lilly and Co.

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The AI's read

This gives Lilly another group of patients who may receive Jaypirca earlier in their treatment. The study found responses in 94% of patients, and the comparison group's median time before disease worsened was 33.5 months; Jaypirca's had not yet been reached. The approval applies only to adults without a known 17p deletion. The story gives no sales estimate or safety findings, but the approval and study results make this positive for Lilly.

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