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ImmunityBio Meets Endpoint In Second Indication Cohort In Bladder Cancer Trial

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ImmunityBio Meets Endpoint In Second Indication Cohort In Bladder Cancer Trial
  • ImmunityBio Inc (NASDAQ: IBRX) has announced that Papillary disease (Cohort B) of its Phase 2/3 study of intravesical BCG plus Anktiva met its primary endpoints with disease-free survival of 57% at 12 months. 
  • Non-muscle invasive bladder cancer (NMIBC) makes up 75%-85% of all bladder cancers in the U.S.; approximately 90% of NMIBC cases are papillary.
  • Related: ImmunityBio Announces Updated Data From Ongoing Bladder Cancer Trial Showing Complete Response Rate Of 72%.
  • To date, 73 patients have enrolled in Cohort B with a median follow-up of 17.3 months. 
  • At 18-months, the disease-free survival rate was 53%. Durable responses were noted.
  • There were zero immune- or treatment-related severe adverse events noted in the combined safety analysis of 154 patients in the trial.
  • Key patent allowed covering Anktiva intravesical use in bladder cancer with the term extending to 2035.
  • Price Action: IBRX shares are up 2.52% at $9.16 during the market session on the last check Tuesday.
 

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Posted-In: bladder cancer Briefs Phase 2 Trial Phase 3 TrialBiotech News Health Care General

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