Oncternal Therapeutics Reports Patient Death In Mid-Stage Blood Cancer Study Treated With Second Dose Level

Zinger Key Points
  • The first patient treated at the second dose level experienced fatal adverse event.
  • At the initial dose two of the three patients achieved complete metabolic response, and the third achieved a partial response.

Oncternal Therapeutics Inc ONCT updated the status of a recent study involving a treatment for relapsed or refractory aggressive B-cell lymphoma, including patients who have failed previous CD19 CAR-T treatment.

The dose-escalation/dose-expansion Phase 1/2 Study ONCT-808-101 evaluates the company's ROR1-targeting autologous CAR T cell therapy ONCT-808.

At the initial dose of 1x106 CAR T cells per kg, two of the three patients achieved complete metabolic response (CMR), and the third achieved a partial response (PR) by FDG PET-CT. 

The common adverse events in this dosing cohort included decreased blood counts, pneumonia, and Grade 1-2 cytokine release syndrome (CRS) as of a Dec. 4, 2023 data cutoff.

The first patient treated at the second dose level of 3x106 CAR T cells per kg, an 80-year-old with bulky disease who had received four previous lines of therapy including CD19 CAR T, experienced a Grade 5 (fatal) serious adverse event consistent with CRS and immune effector cell-associated neurotoxicity syndrome (ICANS). 

No evidence of his lymphoma was found histologically, based on the patient's initial autopsy report.

Oncternal has been in communication and is aligned with the FDA on proposed protocol changes that include modified eligibility criteria and testing lower doses of ONCT-808 for future patients in the study.

Price Action: ONCT shares are down 23.1% at $0.46 on the last check Tuesday.

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