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AbbVie Presents Results of Imbruvica (ibrutinib) + Venclexta/Venclyxto in P-III GLOW Study as 1L Treatment for CLL or SLL at EHA 2021

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AbbVie Presents Results of Imbruvica (ibrutinib) + Venclexta/Venclyxto in P-III GLOW Study as 1L Treatment for CLL or SLL at EHA 2021

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  • The P-III GLOW study evaluates Imbruvica + Venclexta/Venclyxto (I+V) vs chlorambucil + obinutuzumab (C+O) in 211 patients in a ratio (1:1) aged ≥65yrs. with CLL/SLL
  • The study met its 1EPs of PFS as assessed by IRC & showed a 78% reduction in risk of disease progression or death- mPFS (not reached vs 21mos.) & safety profile of the combination was consistent with the safety profile of monothx. & tolerability profiles were consistent with CLL treatment in a patient population
  • The 2EPs includes uMRD (51.9% vs 17.1%) @3mos.- PB uMRD (49% vs 12%) @12mos.- CR rate (38.7% vs 11.4%)- ORR was not different b/w treated groups- time to subsequent therapy was longer for I+V

  | Ref: Abbvie | Image: abbvie

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