Johnson & Johnson Reports Updated Data From Two Early-Stage Multiple Myeloma Studies Of Talvey Combo Treatment

Zinger Key Points
  • RedirecTT-1 Study: 79.5% overall response rate and 52.3% complete response rate for Talvey combined with Tecvayli.
  • TRIMM-2 Study: 82% overall response rate for Talvey plus Darzalex Faspro & pomalidomide, including a 100% response rate in weekly dosing arm

On Friday, Johnson & Johnson JNJ released updated results from the investigational Phase 1b RedirecTT-1 study evaluating the combination of Talvey (talquetamab) and Tecvayli (teclistamab) in patients with relapsed or refractory multiple myeloma.

At data cutoff, 44 patients had been treated with the recommended phase 2 regimen (RP2R) of 0.8 mg/kg of Talvey in combination with 3 mg/kg of Tecvayli every other week.

The overall response rate (ORR) was 79.5%, with a complete response or better (CR+) rate of 52.3%, an 18-month duration of response (DOR) of 85.9%, and an 18-month progression-free survival (PFS) rate of 69.8% with a median follow-up of 18.2 months.

Results from a subgroup analysis of patients with extramedullary disease demonstrated an ORR of 61.1%, with a CR+ rate of 33.3%, an 18-month DOR of 81.8%, and an 18-month PFS rate of 52.9% in patients with EMD at median follow-up 13.6 months.

Johnson & Johnson also revealed updated results from the investigational Phase 1b TRIMM-2 study evaluating the combination of Talvey with Darzalex Faspro and pomalidomide in patients with relapsed or refractory multiple myeloma that demonstrated an ORR of 82%.

At data cutoff, 77 patients had received Talvey in doses of 0.4 mg/kg weekly (QW) or 0.8 mg/kg biweekly (Q2W), with step-up doses combined with Darzalex Faspro and pomalidomide.

In the QW arm (n=18), the overall response rate (ORR) was 100%, with 56 percent having a complete response (CR) or better.

The Q2W arm (n=59) achieved 76% ORR, with 56% achieving CR or better.

The median duration of response (DOR) in the Q2W arm was 26.4 months, and the median progression-free survival (PFS) was 20.3 months.

Results showed that 52% of anti-CD38 refractory patients (n=64) achieved CR or better, and 70.8% received prior chimeric antigen receptor T cell therapy (n=24) achieved CR or better.

Patients who had received prior bispecific antibodies (n=29) achieved an 82.8% ORR.

Price Action: JNJ stock is trading 0.83% higher at $162.73 at the last check on Friday.

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