So J&J5322, first of all, has an official name now, romantamig, and it is a tri-specific antibody targeting two antigens on the myeloma cell, BCMA and GPRC5D, and then it targets CD3 on the T-cell. And the results we presented are on a Phase one trial, a longer follow-up now than what was presented at ASCO. And what we show is that the response rate’s 100% in BCMA-naive patients...
So J&J5322, first of all, has an official name now, romantamig, and it is a tri-specific antibody targeting two antigens on the myeloma cell, BCMA and GPRC5D, and then it targets CD3 on the T-cell. And the results we presented are on a Phase one trial, a longer follow-up now than what was presented at ASCO. And what we show is that the response rate’s 100% in BCMA-naive patients. The median follow-up now is 14.4 months, and the 12-month PFS is over 80%.
In regards to toxicity, the toxicity profile seems favorable. The grade 3, grade 4 infections plateau after one year of treatment, and also the GPRC-related toxicities in terms of dysgeusia and weight loss seem significantly less than what we’ve seen with talquetamab, the single GPRC-targeting bispecific antibody.
So, you know, also just ease of use – it has a single step-up dose and a Q4-week dosing schedule. So in terms of efficacy, certainly very promising results. In terms of safety, also the signal seems very good. And in terms of options for outpatient dosing and convenience for patients, also it really looks like it has some exciting options.
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