Oppenheimer analyst Matthew Biegler notes that on Monday, Nurix Therapeutics unveiled first-in-human data from its second-generation BTK degrader, NX-5948. The good news is that the drug looks safer than NX-2127, Oppenheimer says. There were few Grade 3 or higher adverse events, and no patients had discontinued treatment as of the cutoff-and dose escalation is ongoing. Better safety would jibe with the theory that dialing out NX-2127’s IMiD activity should improve tolerability without sacrificing efficacy-at least in the CLL subset of patients, it adds. Unfortunately, efficacy was still quite early in this data set, the firm acknowledges. Only one patient had prior pirtobrutinib exposure, and none had the tell-tale C481S mutant that predicts poor response to ibrutinib. Without any real data from patients in relevant treatment categories, it’s hard to say how NX-5948 stacks up against the competition, Oppenheimer argues. The firm has an Outperform rating on the shares.
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Read More on NRIX:
- Nurix Therapeutics Presents Positive Clinical Data from Its Novel Bruton’s Tyrosine Kinase (BTK) Degrader Programs, NX-5948 and NX-2127, at the 65th American Society of Hematology (ASH) Annual Meeting
- Nurix Therapeutics Announces Webcast To Review Data from Its Phase 1 Clinical Trials of BTK Degraders, NX-5948 and NX-2127, Presented at the 65th American Society of Hematology (ASH) Annual Meeting
- Nurix Therapeutics price target lowered to $9 from $12 at Morgan Stanley
- Nurix Therapeutics Announces Presentations at the 65th American Society of Hematology (ASH) Annual Meeting
- FDA puts partial clinical hold on Nurix’s Phase 1 NX-2127-001 study