GLOBAL RESEARCH ARCHIVE
DMRA: 1Q26: '001 On Track; We Continue to Believe DMRA Has The Optimal Approach To mCALR
Research evidence excerpt
DMRA: 1Q26: '001 On Track; We Continue to Believe DMRA Has The Optimal Approach To mCALR
for DMR-001, DMRA's own mCALR antibody is expected mid-year, setting 2026 (0.62)A (0.48)E (0.54)E (0.59)E
up for initial data in mid-'27. We believe DMR-001's improved properties, Prev. (0.65)E (0.51)E (0.57)E (0.64)E
including half-life extension through YTE Fc modifications, convenient All values in USD unless otherwise noted.
potential Q4W subQ dosing, and potentially narrower relative potency Priced as of prior trading day's market close, EST (unless otherwise noted).
against type 1 and non-type 1 CALR mutations all serve to address INCY's
'989 shortcomings, in our view, even if the latter may be eventually
formulated as an on-body injector, which may have associated challenges
of its own. The co highlighted a potential ph.I design with starting doses
closer to therapeutic levels, which could additionally enable signal finding
much earlier on, especially honing in on the right dose that leads to non
type-1 efficacy. DMRA's EHA abstract largely recapitulates data that we
have seen before, though may include additional reporter assay data on
downstream signaling inhibition in both type 1 and type 2 CALR models,
which could support improved relative potency for '001 in these subtypes.
Recent competitor updates favorable for DMRA, in our view. INCY's EHA
update today further supports CALR as a validated target across both 2L
MF and ET, and earlier alignment with the FDA on a shorter, 24-week
registrational program in ET vs. traditionally 52 weeks should have positive
readthroughs to DMRA's own development path, as it could potentially
help shave some time off of timelines and importantly, have the Agency be
familiar with the MoA and associated endpoints before DMRA has to align
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