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Zymeworks (ZYME) investor relations material
Zymeworks Wells Fargo 20th Annual Healthcare Conference 2025 summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Zanidatamab partnership and milestones
Phase 3 readout for zanidatamab in gastroesophageal adenocarcinoma expected in late Q4, with initial qualitative PFS data followed by detailed results at a medical meeting.
Regulatory milestones remaining total about $500 million, with $860 million in commercial milestones and royalties ranging from 10% to 20% based on net sales.
Jazz Pharmaceuticals is exploring additional indications, including breast cancer and pan-tumor studies, which could expand the opportunity beyond the current $2 billion base case.
Internal modeling aligns with external analyst estimates of a $2 billion+ opportunity for zanidatamab, with potential for further growth as new indications are pursued.
Pipeline updates and clinical strategy
ZW171 program discontinued due to on-target, off-tumor toxicity at maximum tolerated dose, reflecting a disciplined approach to capital allocation and rapid decision-making.
ZW191, a folate receptor alpha ADC, is enrolling ovarian, endometrial, and non-small cell lung cancer patients in Phase 1, aiming for best-in-class efficacy and tolerability.
ZW191’s antibody demonstrates superior internalization and differentiation from competitors, with potential for expansion into multiple tumor types and combination therapies.
Partnering is a key strategy for advancing assets like ZW191, with decisions on further development or combinations dependent on emerging clinical data.
Early-stage pipeline and platform innovation
ZW251 ADC program has cleared IND and will enter clinical studies by year-end, utilizing the same payload as ZW191.
Additional ADCs and T-cell engager programs, including ZW209 (tri-TCE platform) and ZW1528 (autoimmune, bispecific), are advancing, with ZW209 IND expected in 1H 2026 and ZW1528 in late 2026.
The Azymetric platform enables development of differentiated bispecifics, leveraging protein engineering expertise to target validated and novel mechanisms.
Early-stage programs are prioritized based on business case, target product profile, and strategic fit, with partnering considered for select assets.
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