Zymeworks Inc

News & Events zu Zymeworks Inc (ZYME)

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10/27 07:30

Faeth Therapeutics Appoints Adam Schayowitz to Board of Directors

Faeth Therapeutics (FTH) announced the appointment of Adam Schayowitz, Ph.D., MBA, to its Board of Directors. Dr. Schayowitz is Executive Vice President and Head of Research and Development at Zymeworks (ZYME).

10/25 17:00

Zymeworks Presents ZW191 Clinical Data at ESMO 2026

Zymeworks presented new clinical data from the randomized dose-optimization portion of its ongoing Phase 1 study evaluating ZW191, a FRalpha-targeting antibody-drug conjugate, ADC, at the European Society for Medical Oncology, ESMO, Congress 2026 in Madrid, Spain. The presentation highlights compelling anti-tumor activity in heavily pretreated patients with platinum-resistant ovarian cancer, including patients with high-grade serous disease across all levels of FRalpha expression. Key highlights: ZW191 demonstrates compelling anti-tumor activity in heavily pretreated patients with platinum-resistant ovarian cancer across folate receptor alpha expression levels; Confirmed objective response rates of 64.5% at the 6.4 mg/kg dose in patients with high-grade serous platinum-resistant ovarian cancer; Median duration of response not yet reached at either dose level at median 7 months follow-up, with six-month progression-free survival rate of 61% in both groups; Favorable tolerability profile, particularly at 6.4 mg/kg, supports continued clinical development in partnership or through a strategic collaboration

10/25 16:30

Zymeworks Presents ZW191 Clinical Data at ESMO 2026

Zymeworks presented new clinical data from the randomized dose-optimization portion of its ongoing Phase 1 study evaluating ZW191, a FRalpha-targeting antibody-drug conjugate, ADC, at the European Society for Medical Oncology, ESMO, Congress 2026 in Madrid, Spain. Key highlights: ZW191 demonstrates compelling anti-tumor activity in heavily pretreated patients with platinum-resistant ovarian cancer across folate receptor alpha expression levels; Confirmed objective response rates of 64.5% at the 6.4 mg/kg dose in patients with high-grade serous platinum-resistant ovarian cancer; Median duration of response not yet reached at either dose level at median 7 months follow-up, with six-month progression-free survival rate of 61% in both groups; Favorable tolerability profile, particularly at 6.4 mg/kg, supports continued clinical development in partnership or through a strategic collaboration

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