John McAdory
appointed John McAdory as Chief Operating Officer of the Company
Highest-materiality recent filing
Oncolytics: FDA Type D meeting in Aug; half of REO 033 sites activated, >20 patients pre-identified
Company to hold Type D meeting with FDA in first half of August 2026 to discuss registrational design for REO 033 Part B.
Oncolytics Biotech disengages EY, engages Baker Tilly as auditor after restructuring
Audit committee voted to disengage EY and engage Baker Tilly for fiscal 2026, subject to client acceptance.
USPTO issued patent covering pelareorep manufacturing process, expected protection into 2044.
Oncolytics appoints Steve Glover to board, promotes John McAdory to COO
Steve Glover appointed to board effective June 1, 2026; he chaired Ambrx during its $2B J&J acquisition.
Initial data in solid tumor model shows greater anti-tumor activity with pelareorep+RAS inhibitor vs either alone.
Data from GOBLET (advanced pancreatic cancer) and AWARE-1 (early-stage breast cancer) to be presented at ASCO 2026 May 29-June 2.
Oncolytics reports 19.5-month median DOR in 2L RAS-mutant MSS mCRC; triples ORR vs SOC
Pelareorep-based combo shows median duration of response 19.5 months in 2L KRAS-mutant MSS mCRC, vs historical 4–6 months.
Oncolytics secures FDA alignment on pivotal anal cancer study for pelareorep
FDA agreed on a randomized controlled pivotal trial design for pelareorep in post-first-line metastatic SCAC, targeting accelerated and full approval.
Oncolytics Biotech enters ATM agreement for up to $75M common stock offering
Agreement with Jefferies LLC allows sale of up to $75M in common stock at market prices.
Oncolytics schedules Type C FDA meeting for pelareorep single-arm study in anal cancer
FDA meeting set for April 16, 2026 to discuss single-arm pivotal study of pelareorep + checkpoint inhibitor in SCAC.
Redomestication from Canada to Nevada completed; common stock continues trading on Nasdaq under ONCY.
Oncolytics completes continuance to BC; expects Nevada domestication by March 31
First step completed March 17: continuance from Alberta to British Columbia under BCBCA.
Pelareorep data at AACR: 62% ORR in pancreatic cancer; TLS formation in breast cancer
GOBLET cohort 1: 62% objective response rate in first-line mPDAC, more than double historical chemotherapy alone.
Randomized Phase 2 study (REO 033) of pelareorep + bevacizumab + FOLFIRI vs bevacizumab + FOLFIRI in 30 patients per arm.
Oncolytics prioritizes SCAC and CRC registration studies; GOBLET enrollment closed
Concluded enrollment in GOBLET gastrointestinal study; now focusing on registrational studies in squamous cell anal cancer (SCAC) and metastatic colorectal cancer (CRC).
FDA Fast Track Designation for pelareorep + bevacizumab + FOLFIRI in second-line KRAS-mutant MSS metastatic colorectal cancer.
Oncolytics appoints EVP John McAdory and VP Biostatistics Yujun Wu, grants inducement awards
John McAdory named EVP Strategy & Operations; previously VP Clinical Ops at CG Oncology (Nasdaq: CGON).
Oncolytics shareholders OK continuance to BC and domestication to Nevada
Continuance from Alberta to British Columbia approved: 85.21% in favor.
GOBLET Cohort 4: 4/14 evaluable third-line anal cancer patients responded (ORR 29%), 2 CRs, 2 PRs; median DOR ~17 months vs historical ~10%.
appointed John McAdory as Chief Operating Officer of the Company
appointed Stephen Glover as the ninth director of the Board
Max materiality 0.85 · Median 0.65 · Most common event other_material