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Oncolytics Biotech

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FDA written feedback supports a potential accelerated-approval strategy for Oncolytics’ REO 033 using response rate and duration, but the company must first generate supportive randomized Part A data before moving toward a pivotal expansion. Representative image.
Pharma & Biotech

Oncolytics says FDA opens a possible accelerated-approval route for pelareorep in RAS-mutant colorectal cancer

FDA written feedback supports a potential pivotal expansion of REO 033 using response rate and duration as an accelerated-approval strategy, but Oncolytics must first generate supportive randomized Part A data.

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A representative image illustrating Oncolytics Biotech’s pelareorep colorectal cancer research as FDA feedback outlines a potential accelerated approval path in second-line RAS-mutant, microsatellite-stable metastatic colorectal cancer.
Pharma & Biotech

Pelareorep gets clearer FDA path toward accelerated approval in RAS-mutant colorectal cancer

FDA feedback could let pelareorep move directly into a pivotal colorectal cancer expansion if randomized REO 033 data support accelerated approval.

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Pharma & Biotech

Why Oncolytics Biotech’s new GOBLET cohort 4 data matters for third-line anal cancer immunotherapy strategies

Find out why Oncolytics Biotech’s latest GOBLET cohort 4 data could reshape immunotherapy strategies for third-line anal cancer.

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