Regeneron's 146.74% Volume Spike Elevates It to 172nd Rank as 1.64% Drop Reflects Pre-Data Market Uncertainty

Generated by AI AgentAinvest Market Brief
Thursday, Jul 31, 2025 9:49 pm ET1min read
REGN--
Aime RobotAime Summary

- Regeneron's stock saw 146.74% volume surge to $0.78B on July 31, 2025, but closed down 1.64% amid pre-data uncertainty.

- Phase 3 OLYMPIA-5 trial tests odronextamab+lenalidomide for relapsed/refractory lymphomas, with July 2025 results potentially reshaping treatment standards.

- Linvoseltamab (REGN5458) Phase 1b trial combines BCMA x CD3 bispecific with daratumumab, aiming to strengthen Regeneron's myeloma position by 2025.

- FDA approved high-dose Eylea to delay biosimilars, while government contracts support revenue stability amid therapeutic innovations.

On July 31, 2025, Regeneron PharmaceuticalsREGN-- (REGN) traded with a volume of $0.78 billion, a 146.74% increase from the previous day, ranking 172nd in market activity. The stock closed down 1.64%, reflecting mixed investor sentiment ahead of key clinical data releases.

Regeneron announced updates to two pivotal oncology trials. The Phase 3 OLYMPIA-5 study is evaluating odronextamab, a bispecific antibody targeting CD20 and CD3, in combination with lenalidomide for relapsed/refractory follicular lymphoma and marginal zone lymphoma. This open-label trial, expected to report primary outcomes by July 2025, could redefine treatment standards if the experimental therapy demonstrates superior efficacy compared to rituximab-based regimens.

Parallel progress was noted in the Phase 1b trial of linvoseltamab (REGN5458), a BCMA x CD3 bispecific antibody being tested for multiple myeloma. The study combines the drug with established therapies like daratumumab and carfilzomib. With recruitment ongoing and an estimated completion date in July 2025, successful outcomes may strengthen Regeneron’s competitive position in hematologic malignancies.

A recent FDA approval for the high-dose version of Eylea (aflibercept) in ophthalmology was highlighted as a potential growth driver, with analysts noting it could delay biosimilar competition. This approval, combined with ongoing government contracts for next-generation antibody therapies, positions the company to sustain revenue streams amid therapeutic advancements.

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