Roche Receives FDA Accelerated Approval for Lunsumio VELO
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Dec 22 2025
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Should l Buy ?
Source: NASDAQ.COM
FDA Approval: Roche's Lunsumio VELO (mosunetuzumab) has received FDA approval as a subcutaneous treatment for adult patients with relapsed or refractory follicular lymphoma after two or more lines of systemic therapy, based on phase I/II study results.
Treatment Efficiency: The new formulation allows treatment to be administered in just one minute, significantly reducing the time patients spend in the clinic and catering to their individual needs and preferences.
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About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.





