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Updated: May 31, 2026

Intracellular Phosphoflow Cytometry of Acute Myeloid Leukemia Patient-Derived Xenotransplants
Published on: June 6, 2025
Phase Ia study to evaluate RO7497987, a FLT3L-fragment Fc fusion protein, in healthy volunteers
Anthony J Iacovelli1, Shomyseh Sanjabi1, Sharareh Monemi1
1Genentech, Inc., South San Francisco, CA, United States.
Background:
Dendritic cells play a critical role in immunity. Fms-related tyrosine kinase 3 ligand (FLT3L) is a cytokine that can promote the expansion and differentiation of bone marrow dendritic cells (DC) progenitors. RO7497987 (FLT3L-Fc) is a novel FLT3 agonist developed to extend the half-life of FLT3L and induce expansion of peripheral blood DC.
Methods:
This Phase Ia trial evaluated the safety, tolerability, pharmacokinetics, and pharmacodynamics of RO7497987 in healthy volunteers. Forty-four participants received RO7497987 as a single ascending dose (SAD, 0.7-70 mg) or multiple ascending doses (MAD, 7 or 21 mg, 21 days apart).
Results:
RO7497987 was safe and well-tolerated at all doses. The most common treatment-related adverse events (AE) were Grade 1 myalgia, headache, and lymphadenopathy, all of which resolved spontaneously. There were no Grade ≥ 3 AEs, serious AEs, or dose-limiting adverse events. Pharmacokinetic analysis showed dose-dependent increases in FLT3L-Fc Cmax and AUCinf with no accumulation in the MAD cohorts. RO7497987 administration resulted in dose-dependent expansion of monocytes, as well as expansion of all major DC subsets, including conventional and plasmacytoid DC, which was sustained with multiple doses.
Conclusion:
These findings aid the design of dosing regimens of RO7497987 as an immunomodulatory agent.
Clinical Trial Registration:
https://www.isrctn.com/ISRCTN92655801, identifier ISRCTN92655801.
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