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Tuesday, December 05, 2023 7:05:46 PM
"1852 Cytokine and Mutation Profiling Reveal Patterns of Complete Remission Rates with Lenzilumab Combination Therapy in Chronic Myelomonocytic Leukemia."
https://ash.confex.com/ash/2023/webprogram/Paper179706.html
This is in stark contrast to what Gilead achieved using magrolimab.
"Gilead To Discontinue Phase 3 ENHANCE Study of Magrolimab Plus Azacitidine in Higher-Risk MDS"
https://www.gilead.com/news-and-press/press-room/press-releases/2023/7/gilead-to-discontinue-phase-3-enhance-study-of-magrolimab-plus-azacitidine-in-higher-risk-mds
And of course, since our results were already published in the 'blood' journal, our presentation should be well-received.
https://ashpublications.org/blood/article/142/Supplement%201/1847/505640/Lenzilumab-in-Addition-to-Azacitidine-Improves
In addition, we know that this indication offered certain regulatory incentives. Will our demonstrated success result in an expedited approval or the award of a Priority Review Voucher? If so, will Humanigen announce that news this week, ahead of the conference, and perhaps with the announcement of the recall of our loaned shares?
Also, I see that another of our trial doctors, Dr. Saad Kenderian, who was also very excited about lenzilumab's performance in the LIVE-AIR trial, will also be moderating a separate presentation on Immunotherapies.
https://ash.confex.com/ash/2023/webprogram/Session24628.html
I hope shareholders can begin to see the long-awaited benefit of our faith In Humanigen, and in lenzilumab. It certainly looks promising.
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