Friday, December 08, 2017 12:28:32 PM
Leukocyte Interleukin injection are also tested in H&N in a P2 by another Co, IRX Therapeutics and showed effectiveness:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300054/figure/F6/
This trial and this drug is a pretty perfect copy of the CVM trial and of Multikine, and they spent several tens of million for the Co and for the trials, which prove that there is something of interesting in this choice.
https://clinicaltrials.gov/ct2/show/NCT02609386
Obviously it's extremely hard to know how close is CVM trial to 10% of reduction, by inference, it seems that they would be safe with a 6% ,having regard to their request submitted to the FDA. How conservative was it?
IMO: I hope that also a reduction around 6-9% (that is not a poor result in cancer!) could lead to a negotiation with FDA.
Recent CVM News
- Form S-3/A - Registration statement under Securities Act of 1933: [Amend] • Edgar (US Regulatory) • 10/30/2024 09:21:00 PM
- Form S-3 - Registration statement under Securities Act of 1933 • Edgar (US Regulatory) • 10/25/2024 09:17:48 PM
- FDA’s Oncologic Drugs Advisory Committee Decision on Checkpoint Inhibitors Substantiates Potential of CEL-SCI’s Multikine® to Address Major Treatment Gap for PD-L1 Negative Cancer Patients • Business Wire • 10/22/2024 01:15:00 PM
- Form AW - Amendment Withdrawal Request • Edgar (US Regulatory) • 10/10/2024 08:05:19 PM
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- CEL-SCI Selects Ergomed as CRO as it Gears Up for Confirmatory FDA Registration Study of Multikine® in Head and Neck Cancer • Business Wire • 10/01/2024 10:00:00 AM
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- Form S-8 - Securities to be offered to employees in employee benefit plans • Edgar (US Regulatory) • 08/30/2024 08:32:13 PM
- CEL-SCI Corporation Reports Third Quarter Fiscal 2024 Financial Results • Business Wire • 08/15/2024 12:00:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2024 08:27:32 PM
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