GLOBAL RESEARCH ARCHIVE
MDX3001 In Vivo CAR-T Generation & B-cell Depletion Data @ASGCT
Research evidence excerpt
MDX3001 In Vivo CAR-T Generation & B-cell Depletion Data @ASGCT
CD3xCD28 targeting dramatically reduced liver uptake while enhancing expression of Form 10Q as of April 17th
the transgene in spleen. In humanized mice, 6ug MDX3001 dose-dependently induced Market Cap. (mil) US$838.2
expression of CD19 CAR-T cells up to 40% in blood and ~35% in the spleen at 6-24 Total Assets ($mil) 1,857
hours. CAR expression was transient accounting for ~20% of splenic T cells at 48 Avg Daily Vol (000) 2,359
Book Value/Share US$1.60 hours and ~0% cells at 72 hours. Despite the transient expression of the CAR, B
Price/Book 69%
cells were almost completely ablated in both blood and spleen for at least 11 days. Net Cash Per Share US$(0.01)
ModeX replicated these findings in NHPs with a CD20 surrogate version of MDX3001, 1Q:26 cash less LTD
and showed that additional doses of MDX3001 could bring the total CAR-T fraction Debt to Total Capital 18.6%
to ~60%. MDX3001 drove impressive T cell expansion up to ~15,000cells/uL. Similar Div Yield 0.00%
to mice, CAR-T drove deep B-cell depletion to ~0 cells/uL in NHPs, before B cells Fiscal Year End Dec
started to repopulate at ~12 days. Dexamethasone did not limit the efficacy of MDX3001,
which is important given that most autoimmune disease patients use steroids as SOC. Price Performance - 1 Year
MDX3001 could enter the clinic this year for autoimmune diseases where transient CAR- USD
T expression achieved by mRNA could be sufficient to produce an immune reset and 1.7
cure disease. 1.6
1.5
RISKS TO ACHIEVEMENT OF PT & RECOMMENDATION
NGENLA, Rayaldee and BioReference may not meet revenue forecast. ModeX's vaccines 1.4
and antibodies may fail in the clinic. OPKO may require additional capital. 1.3
1.2
COMPANY DESCRIPTION
The English excerpt is extracted automatically from the cited source page and may contain layout or recognition errors. It is never batch translated.
Open report viewer