Therapeutic Asset Ratings
3,774 results matching 1 filter
129,767 assets · 8,707 sponsors · 3,128 indications
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Sponsor
Phase
Rating
her2bbζ/cd19t+ t cells
Acute Myeloid Leukemia
David Avigan
P1/2
CCC
(49)
msc11fcd
Glioblastoma
CHA University
P1/2
CCC
(49)
Tcr-T Cells
Hepatocellular Carcinoma
Lion TCR Pte. Ltd.
P1/2
CCC
(49)
Tisagenlecleucel
Leukemia
Stanford University
P1/2
CCC
(49)
Alpha/Beta T Cell-Depleted Hematopoietic Stem Cells
Acute Lymphoblastic Leukemia
Masonic Cancer Center, University of Minnesota
P2
CCC
(48)
Autologous Dendritic Cell/Tumor Antigen, Adcta
Hepatocellular Carcinoma
Chang Gung Memorial Hospital
P2
CCC
(48)
Autologous Hb-Admscs
Multiple Sclerosis
Hope Biosciences Research Foundation
P2
CCC
(48)
Axicabtagene Ciloleucel
Acute Lymphoblastic Leukemia
Novartis Pharmaceuticals
P2
CCC
(48)
Brexucabtagene Autoleucel
Acute Lymphoblastic Leukemia
H. Lee Moffitt Cancer Center and Research Institute
P2
CCC
(48)
Breyanzi Injectable Product
Acute Lymphoblastic Leukemia
Masonic Cancer Center, University of Minnesota
P2
CCC
(48)
cd22/cd19 car-t cell immunotherapy
Lymphoma
Liping Dou
P2
CCC
(48)
cd45ra-depleted dli
Hodgkins Lymphoma
St. Jude Children's Research Hospital
P2
CCC
(48)
cd70.car nk cells
Hodgkins Lymphoma
M.D. Anderson Cancer Center
P2
CCC
(48)
Chimeric Antigen Receptor Modified T Cells Infusion
Mantle Cell Lymphoma
Canadian Cancer Trials Group
P2
CCC
(48)
Cytokine-Induced Memory-Like Nk Cells
Myelodysplastic Syndrome
Washington University School of Medicine
P2
CCC
(48)
Dc-Cik
Melanoma
The First People's Hospital of Changzhou
P2
CCC
(48)
Dendritic Cell Tumor Fusion
Fallopian Tube Cancer
Beth Israel Deaconess Medical Center
P2
CCC
(48)
Descartes-08
Plasma Cell Myeloma
Cartesian Therapeutics
P2
CCC
(48)
Dilanubicel
Acute Biphenotypic Leukemia
Fred Hutchinson Cancer Center
P2
CCC
(48)
Dilanubicel
Myelodysplastic Syndrome With Excess Blasts
Fred Hutchinson Cancer Center
P2
CCC
(48)
Dilanubicel
Myelodysplastic Syndrome With Single Lineage Dysplasia
Fred Hutchinson Cancer Center
P2
CCC
(48)
HUMAN CULTURE EXPANDED GENETICALLY MODIFIED AUTOLOGOUS T CELLS FOR CELL-BASED GENE THERAPY. CELLS ARE DERIVED FROM ISOLATED BLOOD OF THE PATIENT AND ARE TRANSDUCED WITH NON-REPLICATIVE SELF-INACTIVATING (SIN) HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV-1) BASED LENTIVIRAL VECTOR (LVV) PSEUDOTYPED WITH THE VESICULAR STOMATITIS VIRUS GLYCOPROTEIN G (VSV-G) ENVELOPE PROTEIN, AND ENCODING THE C11D5.3 ANTI-TNF RECEPTOR SUPERFAMILY MEMBER 17 (TNFRSF17, BCMA) SINGLE CHAIN VARIABLE FRAGMENT (SCFV) CD8/4-1BB/CD3ZETA CHIMERIC ANTIGEN RECEPTOR (CAR) UNDER THE TRANSCRIPTIONAL CONTROL OF THE MYELOPROLIFERATIVE SARCOMA VIRUS ENHANCER, NEGATIVE CONTROL REGION DELETED, DL587REV PRIMER-BINDING SITE SUBSTITUTED (MND) PROMOTE
Acute Lymphoblastic Leukemia
Masonic Cancer Center, University of Minnesota
P2
CCC
(48)
Igv-001 Cell Immunotherapy
Glioblastoma
Imvax
P2
CCC
(48)
Inaticabtagene Autoleucel
Acute Lymphoblastic Leukemia
First Affiliated Hospital of Zhejiang University
P2
CCC
(48)
Jwcar029
Follicular Lymphoma
Sun Yat-sen University
P2
CCC
(48)
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