>Most commercially available blood cancer patient-derived xenograft (PDX) models are transient in nature, and non-transferable through passages (not renewable), without disease symptoms or mortality. However, Crown Bioscience's PDX models for blood cancer are permanent, and allow the study of disease recurrence after initial treatment challenge and the efficacy testing of novel agents against drug resistance. The Crown Bioscience acute lymphoblastic leukemia (ALL) PDX collection covers a wide range including patient-relevant mutations e.g. BCR/ABL(+). More
PDX offer the most translational preclinical model for efficacy screening in cancer drug development. Derived directly from patient tumors and never adapted to grow in vitro, PDX models reflect the heterogeneity and diversity of the human patient population. PDX give you an accurate, predictive model of how your treatment will perform, well before entering into expensive clinical trials. Crown Bioscience's HuPrime® PDX models are well characterized for pathology, growth characteristics, and are also genetically/genomically annotated for gene expression, gene copy number, mutations, and fusions.
MODEL NUMBER | CANCER TYPE | CANCER SUBTYPE | DESCRIPTION | # per page |
---|---|---|---|---|
AL5503 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL5511 | Acute Lymphoblastic Leukemia | T | AL5511 is an exceptional model designed to propel your research and development efforts in the fight against Acute Lymphoblastic Leukemia (ALL). During the critical pre-clinical phase, it is crucial to have a reliable model that accurately represents the disease and provides valuable insights into the effectiveness of potential oncology drugs. AL5511 offers an unparalleled platform to evaluate the efficacy, safety, and mechanisms of action of your drug candidates, aiding in the identification and optimization of the most promising therapies for ALL patients. Join us as we explore the remarkable capabilities of the AL5511 model, empowering you to make informed decisions and accelerate the development of life-saving oncology treatments. | CLICK TO VIEW |
AL5514 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL5518 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL5521 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7015 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7119 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7142 | Acute Lymphoblastic Leukemia | T | NA | CLICK TO VIEW |
AL7155 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7174 | Acute Lymphoblastic Leukemia | T | NA | CLICK TO VIEW |
AL7267 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7442 | Acute Lymphoblastic Leukemia | T | NA | CLICK TO VIEW |
AL7443 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7447 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL7473 | Acute Lymphoblastic Leukemia | T | NA | CLICK TO VIEW |
AL7475 | Acute Lymphoblastic Leukemia | T | NA | CLICK TO VIEW |
AL8156 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
AL8223 | Acute Lymphoblastic Leukemia | B | NA | CLICK TO VIEW |
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