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DRUG:

tesevatinib (KD019)

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Other names: KD-019, KD019 , XL647, XL 647, PRIM-001 , XL7647
Company:
Sanofi
Drug class:
EGFR inhibitor, HER2 inhibitor, VEGFR inhibitor, EphB4 inhibitor
Related drugs:
3years
In vivo efficacy of tesevatinib in patient-derived xenograft glioblastoma models may be limited by tissue binding and compensatory signaling. (PubMed, Mol Cancer Ther)
Overall, tesevatinib efficacy in EGFR amplified PDX GBM models is robust in vitro but relatively modest in vivo, despite a high brain-to-plasma ratio. This discrepancy may be explained by drug-tissue binding and compensatory signaling.
Preclinical • Journal
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ABCB1 (ATP Binding Cassette Subfamily B Member 1)
|
EGFR amplification
|
tesevatinib (KD019)
almost4years
Study of Tesevatinib Monotherapy in Patients With Recurrent Glioblastoma (clinicaltrials.gov)
P2, N=40, Completed, Kadmon Corporation, LLC | Active, not recruiting --> Completed
Clinical • Trial completion
|
EGFR (Epidermal growth factor receptor)
|
EGFR amplification
|
tesevatinib (KD019)
4years
Study of Tesevatinib Monotherapy in Patients With Recurrent Glioblastoma (clinicaltrials.gov)
P2, N=40, Active, not recruiting, Kadmon Corporation, LLC | Trial primary completion date: Jan 2020 --> Mar 2020
Clinical • Trial primary completion date
|
EGFR (Epidermal growth factor receptor)
|
EGFR amplification
|
tesevatinib (KD019)
over4years
Study of Tesevatinib in Subjects With Non-Small Cell Lung Cancer, EGFR Activating Mutation, Prior Treatment With a Tyrosine Kinase Inhibitor, and Brain Metastases or Leptomeningeal Metastases (clinicaltrials.gov)
P2, N=36, Completed, Kadmon Corporation, LLC | Trial completion date: Aug 2018 --> Jan 2019 | Trial primary completion date: Aug 2018 --> Jan 2019
Clinical • Trial completion date • Trial primary completion date
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EGFR (Epidermal growth factor receptor)
|
EGFR mutation • EGFR L858R • EGFR exon 19 deletion • EGFR T790M
|
tesevatinib (KD019)