Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Gloria Patrick"'
Publikováno v:
Cancer Research. 82:CT204-CT204
Background: KRAS is mutated (mt) in 25% of non-small cell lung cancer (NSCLC) adenocarcinoma, with KRAS G12C mt occurring in ~13% of patients. The G12C inhibitor (G12Ci) sotorasib has recently received FDA approval for patients with KRAS G12C mt NSCL
Autor:
Ramaswamy Govindan, Mark M. Awad, Shirish M. Gadgeel, Jonathan A. Pachter, Gloria Patrick, Louis J. Denis
Publikováno v:
Journal of Clinical Oncology. 40:TPS9148-TPS9148
TPS9148 Background: KRAS is mutated (mt) in 25% of non-small cell lung cancer (NSCLC) adenocarcinoma, with KRAS G12C mt occurring in ̃13% of patients. The G12C inhibitor (G12Ci) sotorasib has recently received FDA approval for patients with KRAS G12
Autor:
D. Ross Camidge, Joshua E. Reuss, Alexander I. Spira, Pasi A. Janne, Muneeb Rehman, Jonathan A. Pachter, Gloria Patrick, Louis J. Denis, David R. Spigel
Publikováno v:
Journal of Clinical Oncology. 40:TPS9147-TPS9147
TPS9147 Background: KRAS is mutated (mt) in 25% of NSCLC adenocarcinoma, with KRAS G12V and G12C mt occurring in ̃7% and ̃13% of patients (pts), respectively. Whereas G12C inhibitors have demonstrated promising activity in pts with KRAS G12C NSCLC,
Autor:
Susana N. Banerjee, Bradley J. Monk, Els Van Nieuwenhuysen, Kathleen N. Moore, Ana Oaknin, Michel Fabbro, Nicoletta Colombo, David M. O'Malley, Robert L. Coleman, Amit M. Oza, Jonathan A. Pachter, Gloria Patrick, Louis J. Denis, Lorna Leonard, Rachel N. Grisham
Publikováno v:
Journal of Clinical Oncology. 40:TPS5615-TPS5615
TPS5615 Background: Low-grade serous ovarian cancer (LGSOC) constitutes up to 10% of all ovarian cancer and has clinical and molecular characteristics distinct from high-grade serous ovarian cancer. Approximately a third of patients (pts) with recurr
Publikováno v:
Molecular Cancer Therapeutics. 20:P048-P048
Background: VS-6766 is a unique small molecule inhibitor of both RAF and MEK. In contrast to several other MEK inhibitors available, VS-6766 blocks both MEK kinase activity and RAF phosphorylation of MEK. This sequential blockade mechanism enables VS
Autor:
Susana N. Banerjee, Bradley J. Monk, Els Van Nieuwenhuysen, Kathleen N. Moore, Ana Oaknin, Michel Fabbro, Nicoletta Columbo, David M. O’Malley, Robert L. Coleman, Jonathan Pachter, Andrew Koustenis, Gloria Patrick, Lorna Leonard, Rachel Grisham
Publikováno v:
Molecular Cancer Therapeutics. 20:P046-P046
Background: VS-6766 is a unique small molecule inhibitor that blocks MEK kinase activity and RAF phosphorylation of MEK. This mechanism of blockade has been shown to limit compensatory MEK activation, thereby potentially enhancing efficacy of MEK inh
Autor:
Rachel N. Grisham, Andrew Koustenis, Jonathan A. Pachter, Gloria Patrick, Nicoletta Colombo, Kathleen N. Moore, Robert L. Coleman, Bradley J. Monk, Michel Fabbro, Lorna Leonard, Susana Banerjee, Els Van Nieuwenhuysen, David M. O'Malley, Ana Oaknin
Publikováno v:
Journal of Clinical Oncology. 39:TPS5603-TPS5603
TPS5603 Background: VS-6766 is a unique small molecule inhibitor that blocks MEK kinase activity and RAF phosphorylation of MEK. This mechanism of blockade has been shown to limit compensatory MEK activation, thereby potentially enhancing efficacy of
Autor:
Stephanie Lustgarten, Alena Zalutskaya, Leo I. Gordon, Narayana I. Narasimhan, Hagop Youssoufian, Reem Karmali, K. M. Sprott, Gloria Patrick, David T. Weaver
Publikováno v:
Blood. 134:5251-5251
Background Duvelisib, an oral dual PI3K-δ and PI3K-γ inhibitor, is approved by the US Food and Drug Administration for the treatment of adult patients with relapsed or refractory (R/R) follicular lymphoma (FL) after ≥ 2 prior systemic therapies.
Publikováno v:
Annals of Clinical Psychiatry. 13:69-73
Autor:
Frederick A. Struve, John J. Straumanis, Mary-Jo Fitzgerald, John Leavitt, Gloria Patrick, Joseph E. Manno
Publikováno v:
Journal of Addictive Diseases. 19:71-87
Stringent exclusion criteria in drug abuse research are necessary to protect against methodological confounds compromising the interpretation of findings. However, reliance on self-report screening may fail to detect important exclusion variables. We