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threonine/sarcoma

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This is a first-in-human, Phase 1a/1b (dose escalation and expansion) study of BGB-3245 in participants with tumors harboring B-RAF mutations that are likely to respond to a RAF dimer inhibitor. BGB-3245 is a second-generation B-RAF inhibitor that has demonstrated potent inhibitory activity against
Inclusion criteria: 1. Female or male, 18 years of age or older; 2. Histologically or cytologically proven diagnosis of NSCLC; 3. Able to get tumor tissue gene testing results by lung cancer Polymerase Chain Reaction(PCR)panel kit carried out in hospital 4. Signed and dated informed

9-ING-41 in Patients With Advanced Cancers

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9-ING-41 is a first-in-class, intravenously administered, maleimide-based small molecule potent selective GSK-3β inhibitor with significant pre-clinical antitumor activity. GSK-3 is a serine/threonine kinase initially described as a key regulator of metabolism and has a role in diverse disease
PRIMARY OBJECTIVES: I. Determine the progression‐free survival in patients with newly diagnosed metastatic colorectal cancer treated with modified fluorouracil, leucovorin calcium, and oxaliplatin 6 (mFOLFOX6)/bevacizumab and PRI‐724 vs. mFOLFOX6/bevacizumab alone. SECONDARY OBJECTIVES: I. Overall

Gemcitabine Plus Rapamycin Versus Gemcitabine to Treat Advanced Soft Tissue Sarcoma

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Phase I Study of DOXIL and Temsirolimus in Resistant Solid Malignancies

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Phase I Study of Docetaxel and Temsirolimus in Resistant Solid Malignancies

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