Combined autophagy and HDAC inhibition: a phase I safety, tolerability, pharmacokinetic, and pharmacodynamic analysis of hydroxychloroquine in combination with the HDAC inhibitor vorinostat in patients
with advanced solid tumors.
The Maharaj Institute has an FDA IND clinical trial protocol (08001 - BMSCTI) for investigating a novel cancer therapy using transfusions of white blood cells from healthy donors to patient
with advanced solid tumors.
Data from a phase II study of cabozantinib (XL184) in patients
with advanced solid tumors show that the drug has activity in both bone and soft tissue.
Of the 22 patients whose tumors successfully grafted, six died before data from the mice were available, but in 13 of the remaining 16 cases, there was a positive correlation between mouse and human results.2 In a second study, performed in collaboration with Manuel Hidalgo of the Spanish National Cancer Research Center, the team found that 6 of 13 patients
with advanced solid tumors who were treated based on results from personalized PDX mice had partial tumor remissions, even in cases where genetic sequencing of the tumor showed no actionable mutations.3
Phase I Clinical Trial of VX - 970 in Combination with the Topoisomerase I Inhibitor Irinotecan in Patients
with Advanced Solid Tumors
A phase I clinical trial conducted by investigators at the University of Texas San Antonio, showed that the combination of HCQ and the chemotherapy drug vorinostat in 27 patients
with advanced solid tumors, including renal cell carcinoma and colon cancer, was clinically safe and inhibited autophagy.
Trial # 2: Phase I trial of HCQ with dose - intense temozolomide in patients
with advanced solid tumors and melanoma
The Phase I clinical trial of OMP - 54F28 (FZD8 - Fc) is an open - label dose escalation study in patients
with advanced solid tumors for which there was no remaining standard curative therapy.
Not exact matches
«We look forward to conducting further research through the STARTRK - 2 phase II trial and are hopeful that treatment
with entrectinib in patients
with a range of
advanced or metastatic
solid tumors harboring NTRK1 / 2/3, ROS1, or ALK gene fusions will result in very meaningful benefit.»
Dent is collaborating
with Massey clinical researchers to propose a study investigating the effectiveness of the combination of neratinib, sorafenib and pemetrexed in all
advanced solid tumors.
Another key finding was observing the inhibitor effect on
tumor models
with a gene PTEN deficiency as a biomarker — of huge interest because PTEN, a
tumor suppressor, is known to be defective in as many as half of all
advanced solid tumor cancers.
Locally
advanced pancreatic cancer has the lowest survival rate of any
solid tumor,
with a cumulative five - year survival rate of only 4 percent for all stages of disease.
A Phase II Study of the PARP Inhibitor Olaparib (AZD2281) Alone and in Combination
with AZD1775, AZD5363, or AZD2014 in
Advanced Solid Tumors - OLAPCO (OLAParib COmbinations)
A Phase 1 / 2a Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of PLX8394 in Patients
with Advanced, Unresectable
Solid Tumors
My Pathway: An Open - Label Phase IIA Study Evaluating Trastuzumab / Pertuzumab, Erlotinib, Vemurafenib / Cobimetinib, Vismodegib, Alectinib, and Atezolizumab in Patients Who Have
Advanced Solid Tumors with Mutations or Gene Expression Abnormalities Predictive of Response to One of These Agents
A Phase I / II Study of Pembrolizumab (MK - 3475) in Children
with Advanced Melanoma or a PD - L1 Positive
Advanced, Relapsed or Refractory
Solid Tumor or Lymphoma