Abstract Lessons Learned. A phase I study of the pan‐class I phosphoinositide 3‐kinase inhibitor pilaralisib (in capsule formulation) in advanced solid tumors established the maximum tolerated dose as 600 mg once daily.The current study investigated pilaralisib in tablet formulation.Pilaralisib tablets were associated with a favorable safety profile and preliminary antitumor activity.Based on pharmacokinetic data, the recommended phase II dose of pilaralisib tablets was established as 400 mg once daily. Background. A phase I trial of pilaralisib, an oral pan‐class I phosphoinositide 3‐kinase (PI3K) inhibitor, established the maximum tolerated dose (MTD) of the capsule formulation in patients with advanced solid tumors as 600 mg once daily. ...
Background: The PI3K/protein kinase B (AKT) pathway is commonly activated in several tumor types. Se...
Advanced Solid Tumors; PI3K beta/delta inhibitorTumores sólidos avanzados; Inhibidor de PI3K beta/de...
We report the results from a phase I study of buparlisib, an oral pan-class I phosphotidyinositol-3-...
Pilaralisib (SAR245408), a pan-class I PI3K inhibitor, has been investigated in Phase I/II trials in...
PurposeWe report the first-in-human phase Ia study to our knowledge (ClinicalTrials.gov identifier: ...
Phosphatidylinositol 3-kinase (PI3K) pathway activation is associated with resistance to paclitaxel ...
PURPOSE: This first-in-human dose-escalation trial evaluated the safety, tolerability, maximal-toler...
PURPOSE: This first-in-human dose-escalation trial evaluated the safety, tolerability, maximal-toler...
GSK2126458 (GSK458) is a potent inhibitor of PI3K (α, β, γ, and δ), with preclinical studies demonst...
Purpose: To evaluate the safety, MTD, pharmacokinetics, pharmacodynamics, and preliminary antitumor ...
textabstractPurpose: This first-in-human phase I trial assessed the safety, tolerability, and prelim...
This phase I study aimed to determine tolerability and preliminary efficacy of single-agent alpelisi...
Ajuts: This study was sponsored by Pfizer Inc.This phase I, four-arm, open-label study (NCT01347866)...
Purpose: This phase I dose-escalation study investigated the maximum-tolerated dose (MTD), dose-limi...
Aim: The phosphatidylinositol 3-kinase (PI3K) pathway is a potential therapeutic target in non-small...
Background: The PI3K/protein kinase B (AKT) pathway is commonly activated in several tumor types. Se...
Advanced Solid Tumors; PI3K beta/delta inhibitorTumores sólidos avanzados; Inhibidor de PI3K beta/de...
We report the results from a phase I study of buparlisib, an oral pan-class I phosphotidyinositol-3-...
Pilaralisib (SAR245408), a pan-class I PI3K inhibitor, has been investigated in Phase I/II trials in...
PurposeWe report the first-in-human phase Ia study to our knowledge (ClinicalTrials.gov identifier: ...
Phosphatidylinositol 3-kinase (PI3K) pathway activation is associated with resistance to paclitaxel ...
PURPOSE: This first-in-human dose-escalation trial evaluated the safety, tolerability, maximal-toler...
PURPOSE: This first-in-human dose-escalation trial evaluated the safety, tolerability, maximal-toler...
GSK2126458 (GSK458) is a potent inhibitor of PI3K (α, β, γ, and δ), with preclinical studies demonst...
Purpose: To evaluate the safety, MTD, pharmacokinetics, pharmacodynamics, and preliminary antitumor ...
textabstractPurpose: This first-in-human phase I trial assessed the safety, tolerability, and prelim...
This phase I study aimed to determine tolerability and preliminary efficacy of single-agent alpelisi...
Ajuts: This study was sponsored by Pfizer Inc.This phase I, four-arm, open-label study (NCT01347866)...
Purpose: This phase I dose-escalation study investigated the maximum-tolerated dose (MTD), dose-limi...
Aim: The phosphatidylinositol 3-kinase (PI3K) pathway is a potential therapeutic target in non-small...
Background: The PI3K/protein kinase B (AKT) pathway is commonly activated in several tumor types. Se...
Advanced Solid Tumors; PI3K beta/delta inhibitorTumores sólidos avanzados; Inhibidor de PI3K beta/de...
We report the results from a phase I study of buparlisib, an oral pan-class I phosphotidyinositol-3-...