Page last updated: 2024-10-27

fexofenadine and Lung Neoplasms

fexofenadine has been researched along with Lung Neoplasms in 1 studies

fexofenadine: a second generation antihistamine; metabolite of the antihistaminic drug terfenadine; structure in first source; RN refers to HCl
fexofenadine : A piperidine-based anti-histamine compound.

Lung Neoplasms: Tumors or cancer of the LUNG.

Research Excerpts

ExcerptRelevanceReference
"Osimertinib is a potent, third-generation, irreversible, central nervous system active epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) that selectively inhibits EGFR-TKI sensitizing and EGFR T790M resistance mutations."2.90Modulation of Fexofenadine Pharmacokinetics by Osimertinib in Patients With Advanced EGFR-Mutated Non-Small Cell Lung Cancer. ( Calvo, E; deCastro Carpeno, J; Kim, SW; Laus, G; Lee, JS; Mann, H; Moreno, V; Vishwanathan, K; Weilert, D, 2019)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Calvo, E1
Lee, JS1
Kim, SW1
Moreno, V1
deCastro Carpeno, J1
Weilert, D1
Laus, G1
Mann, H1
Vishwanathan, K1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
An Open-label, Non-randomised, Phase I Study to Assess the Effect of Single and Multiple Oral Doses of Osimertinib (TAGRISSO™) on the Pharmacokinetics of a P-glycoprotein Probe Drug (Fexofenadine) in Patients With Advanced EGFRm NSCLC That Have Progressed[NCT02908750]Phase 124 participants (Actual)Interventional2017-03-02Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

1 trial available for fexofenadine and Lung Neoplasms

ArticleYear
Modulation of Fexofenadine Pharmacokinetics by Osimertinib in Patients With Advanced EGFR-Mutated Non-Small Cell Lung Cancer.
    Journal of clinical pharmacology, 2019, Volume: 59, Issue:8

    Topics: Acrylamides; Aged; Aniline Compounds; Anti-Allergic Agents; Antineoplastic Agents; ATP Binding Casse

2019