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  1. No Access

    Article

    The pH-altering agent omeprazole affects rate but not the extent of ibrutinib exposure

    This drug-interaction study evaluated the effect of omeprazole, a proton-pump inhibitor, on ibrutinib’s pharmacokinetics (PK) in healthy participants.

    Jan de Jong, Nahor Haddish-Berhane, Peter Hellemans in Cancer Chemotherapy and Pharmacology (2018)

  2. Article

    Correction to: Ibrutinib does not prolong the corrected QT interval in healthy subjects: results from a thorough QT study

    The author would like to correct the affiliations and conflict of interest in the publication of the original article. The corrected details are given below for your reading.

    Jan de Jong, Peter Hellemans, James Juhui Jiao in Cancer Chemotherapy and Pharmacology (2018)

  3. No Access

    Article

    Ibrutinib does not prolong the corrected QT interval in healthy subjects: results from a thorough QT study

    Ibrutinib is an orally administered, irreversible Bruton’s tyrosine kinase inhibitor for treatment of B-cell malignancy. This study evaluated the effects of single-dose ibrutinib at therapeutic and supratherap...

    Jan de Jong, Peter Hellemans, James Juhui Jiao in Cancer Chemotherapy and Pharmacology (2017)

  4. Article

    Open Access

    The effect of food on the pharmacokinetics of oral ibrutinib in healthy participants and patients with chronic lymphocytic leukemia

    To assess ibrutinib pharmacokinetics under fasted and fed conditions, impact of food-intake timing, and the safety and tolerability.

    Jan de Jong, Juthamas Sukbuntherng, Donna Skee in Cancer Chemotherapy and Pharmacology (2015)

  5. No Access

    Article

    Population pharmacokinetic model of ibrutinib, a Bruton tyrosine kinase inhibitor, in patients with B cell malignancies

    Ibrutinib is an oral Bruton’s tyrosine kinase inhibitor, recently approved for the treatment of mantle cell lymphoma (MCL) and chronic lymphocytic leukemia (CLL) patients with at least one prior therapy. We d...

    Eleonora Marostica, Juthamas Sukbuntherng in Cancer Chemotherapy and Pharmacology (2015)

  6. No Access

    Article

    Single- and multiple-dose disposition kinetics of sunitinib malate, a multitargeted receptor tyrosine kinase inhibitor: comparative plasma kinetics in non-clinical species

    The purpose of these extensive non-clinical studies was to assess pharmacokinetics and dispositional properties of sunitinib and its primary active metabolite (SU12662).

    Joshua Ö. Haznedar, Shem Patyna, Carlo L. Bello in Cancer Chemotherapy and Pharmacology (2009)