Richard Baldry

ORCID: 0000-0003-0525-1119
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About
Contact & Profiles
Research Areas
  • Brain Metastases and Treatment
  • Lung Cancer Treatments and Mutations
  • Pregnancy and Medication Impact
  • Cancer Genomics and Diagnostics
  • Pulmonary Hypertension Research and Treatments
  • Dialysis and Renal Disease Management
  • HER2/EGFR in Cancer Research
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Lung Cancer Research Studies
  • Renal Diseases and Glomerulopathies

AstraZeneca (United Kingdom)
2024

Leptomeningeal metastases (LMs) exhibit a high incidence in patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) post-treatment first- or second-generation EGFR tyrosine kinase inhibitors (TKIs). This investigation evaluates the efficacy, safety, and pharmacokinetics of 80 mg once daily osimertinib LMs resistant to prior TKIs.

10.1200/jco.24.00708 article EN Journal of Clinical Oncology 2024-06-03

The endothelin A receptor antagonist zibotentan, combined with the sodium‐glucose co‐transporter‐2 inhibitor dapagliflozin, is being investigated for treatment of chronic kidney disease high proteinuria. To allow women childbearing potential access to this treatment, highly effective contraception required and drug interactions compromising reliability must be avoided. This study risk pharmacokinetic (PK) interaction between zibotentan contraceptives ethinyl estradiol levonorgestrel....

10.1002/cpt.3280 article EN cc-by-nc-nd Clinical Pharmacology & Therapeutics 2024-04-30

8582 Background: Leptomeningeal metastases (LM) present with a high incidence in EGFR-mutated NSCLC following treatment first- or second-generation EGFR TKIs. Osimertinib has demonstrated significant clinical efficacy LM at double dose (160mg), attributed to its superior blood-brain barrier penetration. This study aims delineate the efficacy, safety, and pharmacokinetic profile of 80mg osimertinib for patients exhibiting resistance earlier-generation Methods: The BLOSSOM trial is Phase II,...

10.1200/jco.2024.42.16_suppl.8582 article EN Journal of Clinical Oncology 2024-06-01
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