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Circulating Tumor Cells as a Window on Metastasis Biology in Lung Cancer
The American journal of pathology, 2011-03, Vol.178 (3), p.989-996
2011
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Dose escalation and expansion cohorts in patients with advanced breast cancer in a Phase I study of the CDK7-inhibitor samuraciclib
Nature communications, 2023-07, Vol.14 (1), p.4444-4444, Article 4444
2023
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Author Correction: Dose escalation and expansion cohorts in patients with advanced breast cancer in a Phase I study of the CDK7-inhibitor samuraciclib
Nature communications, 2023-08, Vol.14 (1), p.4741-4741, Article 4741
2023
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Ceralasertib (AZD6738), an Oral ATR Kinase Inhibitor, in Combination with Carboplatin in Patients with Advanced Solid Tumors: A Phase I Study
Clinical cancer research, 2021-10, Vol.27 (19), p.5213-5224
2021
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Effective delivery of Complex Innovative Design (CID) cancer trials-A consensus statement
British journal of cancer, 2020-02, Vol.122 (4), p.473-482
2020
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Abstract PS13-05: A phase 2 study of oral paclitaxel and encequidar (oPac+E) in the treatment of cutnaeous angiosarcoma: The breast angiosarcoma subgroup
Cancer research (Chicago, Ill.), 2021-02, Vol.81 (4_Supplement), p.PS13-05-PS13-05
2021
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A Phase I Trial of the Dual MET Kinase/OCT-2 Inhibitor OMO-1 in Metastatic Solid Malignancies Including MET Exon 14 Mutated Lung Cancer
The oncologist (Dayton, Ohio), 2023-12, Vol.28 (12), p.e1248-e1258
2023
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Abstract GS3-10: Study of samuraciclib (CT7001), a first-in-class, oral, selective inhibitor of CDK7, in combination with fulvestrant in patients with advanced hormone receptor positive HER2 negative breast cancer (HR+BC)
Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.GS3-10-GS3-10
2022
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Abstract P1-18-10: A clinical study of samuraciclib (CT7001), a first-in-class, oral, selective inhibitor of CDK7, in patients with advanced triple negative breast cancer (TNBC)
Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P1-P1-18-10
2022
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Abstract 4791: OMO-1, a potent, highly selective, orally bioavailable, MET kinase inhibitor with a favorable preclinical toxicity profile, shows both monotherapy activity, against MET pathway-driven tumors, and EGFR TKI combination activity in acquired resistance models
Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4791-4791
2018
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Analytical Validation of BRAF Mutation Testing from Circulating Free DNA Using the Amplification Refractory Mutation Testing System
The Journal of molecular diagnostics : JMD, 2014-05, Vol.16 (3), p.343-349
2014
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Continual reassessment method for dose escalation clinical trials in oncology: a comparison of prior skeleton approaches using AZD3514 data
BMC cancer, 2016-08, Vol.16 (1), p.703-703, Article 703
2016
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Effects of third generation aromatase inhibitors on bone health and other safety parameters: Results of an open, randomised, multi-centre study of letrozole, exemestane and anastrozole in healthy postmenopausal women
European journal of cancer (1990), 2007-11, Vol.43 (17), p.2523-2531
2007
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Effects of Src kinase inhibition by saracatinib (AZD0530) on bone turnover in advanced malignancy in a Phase I study
Bone (New York, N.Y.), 2012-04, Vol.50 (4), p.885-892
2012
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Translational modelling of preclinical cardiovascular findings to patients
Journal of pharmacological and toxicological methods, 2014-11, Vol.70 (3), p.326-327
2014
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Tissue collection in drug discovery and development research
European journal of cancer supplements, 2007-12, Vol.5 (9), p.33-36
2007
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