Překonávají klinické studie fáze 0 stagnující vývoj protinádorových léčiv?
Překonávají klinické studie fáze 0 stagnující vývoj protinádorových léčiv?
Recent guidance from the US Food and Drug Administration supports the conduct of a new type of exploratory clinical trials, commonly called phase 0 clinical trials, on the development of innovative anticancer agents, particularly targeted agents. Phase 0 clinical trials are controversial mainly because of the lack of clinical benefit to the participant patients. However, it was recognized that Phase 0 clinical trials can provide a platform to assessing the biological effects on the targets in tumoral human samples, evaluate biomarkers for drug effects and to generate essential human pharmacokinetics and pharmacodynamics data earlier in the drug development. It is expected that such trials will became a routine part of early-phase oncological drug development in the future.
Key words:
phase 0 clinical trials – targeted therapy – cancer
Autoři:
L. Mendoza
Působiště autorů:
INC Research, Prague, Czech Republic
Vyšlo v časopise:
Klin Onkol 2011; 24(2): 143-145
Kategorie:
Stručné sdělení
Souhrn
Recent guidance from the US Food and Drug Administration supports the conduct of a new type of exploratory clinical trials, commonly called phase 0 clinical trials, on the development of innovative anticancer agents, particularly targeted agents. Phase 0 clinical trials are controversial mainly because of the lack of clinical benefit to the participant patients. However, it was recognized that Phase 0 clinical trials can provide a platform to assessing the biological effects on the targets in tumoral human samples, evaluate biomarkers for drug effects and to generate essential human pharmacokinetics and pharmacodynamics data earlier in the drug development. It is expected that such trials will became a routine part of early-phase oncological drug development in the future.
Key words:
phase 0 clinical trials – targeted therapy – cancer
Zdroje
1. Twombly R. Slow start to phase 0 as researchers debate value. J Natl Cancer Inst 2006; 98(12): 804–806.
2. Guidance for industry, investigators, and reviewers. Exploratory IND studies. U.S. department of health and human services. Food and drug administration. Center for drug evaluation and research (CDER). January 2006.
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4. Kinders R, Parchment RE, Ji J et al. Phase 0 clinical trials in cancer drug development: from FDA guidance to clinical practice. Mol Interv 2007; 7(6): 325–334.
5. European Medicines Agency, Committee for medicinal products for human use. Position paper on non-clinical safety studies to support clinical trials with a single microdose. London, June 23, 2004.
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7. Kummar S, Kinders R, Rubinstein L et al. Compressing drug development timelines in oncology using phase “0” trials. Nat Rev Cancer 2007; 7(2): 131–139.
8. Johnson JI, Decker S, Zaharevitz D et al. Relationships between drug activity in NCI preclinical in vitro and in vivo models and early clinical trials. Br J Cancer 2001; 84(10): 1424–1431
9. Von Hoff DD, Turner J. Response rates, duration of response, and dose response effects in phase I studies of antineoplastics. Invest New Drugs 1991; 9(1): 115–122.
10. Abdoler E, Taylor H, Wendler D. The ethics of phase 0 oncology trials. Clin Cancer Res 2008; 14(12): 3692–3697.
11. Pocard M, Soria JC, Aldaz-Carroll L et al. Phase 0 clinical trials in oncology: an exploratory methodology for constructing a study with patients undergoing surgery for metastatic disease. J Clin Oncol 2010; 28(30): 4551–4553.
12. Kummar S, Kinders R, Gutierrez ME et al. Phase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies. J Clin Oncol 2009; 27(16): 2705–2711.
Štítky
Detská onkológia Chirurgia všeobecná OnkológiaČlánok vyšiel v časopise
Klinická onkologie
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