MK-4827 in BRCA Ovarian Cancer and Other Advanced Solid Tumours
Research type
Research Study
Full title
A Phase Ia Study of MK-4827 in Patients With Advanced Solid Tumors and Phase Ib Study in Patients with BRCA Mutant Ovarian Cancer
Sponsor organisation
Merck & Co
Eudract number
2008-000054-12
ISRCTN Number
N/A
Clinicaltrials.gov Identifier
N/A
Research summary
This study of the novelanti-cancer agent, MK-4827, is designed to identify a dose level suitable forfurther investigation and development. It is divided into two phases. In the first phase, the doses of MK-4827 areincreased and the tolerability to each dose level determined. Once a safe doseof MK-4827 is identified, the number of patients studied at that dose level isincreased to confirm the suitability of the dose. Once a suitable dose forfurther investigation is identified in the first phase of the study, theefficacy of MK-4827 will be studied in a small number of patients who areconsidered to be most likely to benefit from this treatment.
REC name
London - Chelsea Research Ethics Committee
REC reference
08/H0801/98
Date of REC Opinion
29 Oct 2008
REC opinion
Further Information Favourable Opinion