A Phase Ib/II, multicenter, open-label, dose escalation study of LGX818 in combination with MEK162 in adult patients with BRAF V600 - dependent advanced solid tumors

ovartis Farma S.p.A.0 个研究点目标入组 127 人开始时间: 2013年2月27日最近更新: 2014年7月14日

试验速览

暂无简介。

•Age = 18 years for both phases and arms
•Histologically confirmed diagnosis of locally advanced or metastatic melanoma (stage IIIB to IV per American Joint Committee on Cancer [AJCC]), or confirmed diagnosis of non-resectable advanced metastatic colorectal cancer (mCRC), or any other indication upon agreement with the Sponsor, whose disease has progressed despite previous antineoplastic therapy or for whom no further effective standard therapy is available.
•Written documentation of BRAF V600E mutation, or any other BRAF V600 mutation.
•Evidence of measurable disease as determined by RECIST v1.1.
•World Health Organization (WHO) Performance Status = 2.
•Negative serum pregnancy test within 72 hours prior to the first study
•dose in all women of childbearing potential.
•Other protocol-defined inclusion criteria may apply.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 114
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 13

•Progressive disease following prior treatment with RAF-inhibitors in combination with MEK-inhibitors.
•Symptomatic or untreated leptomeningeal disease.
•Symptomatic brain metastases. Patients are not permitted to receive enzyme inducing anti-epileptic drugs.
•Known acute or chronic pancreatitis.
•History or current evidence of retinal disease, retinal vein occlusion or ophthalmopathy.
•Clinically significant cardiac disease.
•Patients with abnormal laboratory values at Screening/baseline.
•Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of oral LGX818/MEK162
•Previous or concurrent malignancy.
•Pregnant or nursing (lactating) women.
•Other protocol-defined exclusion criteria may apply.

发起方

ovartis Farma S.p.A.