Clinical Trials

Multiple Ascending Dose of BMS-911543

Location:

Rochester,  MN

Trial status:

Open for Enrollment

Why is this study being done?

The purpose of this first in human study is to determine if BMS-911543 is safe and tolerable in subjects with symptomatic intermediate-1, intermediate-2 or high risk myelofibrosis to permit clinical testing at the Maximum Tolerated Dose or at a Clinically Active Dose, and to determine if BMS-911543 will demonstrate efficacy in symptomatic myelofibrosis.

Who is eligible to participate?

Inclusion Criteria:

- Men and Women at least 18 years old

- A diagnosis of symptomatic, primary or secondary Myelofibrosis (MF) [World Health Organization (WHO) 2008 criteria] with intermediate-1, intermediate-2 or high risk disease as assessed using the Dynamic International Prognostic Scoring System international prognostic scoring system

- Last therapeutic or diagnostic treatment at least 28 days prior

- Any toxicity from prior therapies must have resolved to Grade ≤1

- Adequate Liver and Kidney Function

- Platelet count ≥50,000 cell mm³

- Absolute neutrophil count (ANC) ≥1,000 cells/mm3

- Hemoglobin ≥8.0 g/dL

Exclusion Criteria:

- Primary central nervous system tumors

- Subjects with currently active malignancy (other than MF) or with a prior history of malignancy with the exception of: (i) adequately treated basal cell carcinoma of the skin, (ii) curatively treated in situ carcinoma of the cervix, (iii) other malignancy that has undergone potentially curative therapy with no evidence of disease recurrence ≥3 years

- Any condition requiring chronic use of moderate/high dose steroids except inhalation or oral steroids for mild pulmonary disease

- Splenic irradiation ≤3 months prior to treatment with study drug

- Positive blood screen for hepatitis C antibody, hepatitis B surface antigen or Human Immunodeficiency Virus-1 (HIV-1), or HIV-2 antibodies

- Abnormalities in serum electrolytes

- Significant cardiovascular disease

- Current or recent gastrointestinal disease

- Evidence of uncontrolled active infection or active graft vs. host disease

- Inability to tolerate oral medication

Last updated: 06/18/2012

NCT ID:

NCT01236352