Overview

AS703569 and Gemcitabine Combination in Advanced Malignancies

Status:
Completed
Trial end date:
2011-02-01
Target enrollment:
0
Participant gender:
All
Summary
In clinical practice and research, combination of anticancer agents is often used to improve efficacy of treatment. In vitro and in vivo experiments have shown additive-synergistic anti-tumour effects of AS703569 treatment when combined with gemcitabine. Specifically, additive-synergistic anti-tumour effects were noticed when the two agents were given sequentially and not concomitantly i.e. AS703569 given the day before or the day after gemcitabine. This trial was designed to investigate in parallel two regimens testing sequential administration of AS703569 either the day after gemcitabine infusion, (Regimen 1) or the day before (Regimen 2).
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Merck KGaA
Merck KGaA, Darmstadt, Germany
Treatments:
Gemcitabine
Criteria
Inclusion Criteria:

Histologically/cytologically confirmed diagnosis of measurable or assessable malignancy,
who meets one of the following conditions:

Subject with a tumour for which gemcitabine is approved, Subject with a tumour for which
gemcitabine is considered standard of care, Subject with other tumour type either
refractory or intolerant to or for whom there is not an accepted standard treatment.

Male or female with at least 18 years of age. Life expectancy of at least 3 months.

Eastern Cooperative Oncology Group (ECOG) Performance Status < 2.

No more than 3 prior chemotherapy regimens for advanced/metastatic disease.

At least 4 weeks since last chemotherapy, hormonal therapy, immunotherapy, biological or
any other pharmacological or investigational treatment or radiotherapy (6 weeks wash-out
for nitrosoureas and mitomycin C, 5 half-lives for non-cytotoxics). Subjects on chronic
hormonal therapy may continue with the same treatment unchanged.

Adequate renal, hepatic and bone marrow functions (assessed 7 days before inclusion in the
trial) as defined by:

Serum creatinine