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A Study of R1507 in Combination With Multiple Standard Chemotherapy Treatments in Patients With Advanced Solid Tumors

Registration Number
NCT00811993
Lead Sponsor
Hoffmann-La Roche
Brief Summary

This study will evaluate the safety and tolerability of R1507 in combination with 12 distinct standard chemotherapy drug regimens and an additional R1507 monotherapy arm in patients with advanced malignant neoplasms.The 12 regimens will be tested in parallel. There are 3 subsets of patients who are eligible for the study: untreated, treated and requiring further treatment, or treated and failed and for whom adding R1507 represents a suitable treatment for their disease. All regimens will first test doses of R1507 which are less than the maximally administered dose, and if tolerated, the dose will be escalated in subsequent patients. The anticipated time on study treatment is until disease progression, and the target sample size is 100-500 individuals.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
104
Inclusion Criteria
  • adult patients, >=18 years of age;
  • malignant neoplasms;
  • failed prior standard curative therapy;
  • ECOG performance Status of 0 or 1;
  • adequate bone marrow, hepatic and renal function;
  • life expectancy greater than 8 weeks.
Exclusion Criteria
  • chemotherapy within 2 weeks of start of therapy;
  • prior irradiation within 4 weeks prior to start of therapy;
  • prior treatment with agents targeting IGF-IR inhibition, or other investigational agents;
  • major surgery or significant traumatic injury within 2 weeks prior to study start;
  • patients receiving concurrent antibody or immunotherapy;
  • other exclusion criteria are related to specific treatment regimens.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
2paclitaxel-
1RG1507-
1erlotinib [Tarceva]-
10RG1507-
11RG1507-
11bevacizumab [Avastin]-
12RG1507-
12pemetrexel-
13RO1507-
2RG1507-
2bevacizumab [Avastin]-
3RG1507-
3carboplatin-
3etoposide-
4bevacizumab [Avastin]-
4mFOLFOX6-
5RG1507-
8RG1507-
5capecitabine [Xeloda]-
5trastuzumab [Herceptin]-
6sorafenib-
7RG1507-
7erlotinib [Tarceva]-
9RG1507-
9bevacizumab [Avastin]-
7bevacizumab [Avastin]-
4RG1507-
6RG1507-
11docetaxel-
1gemcitabine-
10temozolomide-
8irinotecan-
8cetuximab-
9carboplatin-
9paclitaxel-
Primary Outcome Measures
NameTimeMethod
Adverse events, laboratory parameters, vital signsThroughout study
Secondary Outcome Measures
NameTimeMethod
Trough levels of R1507Throughout study
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