A Study of RO5045337 in Combination With Doxorubicin in Patients With Soft Tissue Sarcoma
| Status: | Completed |
|---|---|
| Conditions: | Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 8/3/2016 |
| Start Date: | May 2012 |
| End Date: | June 2013 |
A Multi-center, Open-label Phase IB Study of Escalating Doses of RO5045337, an Oral Small Molecule MDM2 Antagonist, in Combination With Doxorubicin in Patients With Soft Tissue Sarcoma
This multicenter, open-label, Phase 1b study will evaluate the safety, pharmacokinetics and
efficacy of RO5045337 in combination with doxorubicin in patients with soft tissue sarcoma.
Cohorts of patients will receive escalating doses of RO5045337 orally on Days 1-5 (1-3) of
each 28-day cycle in combination with doxorubicin 60 mg/m2 intravenously on Day 1 of each
cycle for up to 6 cycles.
efficacy of RO5045337 in combination with doxorubicin in patients with soft tissue sarcoma.
Cohorts of patients will receive escalating doses of RO5045337 orally on Days 1-5 (1-3) of
each 28-day cycle in combination with doxorubicin 60 mg/m2 intravenously on Day 1 of each
cycle for up to 6 cycles.
Inclusion Criteria:
- Adult patients, >/= 18 years of age
- Histologically or cytologically confirmed soft tissue sarcoma
- Evaluable disease according to RECIST version 1.1 criteria
- Eastern Cooperative Oncology Group (ECOG) performance status 0 to 1
- Eligible for doxorubicin therapy
- Acute toxicities from prior anti-tumor therapy, surgery or radiotherapy must have
resolved to NCI-CTCAE Grade
- Adequate bone marrow, hepatic and renal function
- Patients with stable CNS metastases are eligible
Exclusion Criteria:
- Previous treatment with limiting doses of doxorubicin
- Patients receiving any other investigational or commercial agents or therapies
administered with the intention to treat their malignancy or other ailment days from Day 1 dosing on study treatment
- History of seizure disorders or unstable CNS metastases
- Severe and/or uncontrolled medical conditions or other conditions that could affect
the participation in the study
- Pregnant or breastfeeding women
- HIV positive patients who are currently receiving combination anti-retroviral therapy
- Patients with known coagulopathy, platelet disorder or history of non-drug induced
thrombocytopenia
- Patients receiving oral or parenteral anti-coagulants/anti-platelet agents
We found this trial at
6
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