ASA404 in Combination With Carboplatin/Paclitaxel/Cetuximab in Treating Patients With Refractory Solid Tumors

Withdrawn before enrolling · Phase 1

Conditions studied: Tumors

In brief

This phase I trial is studying the side effects and best dose of an investigational drug called DMXAA (5-6-dimethylxanthenone-4-acetic acid) or ASA404 when given together with carboplatin, paclitaxel and cetuximab to treat patients with refractory solid tumors.

Key facts

Study ID

NCT01031212

Run by

University of California, San Francisco

People needed

0

Starts

2010-01-01

Expected to finish

2013-06-01

Last updated by the study team

2013-05-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histological confirmed malignancy of advanced, incurable solid tumor
• Progression following standard therapy, or no acceptable standard treatment options, or eligible if standard therapy consists of a platinum-based doublet
• Measurable or evaluable disease. Measurable disease required for enrollment in dose expansion cohort at MTD
• ECOG 0-2
• Baseline neuropathy grade ≤ 1
• leukocytes >3,000/mcL
• absolute neutrophil count >1,500/mcL
• platelets >100,000/mcL
• total bilirubin within normal institutional limits
• AST(SGOT)/ALT(SGPT) <1.5 X institutional ULN
• creatinine within 1.5 x normal institutional limits OR creatinine clearance >60 mL/min/1.73 m2
• Ability to give written informed consent and willingness to comply with requirements of the protocol
• Women of child-bearing potential must have a negative pregnancy test within 14 days of beginning study drug and agree to use an effective method of birth control during treatment and for six months after last dose of study drug
• Male patients whose sexual partners are women of reproductive potential must be surgically sterile or agree to use a double method of contraception during the study and for six months after last dose of study drug. One of method must be a condom
• Patients with known brain metastases should have "stable disease" defined as no growth over a 6 week period after definitive therapy (surgical or RT), and off steroids and anticonvulsive therapy

You may not qualify if…

• Chemotherapy, hormonal therapy or biologic therapy within 3 weeks (6 weeks for nitrosoureas or mitomycin C) prior to the start of study therapy or not recovered to < grade 2 from adverse events due to prior agents
• Prior therapy with EGFR inhibitors is permitted
• Patients receiving palliative radiation therapy <2 weeks earlier. Patients must have recovered from all toxicities of radiation
• Receiving any other investigational agents
• Any severe and/or uncontrolled intercurrent medical conditions or other conditions that could affect participation in the study
• Any of the following cardiac abnormalities: unstable angina pectoris, including Prinzmetal variant angina, New York Heart Association (NYHA) Classification for Congestive Heart Failure Grade III or greater, myocardial infarction or stroke ≤ 12 months prior to study treatment, long QT syndrome, baseline 12 lead ECG QTc of >450msec per central evaluation, history of sustained ventricular tachycardia, history of ventricular fibrillation or Torsades de Pointes, right bundle branch block and left anterior hemiblock (bifascicular block), bradycardia (<50 beats per minute)
• Concomitant use of drugs with a risk of causing Torsades de Pointes
• PT/PTT > 1.5 x ULN
• Receiving full-dose anticoagulation (low-dose warfarin for a central line allowed)
• History of another primary malignancy less than 5 years prior, except non-melanoma skin cancer or cervical cancer in-situ
• Major surgery ≤ 4 weeks prior (requiring general anesthesia or respiratory assistance)(endoscopic exams with diagnostic intent allowed)
• Minor surgery ≤ 2 weeks prior (not requiring general anesthesia or respiratory assistance)
• Insertion of vascular access device allowed
• Not recovered from surgery-related complications
• Systolic BP >160mmHg and/or diastolic BP >90mmHg while on medication for hypertension
• Hemoptysis associated with chest malignancy <4 weeks (>1 teaspoon)
• History of hypersensitivity reactions to TAXOL or other drugs formulated in Cremophor® EL (polyoxyethylated castor oil)
• History of severe allergic reactions to cisplatin or other platinum-containing compounds
• History of acute hemorrhagic events requiring hospital admission or blood transfusion
• Pregnant or lactating women
• Fertile women and men not willing to comply with birth control instructions
• Any condition that compromises compliance with objectives and procedures of this protocol, as judged by the principal investigator

Where it is running

• UCSF Helen Diller Family Comprehensive Cancer Center — San Francisco, California, United States

Full record on ClinicalTrials.gov

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