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Clinical Trials for Mesothelioma Patient Tumors—A Study to Find the Best Dose of SU011248: Study Criteria

Read about the study criteria for a current clinical trial about the use of SU011248 for patients with mesothelioma tumors. Please note: this information is provided by Weitz & Luxenberg for informational purposes only.

Arms and Interventions:

A: Experimental

Drug: Sunitinib, Pemetrexed, Cisplatin, Carboplatin

Dose finding study using Sunitinib daily by oral capsule in a continuous regimen or administered for 2 weeks out of every 3 weeks, with pemetrexed every 3 weeks or also with cisplatin 75 mg/m2 or carboplatin AUC=5 mg*min/mL until progression or unacceptable toxicity.

Inclusion Criteria:

  • Patients with a diagnosis of a solid cancer which is not responsive to standard therapy or for which no standard therapy exists.
  • Patient has a good performance status (ECOG 0 or 1).

Exclusion Criteria:

 

  • Prior treatment with either pemetrexed or SU011248.
  • Coughing up blood within 4 weeks before starting study treatment (small amounts okay).
  • Hypertension that cannot be controlled by medications.

Courtesy of ClinicalTrials.gov, a service of the U.S. National Institutes of Health

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Mesothelioma
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Clinical trials for mesothelioma
IN THIS SECTION
Measures for SU011248 in mesothelioma tumors
Criteria for study in mesothelioma tumors
Contact for SU011248 trial on mesothelioma

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see also:

Measures for SU011248 in mesothelioma tumors Outcome measures for study of SU011248 against mesothelioma tumors
Read about measures for use of SU011248 to treat mesothelioma tumors

Criteria for study in mesothelioma tumors Study criteria of mesothelioma tumors
Read study criteria for treatment of mesothelioma tumors

SU011248 for mesothelioma Clinical trial to study best SU011248 dose for mesothelioma patients
Read about a clinical study of SU011248 drug to treat mesothelioma