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Cleveland Clinic Brain Tumor and Neuro-Oncology Center Clinical ...

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<strong>Clevel<strong>and</strong></strong> <strong>Clinic</strong> <strong>Brain</strong> <strong>Tumor</strong> <strong>and</strong> <strong>Neuro</strong>-<strong>Oncology</strong> <strong>Center</strong>:Patient Data<br />

http://bti.ccf.org/cgi-bin/bti/auth/detailLAMINATE.cgi?id=613<br />

Page 4 of 4<br />

4/11/2013<br />

◦ platelets greater or equal to 100*10 9 cells/l<br />

◦ bilirubin < 1.5 times upper limit of laboratory normal<br />

◦ alkaline phosphatase, ASAT <strong>and</strong> ALAT < 2.5 times upper limit of laboratory normal<br />

◦ serum creatinine lower than 1.5 times upper limit of laboratory normal<br />

• All patients must use effective contraception if of reproductive potential. Females must not be pregnant or<br />

breast feeding<br />

• Absence of known HIV infection, chronic hepatitis B or hepatitis C infection<br />

• Absence of any other serious medical condition that could interfere with follow-up<br />

• Absence of any medical condition which could interfere with oral medication intake (e.g., frequent vomiting,<br />

partial bowel obstruction)<br />

• Absence of previous or concurrent malignancies at other sites with the exception of surgically cured<br />

carcinoma in situ of te cervix <strong>and</strong> non-melanoma skin cancer.<br />

• Absence of any psychological, familial, sociological or geographical condition potentially hampering<br />

compliance with the study protocol <strong>and</strong> follow-up schedule.<br />

• Before patient r<strong>and</strong>omization, written informed consent must be given according to ICH/GCP, <strong>and</strong><br />

national/local regulations.<br />

Patients can only be r<strong>and</strong>omized in this trial once.

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