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imotuzumab in tumors of head and neck .Phase IV

Phase 4
Recruiting
Conditions
Tumors of head and neck in advanced stages.
Registration Number
RPCEC00000145
Lead Sponsor
Center of Molecular Immunology (CIM)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
404
Inclusion Criteria

1.Patient that expresses the voluntary written into the studio with the signing of the informed consent. 2.Patient with age equal or greater than 18 years. 3.Expectation of life equal to or greater than 6 months. 4.Clinical status according to criteria of the ECOG less than or equal to 3. 5.Laboratory parameters(considering type of processing and equipment used): Hematopoietic - hemoglobin (Hb) greater than or equal to 100g/L hematocrit 0.30-0.40 in women and 0.30-0.44 in men, count of leukocytes ? 3000/?L = 3 x 109 L, CAN ? 1500/?L = 1.5 x 109 /L, platelets count greater than or equal to 100000/?L = 100 x 109 L, biochemical-liver: ALAT (TGP), ASAT (TGO), alkaline phosphatase, up to 2.5 times upper limit of normal for each clinical site; LDH and albumin normal value; Kidney: serum creatinine normal value.

Exclusion Criteria

1.Pregnancy, postpartum or breastfeeding. 2.Chronic disease associated in stage of decompensation (example: heart disease, diabetes mellitus, arterial hypertension). 3.Brain metastasis, diagnosed by TAC, not controlled or in progression. 4.Presence of a second primary tumor, with the exception of basal carcinomasor squamous skin and carcinoma in situ treated neck. 5.Patient who is receiving another investigational medicinal product at the time of inclusion. 6.Treatment with nimotuzumab in the 6 months prior to the time of inclusion. 7.Prior knowledge of allergy or sensitivity to the nimotuzumab or any component of the formulation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serious EA with causal relationship with nimotuzumab (definitive, very likely or probable).Measuring time:24 months
Secondary Outcome Measures
NameTimeMethod
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