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Antineoplastic Agents clinical trials

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NCT ID: NCT02484833 Completed - Clinical trials for Antineoplastic Agents

Erbitux MEtastatic Colorectal Cancer Strategy Study

Start date: February 2015
Phase: Phase 3
Study type: Interventional

- To investigate whether cetuximab alone (given until progression or cumulative toxicity) after 8 cycles of FOLFIRI + cetuximab results in a non inferior Progression Free Survival when compared with continuous FOLFIRI + cetuximab (given until progression or cumulative toxicity). - To assess whether an improvement in the incidence of grade 3-4 hematological and non-hematological adverse events (AEs) can be achieved in the experimental arm (cetuximab alone after 8 cycles FOLFIRI + cetuximab) as compared to the continuous chemotherapy arm (FOLFIRI plus cetuximab) - To explore the possibility of using liquid biopsies for molecular profiling as well as monitoring treatment activity in mCRC pts receiving cetuximab based therapy

NCT ID: NCT02468245 Active, not recruiting - Clinical trials for Antineoplastic Agents

Does a Nursing Intervention Improve Adherence to Oral Chemotherapies in the Outpatient Cancer Treatment Setting?

Start date: January 2015
Phase: N/A
Study type: Interventional

This study is being conducted by Bassett Healthcare Network in coordination with Bassett Cancer Institute. Patients prescribed oral chemotherapies will be approached to consider consent to this study. This study will try to establish if nursing interventions can help improve patients' adherence to taking their oral chemotherapies as prescribed by their doctor. Oral chemotherapies are emerging as a growing treatment of choice for many cancer diagnoses. Adherence to the prescribed treatment plan is very important to gain the best response to these types of treatments. The study will examine if nursing intervention via weekly phone calls may help improve adherence to oral chemotherapy treatment plans.

NCT ID: NCT01991691 Completed - Clinical trials for Antineoplastic Agents

Tablet-based Patient Reported Outcome

Start date: September 2013
Phase: N/A
Study type: Interventional

This study is a single arm feasibility study. Patients that have been diagnosed with carcinoma and are undergoing chemotherapy have to document chemotherapy associated side effects on a regular basis by means of a tablet-based online questionnaire. Goal of the study is to find out if patients that are undergoing chemotherapy are willing to document chemotherapy associated side effects by means of a tablet-based online questionnaire.

NCT ID: NCT01316458 Completed - Prostatic Neoplasm Clinical Trials

Glivec in Prostate Cancer Patients With Rising PSA Following Radical Prostectomy

Start date: June 2003
Phase: Phase 2
Study type: Interventional

To investigate the ability of 600 mg of Glivec®, given once daily by mouth to patients with rising PSA following radical prostatectomy, to produce a sustained biochemical response during the first 6 months of treatment.

NCT ID: NCT01169792 Completed - Breast Neoplasms Clinical Trials

Study of Cytochrome P450 Polymorphisms (CYP2D6, CYP3A4/5 and CYP2C19) in Breast Cancer Patients

Start date: n/a
Phase: N/A
Study type: Observational

The genetic polymorphisms of the cytochrome P450 may influence on the metabolism of tamoxifen. The investigators want to - evaluate the frequency or incidence of the genetic polymorphisms of cytochrome P450 subfamilies(CYP2D6, CYP3A4/5 and CYP2C19) in breast cancer patients, and - analyze the association between the genetic polymorphisms of cytochrome P450 subfamilies and clinical outcomes in breast cancer patients treated by adjuvant tamoxifen therapy.

NCT ID: NCT00541801 Completed - Clinical trials for Heart Failure, Congestive

Acoustic Cardiographic Assessment of Heart Function in Comparison to Doppler-echocardiography

Start date: March 2007
Phase: N/A
Study type: Interventional

In this study, the investigators sought to determine whether an acoustic cardiographic assessment of heart function is equivalent to Doppler-echocardiography in patients who are treated with cardio-toxic cytostatic agents.