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Generated: December 14, 2018

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CLINICAL TRIALS PROFILE FOR KYTRIL

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Clinical Trials for Kytril

Trial ID Title Status Sponsor Phase Summary
NCT00005024 Granisetron to Prevent Nausea and Vomiting After Chemotherapy in Patients With Malignant Disease Unknown status National Cancer Institute (NCI) Phase 3 RATIONALE: Antiemetic drugs such as granisetron may help to prevent nausea and vomiting in patients treated with chemotherapy. PURPOSE: Randomized phase III trial to compare the effectiveness of granisetron with that of a placebo in preventing nausea and vomiting after chemotherapy in patients who have malignant disease.
NCT00005024 Granisetron to Prevent Nausea and Vomiting After Chemotherapy in Patients With Malignant Disease Unknown status Jonsson Comprehensive Cancer Center Phase 3 RATIONALE: Antiemetic drugs such as granisetron may help to prevent nausea and vomiting in patients treated with chemotherapy. PURPOSE: Randomized phase III trial to compare the effectiveness of granisetron with that of a placebo in preventing nausea and vomiting after chemotherapy in patients who have malignant disease.
NCT00231478 A Study of Kytril (Granisetron) in the Prevention of Post-Operative Nausea and Vomiting (PONV) in Pediatric Subjects Undergoing Tonsillectomy or Adenotonsillectomy Completed Hoffmann-La Roche Phase 4 This 2 arm study will evaluate the efficacy and safety of a single intravenous injection of Kytril in preventing postoperative nausea and vomiting (PONV) in children. Patients will be randomized to receive a single dose of either 20 micrograms or 40 micrograms Kytril intravenously (iv) 15 minutes prior to the end of surgery with general anesthesia for tonsillectomy or adenotonsillectomy. The anticipated time on study treatment is <3 months, and the planned sample size was 170 patients.
NCT00256841 Hypo-Hyperfractionated Chest Radiation for Non Small Cell Lung Cancer With Taxotere/Xeloda Combination Chemotherapy Withdrawn Clinical Oncology Research Associates Phase 1/Phase 2 The study is designed for patients with non small cell lung cancer whose cancer is too advanced and therefore cannot be operated with the goal of completely removing the cancer. At this stage of the disease, most patients cannot be cured from the disease, however, treatment can help to live longer and better by keeping the cancer under control. For that purpose, patients traditionally receive radiation therapy or chemotherapy or both treatments in succession. Recently, the administration of both treatment methods given concurrently showed somewhat better results when compared to successive administration. In some studies the drug Taxotere together with radiation performed well in keeping the cancer better under control. Combination of the drug Taxotere together with a compound called 5-FU either as continuous infusion or in its oral form of a pill called "Xeloda" enhanced its anti cancer activity substantially. One goal of this study is to investigate how much of the combination can be given in conjunction with chest radiation. Using X-rays, the study will also evaluate how much shrinkage of the cancer is caused by this treatment directly at the tumor site and other areas where the cancer may have also spread. In this study the radiation will be given on only one day per week in two sessions, rather than divided over five days per week (Monday through Friday) as it is more commonly used. However, both schedules have been found to be equally effective. The treatment program will use increasing doses of the 5-FU medication, either as infusion or as pill to find the highest dose that is tolerated. Once the highest tolerated dose is determined, subsequent patients who will be enrolled will continue to be treated at that dose level. The dose of the drug Taxotere will remain the same throughout. Hypothesis: Our previous research suggests that the combination of Taxotere and 5-FU given together with weekly chest radiation will provide a more convenient form of treatment than the conventional approach and also be at least similar in its efficacy.
NCT00360828 Phase II Study of Irinotecan HCI for Recurrent Anaplastic Astrocytomas, Mixed Malignant Gliomas, and Oligodendrogliomas Terminated H. Lee Moffitt Cancer Center and Research Institute Phase 2 Phase 2 trial to explore the efficacy and safety of irinotecan (CPT-11). Also administered at each cycle was zofran/Kytril/Anzemet, decadron, and IV atropine. At each cycle, patient exams and interviews as well as lab results were to help the research team to determine the symptomatic side effects of the treatment. Recorded past toxicities were to be compared with current side effects.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Kytril

Condition Name

Condition Name for Kytril
Intervention Trials
Vomiting 3
Chemotherapy-induced Nausea and Vomiting 3
Healthy 2
Nausea 2
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Condition MeSH

Condition MeSH for Kytril
Intervention Trials
Vomiting 10
Nausea 8
Glioma 2
Postoperative Nausea and Vomiting 2
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Clinical Trial Locations for Kytril

Trials by Country

Trials by Country for Kytril
Location Trials
United States 20
Canada 2
Israel 1
France 1
Korea, Republic of 1
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Trials by US State

Trials by US State for Kytril
Location Trials
Massachusetts 4
Nebraska 2
Pennsylvania 2
Florida 2
Minnesota 1
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Clinical Trial Progress for Kytril

Clinical Trial Phase

Clinical Trial Phase for Kytril
Clinical Trial Phase Trials
Phase 4 3
Phase 3 5
Phase 2 3
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Clinical Trial Status

Clinical Trial Status for Kytril
Clinical Trial Phase Trials
Completed 8
Unknown status 3
Terminated 2
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Clinical Trial Sponsors for Kytril

Sponsor Name

Sponsor Name for Kytril
Sponsor Trials
Tesaro, Inc. 3
Teva Pharmaceuticals USA 2
Roxane Laboratories 2
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Sponsor Type

Sponsor Type for Kytril
Sponsor Trials
Industry 10
Other 8
NIH 1
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Serving hundreds of leading biopharmaceutical companies globally:

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