All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Reported results | 2004-000327-15 | A Phase 3 Multicenter, Open-label, Randomized Study of XL119 Versus 5-Fluorouracil (5-FU) plus Leucovorin (LV) in Subjects with Advanced Biliary Tumors Not Amenable to Conventional Surgery | 2006-12-06 | due-trials |
Reported results | 2005-000137-37 | Single Dose, Randomized, Double-Blind, Parallel Group, Multicenter Study of Palonosetron 0.25 mg, 0.50 mg and 0.75 mg Administered by the Oral Route versus Palonosetron 0.25 mg IV for the Prevention o... | 2006-08-31 | due-trials |
Reported results | 2005-000298-23 | A Randomized, Double-blind, Multicenter, Parallel Group, Balanced, Stratified Phase 3 Study to Evaluate the Efficacy and the Safety of Single IV Doses of Palonosetron 0.025 mg, 0.050 mg, and 0.075 mg ... | 2006-05-03 | due-trials |
Reported results | 2005-000583-28 | EFFICACY AND TOLERABILITY OF NIMESULIDE FOR THE TREATMENT OF MIGRAINE TTACKS: A RANDOMISED, MULTICOUNTRY, DOUBLE BLIND, PLACEBO CONTROLLED, CROSS-OVER TRIAL | 2007-01-07 | due-trials |
Reported results | 2005-001944-21 | Multicenter, Phase III, Open-Label, Uncontrolled Study to Assess the Safety and Efficacy of a Single Oral Dose of Palonosetron 0.75 mg in the Prevention of Chemotherapy Induced Nausea and Vomiting in ... | 2006-04-27 | due-trials |
Reported results | 2005-002641-39 | Open-Label Pilot Study to Evaluate the Efficacy of Palonosetron Associated with Aprepitant (Emend) and Dexamethasone in Preventing Nausea and Vomiting Induced by Highly Emetogenic Chemotherapy (HEC) | 2007-02-19 | due-trials |
Reported results | 2005-002643-89 | Double-blind Study to Compare the Efficacy of Palonosetron with or without the use of Dexamethasone on Days 2 and 3, in the Prevention of Nausea and Vomiting Induced by Moderately Emetogenic Chemother... | 2008-04-01 | due-trials |
Reported results | 2008-003190-41 | A Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Prospective Study to Assess the Efficacy, Safety and Tolerability of Three Oral Doses of Netupitant Given Once a Day (50, ... | 2011-08-31 | due-trials |
Reported results | 2008-007827-14 | Multicenter, Phase IV, Open-Label, Uncontrolled Study to Assess the Efficacy and Safety of a Single Intravenous Dose of Palonosetron 0.25 mg (Aloxi, Onicit, Paloxi) in the Prevention of Chemotherapy-I... | 2011-04-30 | due-trials |
Reported results | 2009-016775-30 | A phase III multicenter, randomized, double-blind, double-dummy, active-controlled, parallel group study of the efficacy and safety of oral netupitant administered in combination with palonosetron and... | 2012-11-06 | due-trials |
Reported results | 2010-022223-29 | Single-dose, multicenter, randomized, double-blind, double-dummy, parallel group study to assess the efficacy and safety of oral palonosetron 0.50 mg compared to I.V. palonosetron 0.25 mg administere... | 2012-11-14 | due-trials |
Listed as ongoing, but also has a completion date and reported results | 2010-022872-30 | A multicenter, randomized, double-blind, parallel group study to evaluate the efficacy and safety of two different doses of palonosetron compared to ondansetron in the prevention of CINV in pediatric ... | 2012-10-25 | bad-data |
Reported results | 2010-022971-79 | A Multicenter, Double-blind, Double-dummy, Randomized, Parallel Group, Stratified Study to Evaluate the Efficacy and Safety of a Single IV Dose of Palonosetron Compared to a Single IV Dose of Ondanset... | 2012-03-27 | due-trials |
Reported results | 2010-023297-39 | A phase III, multicenter, randomized, double-blind, unbalanced (3:1) active control study to assess the safety and describe the efficacy of netupitant and palonosetron for the prevention of chemothera... | 2012-09-13 | due-trials |
Reported results | 2010-023648-34 | Anamorelin HCl in the Treatment of Non-Small Cell Lung Cancer – Cachexia (NSCLC-C): A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase III Study to Evaluate the Safety and Effic... | 2014-10-22 | due-trials |
Reported results | 2010-023649-31 | Anamorelin HCl in the Treatment of Non-Small Cell Lung Cancer – Cachexia (NSCLC-C): A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase III Study to Evaluate the Safety and Efficacy of ... | 2014-10-10 | due-trials |
Reported results | 2010-023650-36 | Anamorelin HCl in the Treatment of Non-Small Cell Lung Cancer ? Cachexia (NSCLC-C): An Extension Study (ROMANA-3). HCl de Anamorelina en el tratamiento de caquexia asociada al carcinoma broncopulmo... | 2014-06-12 | due-trials |
Reported results | 2011-004981-13 | Phase II, Double-blind, Randomized, Two-stage, Placebo-controlled Proof of Concept Study in Colorectal Cancer Patients Receiving 5-FU-based Chemotherapy to Assess the Efficacy of Elsiglutide (ZP1846) ... | 2013-01-11 | due-trials |
Reported results | 2014-000998-39 | Randomized, double-blind, parallel group, placebo-controlled, dose finding study in colorectal cancer patients receiving 5-FU-based chemotherapy to assess the efficacy of different doses of s.c. elsig... | 2016-02-09 | due-trials |
Reported results | 2015-001747-37 | A phase 3, single-dose, multicenter, randomized, double-blind, parallel group study to assess the efficacy and safety of palonosetron 0.25 mg administered as a 30-minute IV infusion compared to palono... | 2016-03-09 | due-trials |
Reported results | 2015-001800-74 | A phase 3, multicenter, randomized, double-blind, active control study to evaluate the safety and efficacy of IV pro-netupitant/palonosetron (260 mg/0.25 mg) combination for the prevention of chemothe... | 2016-08-02 | due-trials |
Reported results | 2016-004724-34 | A Phase III, Double-Blind, Placebo-Controlled, Multicenter, Randomized Study Of Pracinostat In Combination With Azacitidine In Patients > o uguale a18 Years With Newly Diagnosed Acute Myeloid Leukemi... | 2020-07-02 | due-trials |
Listed as ongoing, but also has a completion date and reported results | 2018-002926-22 | A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Anamorelin HCL for the Treatment of Malignancy Associated Weight Loss and Anorexia in A... | 2023-02-11 | bad-data |
Listed as ongoing, but also has a completion date and reported results | 2018-002927-40 | A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Anamorelin HCl for the Treatment of Malignancy Associated Weight Loss and Anorexia in a... | 2022-12-27 | bad-data |
Listed as ongoing, but also has a completion date | 2019-004686-41 | MyRisk: Efficacy and safety evaluation of oral Akynzeo® in patients receiving MEC at high risk of developing CINV based on a prediction tool. A multinational and multicenter study. | 2024-07-02 | bad-data |
Trial is outside EEC, and reported results | 2020-003730-20 | A multicenter, multinational, randomized, double-blind, pharmacokinetic and pharmacodynamic (PK/PD) dose-finding study of oral netupitant administered concomitantly with oral palonosetron in pediatric... | bad-data | |
Exempt | 2021-005614-34 | A Phase 1b/2, Multicenter, Open-Label Study of Oral Infigratinib in Pediatric Subjects with Advanced Solid and Central Nervous System (CNS) Tumors (Phase 1b) and in Subjects with Recurrent or progress... | not-yet-due |