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NCT ID: NCT01788982 Completed - Clinical trials for Differentiated Thyroid Cancer (DTC)

Nintedanib(BIBF1120) in Thyroid Cancer

Start date: May 2014
Phase: Phase 2
Study type: Interventional

For the treatment of thyroid cancer with the so called targeted therapy the angiogenesis pathway has several potential targets. The Receptors for Vascular endothelial growth factor (VEGF) and especially VEGFR-2 is considered to be crucial for the initiation of the formation as well as the maintenance of tumor vasculature. In thyroid cancer these VEGF receptors (VEGFR-1, VEGFR-2), VEGF itself and receptors of the fibroblast growth factor (FGF) and for the platelet-derived growth factor (PDGF) are often overexpressed. Other cells as pericytes and smooth muscle cells that are also involved in tumor angiogenesis express these receptors as well. Inhibitors of the VEGFR or PDGFR pathway have been tested in thyroid cancer with positive results. However there is no treatment that is generally considered as standard of care for patients with differentiated thyroid cancer (DTC) or medullar thyroid cancer (MTC) who have progressed on one line of therapy. The classical cytotoxic chemotherapy has not shown a clinically meaningful benefit yet. Nintedanib is a triple angiogenesis inhibitor which inhibits receptors of VEGF, FGF and PDGF. Therefore it might act not only on endothelial cells but also on pericytes and smooth muscle cells. Nintedanib also interacts with other kinases such as RET. Because of this multi-kinase activity rationale exists to investigate the effect in MTC and DTC. Because it targets these three major angiogenesis signaling pathways it might prevent further tumor growth and related tumor escape mechanisms. Therefore nintedanib may be active in patients who have progressed on agents that target only one pathway.

NCT ID: NCT01788774 Completed - Schizophrenia Clinical Trials

Pharmacokinetic, Safety, and Tolerability Study of Risperidone ISM® at Different Dose Strengths

PRISMA-1
Start date: April 2013
Phase: Phase 1
Study type: Interventional

This clinical trial is designed to evaluate different dosages of risperidone ISM, a new long-acting injectable form.

NCT ID: NCT01788670 Completed - Clinical trials for Contribution of Ethanol on Hydroxytyrosol Formation

Relevance of the Ethanol Dose in the Generation of Endogenous Hydroxytyrosol

Start date: May 2009
Phase: Phase 1
Study type: Interventional

Health benefits for humans derived from low dose intake of ethanol could partially be explained by its interaction with dopamine (DA) oxidative metabolism. Ethanol is expected to induce an increase in the formation of a DA minor metabolite: DOPET (hydroxytyrosol). Hydroxytyrosol is one of the most potent antioxidants present in Mediterranean Diet. The study is aimed at establishing the contribution of ethanol on hydroxytyrosol formation.

NCT ID: NCT01788527 Completed - Clinical trials for Type 1 Diabetics Who Are Pregnant or Planning Pregnancy

Continuous Glucose Monitoring in Women With Type 1 Diabetes in Pregnancy Trial

CONCEPTT
Start date: March 2013
Phase: N/A
Study type: Interventional

The primary objective of the study is to determine if RT CGM (Real Time-Continuous Glucose Monitoring) can improve glycemic control in women with T1D who are pregnant or planning pregnancy.

NCT ID: NCT01788046 Completed - Clinical trials for Hyperparathyroidism, Secondary

Efficacy and Safety of Etelcalcetide (AMG 416) in the Treatment of Secondary Hyperparathyroidism (SHPT) in Patients With Chronic Kidney Disease (CKD) on Hemodialysis

Start date: March 12, 2013
Phase: Phase 3
Study type: Interventional

This study is designed to assess the efficacy and safety of etelcalcetide (AMG 416) compared with placebo in the treatment of SHPT in CKD patients receiving hemodialysis.

NCT ID: NCT01787552 Completed - Clinical trials for Hematologic Diseases

A Phase Ib/II Dose-finding Study to Assess the Safety and Efficacy of LDE225 + INC424 in Patients With MF

Start date: May 8, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this phase Ib/II clinical trial was to: a) evaluate the safety of the co-administration of LDE225 and INC424 in myelofibrosis patients and establish a maximum tolerated dose and/or Recommended Phase II dose of the combination and b) to assess the efficacy of the co-administration of LDE225 and INC424 on spleen volume reduction.

NCT ID: NCT01787435 Completed - Asthma in Offspring Clinical Trials

Acid-suppressing Drugs Pregnancy Asthma Offspring Study

Start date: June 2012
Phase: N/A
Study type: Observational

The purpose of this study is 1. To estimate the association between prenatal exposure to proton pump inhibitors (PPIs) and the risk of asthma during childhood. 2. To estimate the association between prenatal exposure to H2-receptor antagonists (H2RAs) and the risk of asthma during childhood.

NCT ID: NCT01786668 Completed - Clinical trials for Ankylosing Spondylitis

Dose-Ranging Study Of Tofacitinib In Adults With Active Ankylosing Spondylitis

Start date: April 2013
Phase: Phase 2
Study type: Interventional

This is the first study of oral tofacitinib in adults with active ankylosing spondylitis. It is designed to obtain information on the efficacy and safety of 3 different doses of tofacitinib.

NCT ID: NCT01786486 Completed - Stroke Clinical Trials

AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol

ACPR
Start date: August 2009
Phase:
Study type: Observational [Patient Registry]

The objective of the AMPLATZER Cardiac Plug (ACP) Registry Long Term Follow-up study is to evaluate long term performance of the ACP in closure of the Left Atrial Appendage (LAA) in subjects with nonvalvular atrial fibrillation and assess adverse events up to two (2) or more years post implant.

NCT ID: NCT01786083 Completed - Anxiety Clinical Trials

Caring for Family Caregivers:a Research-action Study

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

The purpose of this study is to evaluate the effectiveness of the Problem Solving Technique (PST) in reducing symptoms of anxiety and depression among primary caregivers of chronically ill patients. And also to describe and evaluate the process carried out by nurses when implementing the PST as a useful tool for care for family caregivers.