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NCT ID: NCT02399917 Terminated - Clinical trials for Refractory Acute Myeloid Leukemia

Lirilumab and Azacitidine in Treating Patients With Refractory or Relapsed Acute Myeloid Leukemia

Start date: April 20, 2015
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects lirilumab and azacitidine and to see how well they work in treating patients with acute myeloid leukemia that has not responded to treatment or has returned after a period of improvement. Monoclonal antibodies, such as lirilumab, may interfere with the ability of cancer cells to grow and spread. Drugs used in chemotherapy, such as azacitidine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving lirilumab with azacitidine may be an effective treatment for relapsed or refractory acute myeloid leukemia.

NCT ID: NCT02399319 Terminated - Clinical trials for Anterior Pelvic Ring Injury With Symphysis Disruption

Comparison of INFIX and Plating for Pelvic Ring Injuries With Symphysis Disruptions

Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare subcutaneous internal fixation and open plating of the symphysis in patients with a disruption of the symphysis requiring stabilization.

NCT ID: NCT02398500 Terminated - Clinical trials for Age-related Macular Degeneration (AMD)

Safety Tolerability and Efficacy of Intravitreal LMG324 in the Treatment of Neovascular Age-Related Macular Degeneration

Start date: July 22, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this first-in-human study is to evaluate the safety and tolerability of single ascending doses of LMG324 to determine the maximum tolerated dose (MTD) in neovascular age-related macular degeneration (nvAMD) subjects. Enrollment will be expanded at a safe and tolerated dose in treatment naïve nvAMD subjects to compare a single intravitreal (IVT) dose of LMG324 to ranibizumab 0.5 mg administered every 4 weeks for change from baseline in best-corrected visual acuity (BCVA) at Week 12 (Day 85).

NCT ID: NCT02397941 Terminated - Diastasis Recti Clinical Trials

Diastasis Recti Abdominis and Abdominal Muscles

Start date: December 2015
Phase:
Study type: Observational

Purpose of the study is the assessment of interrectal distance and dimensions of the muscles of the lateral abdominal wall in pregnant and non-pregnant women

NCT ID: NCT02394782 Terminated - Clinical trials for Multiple Sclerosis, Relapsing-remitting

Observational Study of Rebismart®2.0 + MSdialog™ in Subjects With Remitting Multiple Sclerosis (ADHERQOL)

ADHERQOL
Start date: February 2015
Phase: N/A
Study type: Observational

This is a 24-month, observational, prospective, multinational, multicenter study to determine the relationship between the relapse (percentage of relapse free subjects) and adherence in subjects diagnosed with RRMS treated with Rebif (interferon beta-1a) using the RebiSmart®2.0 and MSdialog™.

NCT ID: NCT02392377 Terminated - Clinical trials for Stage IIIB Esophageal Adenocarcinoma

Molecular Phenotyping in Predicting Response in Patients With Stage IB-III Esophageal Cancer Receiving Combination Chemotherapy

Start date: February 2015
Phase: Phase 2
Study type: Interventional

This randomized pilot phase II trial studies how well molecular phenotyping works in predicting response in patients with stage IB-III esophageal cancer who are receiving carboplatin and paclitaxel or oxaliplatin, leucovorin calcium, and fluorouracil. Studying the genes in a patients tumor cells before and after chemotherapy may help in understanding if there are specific features of the tumor cells that make a person more or less likely to respond to treatment and how these features may be affected by treatment.

NCT ID: NCT02390362 Terminated - Clinical trials for Steroid Dependent Nephrotic Syndrome

Randomized Trial Comparing Rituximab Against Mycophenolate Mofetil in Children Wtih Refractory Nephrotic Syndrome

RAMP
Start date: January 2015
Phase: Phase 3
Study type: Interventional

We hypothesize that the anti-CD20 monoclonal antibody Rituximab will be more effective than MMF in maintaining remission in children with frequent relapsing or steroid dependent nephrotic syndrome who have had one relapse while receiving MMF. We will conduct a randomized study comparing two Rituximab infusions and continued MMF treatment. We plan to enroll 64 to have a comparater group of 58 (29 in each arm).

NCT ID: NCT02388932 Terminated - Clinical trials for Recurrent Laryngeal Squamous Cell Carcinoma

Stereotactic Body Radiation Therapy in Treating Patients With High Risk Locally Advanced Head and Neck Cancer

Start date: March 3, 2015
Phase: N/A
Study type: Interventional

This phase I trial studies the side effects and best dose of stereotactic body radiation therapy (SBRT) in treating participants with head and neck cancer that has spread from where it started to nearby tissue or lymph nodes and is at high risk for continuing to spread because the participant cannot undergo standard chemotherapy. Stereotactic body radiation therapy is a specialized radiation therapy that delivers radiation directly to the tumor in smaller doses over several days, which may kill more tumor cells and cause less damage to normal tissue.

NCT ID: NCT02386111 Terminated - Neoplasms Clinical Trials

A Study of Varlilumab (Anti-CD27) and Sunitinib in Patients With Metastatic Clear Cell Renal Cell Carcinoma

Start date: May 2015
Phase: Phase 1
Study type: Interventional

This is a study to determine the clinical benefit (how well the drug works), safety, and tolerability of combining varlilumab and sunitinib. The study will enroll patients with metastatic clear cell renal cell carcinoma.

NCT ID: NCT02385266 Terminated - Clinical trials for Chronic Prostatitis With Chronic Pelvic Pain Syndrome

Treating Urological Chronic Pelvic Pain Syndrome (UCPPS) Pain

UCPPS
Start date: September 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of D-Cycloserine versus placebo treatment in reducing pain from urological chronic pelvic pain syndrome (UCPPS).