MedPath

Commons, Marty

🇺🇸United States
Ownership
-
Employees
-
Market Cap
-
Website

4EVER - Efficacy, Safety, Health Economics, Translational Research of Postmenopausal Women With Estrogen Receptor Positive Locally Advanced or Metastatic Breast Cancer

Phase 3
Completed
Conditions
Metastatic Breast Cancer
Interventions
First Posted Date
2012-06-22
Last Posted Date
2017-02-23
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
301
Registration Number
NCT01626222
Locations
🇩🇪

Novartis Investigative Site, Wuppertal, Germany

Evaluate Efficacy and Safety of Fingolimod 0.5 mg Orally Once Daily Versus Placebo in Chronic Inflammatory Demyelinating Polyradiculoneuropathy Patients.

Phase 3
Completed
Conditions
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Interventions
Drug: Placebo Comparator
First Posted Date
2012-06-21
Last Posted Date
2017-10-30
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
106
Registration Number
NCT01625182
Locations
🇬🇧

Novartis Investigative Site, Newcastle Upon Tyne, United Kingdom

A National Multi-center Randomized, Open Label Study to Evaluate Efficacy and Safety of Everolimus With EC-MPS Compared to Standard Treatment Combination Tacrolimus and EC-MPS in de Novo Liver Transplant Recipients

Phase 3
Completed
Conditions
Liver Transplantation
Interventions
First Posted Date
2012-06-21
Last Posted Date
2016-04-27
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
188
Registration Number
NCT01625377
Locations
🇫🇷

Novartis Investigative Site, Villejuif, France

Safety and Tolerability of Intravenous LFG316 in Wet Age-related Macular Degeneration (AMD).

Phase 2
Terminated
Conditions
Neovascular Age-related Macular Degeneration
Interventions
Drug: Placebo
First Posted Date
2012-06-21
Last Posted Date
2020-12-19
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
1
Registration Number
NCT01624636
Locations
🇺🇸

Novartis Investigative Site, Cleveland, Ohio, United States

Evaluation of Patient Retention of Fingolimod vs. Currently Approved Disease Modifying Therapy in Patients With Relapsing Remitting Multiple Sclerosis.

Phase 4
Completed
Conditions
Relapsing Remitting Multiple Sclerosis
Interventions
Drug: Disease Modifying therapy
First Posted Date
2012-06-20
Last Posted Date
2021-01-05
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
881
Registration Number
NCT01623596
Locations
🇵🇷

Novartis Investigative Site, Guaynabo, Puerto Rico

ENGYNE Exploring Gilenya in Patients With Neutralizing Antibodies Against Interferon

Phase 4
Withdrawn
Conditions
Multiple Sclerosis
Interventions
First Posted Date
2012-06-18
Last Posted Date
2017-04-20
Lead Sponsor
Novartis Pharmaceuticals
Registration Number
NCT01621269

A Study of LCZ696 in Subjects With Mild and Moderate Hepatic Impairment Compared With Normal Healthy Volunteers

Phase 2
Completed
Conditions
Hepatic Impairment
Interventions
First Posted Date
2012-06-18
Last Posted Date
2015-08-10
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
32
Registration Number
NCT01621633
Locations
🇩🇪

Novartis Investigative Site, Grunstadt, Germany

Clinical Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LEZ763

Phase 1
Completed
Conditions
Type II Diabetes
Interventions
First Posted Date
2012-06-14
Last Posted Date
2020-12-17
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
220
Registration Number
NCT01619332
Locations
🇺🇸

Novartis Investigative Site, San Antonio, Texas, United States

Efficacy, Safety and Pharmacokinetics of Artemether-lumefantrine Dispersible Tablet in the Treatment of Malaria in Infants < 5 kg

Phase 2
Completed
Conditions
Acute Uncomplicated Falciparum Malaria
Interventions
Drug: Artemether-lumefantrine (COA566)
First Posted Date
2012-06-14
Last Posted Date
2015-06-17
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
20
Registration Number
NCT01619878
Locations
🇧🇫

Novartis Investigative Site, Burkina Faso, Burkina Faso

🇹🇬

Novartis investigative site, Lome, Togo

A Randomized,Double Blind, Placebo Controlled Study to Assess Efficacy,Safety and Tolerability of BGG492 in Migraine Prevention

Phase 2
Withdrawn
Conditions
Patients With Migraine Equal of /More Than 3 and Equal of/ Less Than 12 Migraine Attacks/4 Weeks for Each of the Last 6 Months Preceding the Screening
Interventions
Drug: Placebo
First Posted Date
2012-06-13
Last Posted Date
2017-04-20
Lead Sponsor
Novartis Pharmaceuticals
Registration Number
NCT01617941
© Copyright 2025. All Rights Reserved by MedPath