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Search clinical trials for: Vasomera
Total 2 results
PhaseBio Pharmaceuticals Inc.
Completed
Phase 1, Randomized, Double-Blind, Placebo-Controlled Exploratory Study That Will Assess the Safety, Tolerability, Pharmacokinetics and Hemodynamic Response to a Single 30 Minute Intravenous Infusion of Vasomera™ (PB1046) in Adult Subjects With Stage 1 or 2 Essential Hypertension
Essential Hypertension
United States
PhaseBio Pharmaceuticals Inc.
Completed
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Response of Vasomera (PB1046) Injection Following a Single Subcutaneous Dose in Subjects With Stage 1 or 2 Essential Hypertension
Essential Hypertension
United States
Sponsors and Collaborators
Secretariat of Public Education (SEP)
Innovative Therapies, Inc.
Ozden Gokcek
Facultad de Estudios Superiores Aragón UNAM
Camille Levy
Tarek Alsaied
Giovanni Mirabella
CellMaxLife
Jorge Orduña-Valls
Healthy Life
Monroe Carell Jr. Children's Hospital at Vanderbilt
Colorado Childrens Hospital
Ringerike sykehus, Vestre Viken HF
Clinical Oncology department. Elmansoura University.
Amira Hussin Hussin Mohammed
Craving Change
Institute of Cancer Research (ICR), United Kingdom
First People's Hospital of Shenyang
Azienda Unità Sanitaria Locale Reggio Emilia
Holger Dressel
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Medical Conditions
Asthma, Allergic
Angiotensin-Converting Enzyme Inhibitors
Post-operative Intercostal Neuralgia
Human Herpes Virus-6 Infection
Triple Negative Breast Cancer, TNBC
Postoperative Analgesic Demand
Established Atherosclerotic Cardiovascular Disease (ASCVD) or ASCVD Risk
Impulse-Control Disorders
Homologous Recombination Deficient Solid Tumors
Acute Myelogenous Leukemia (AML or ANLL)
Emergency Geriatric Care
CYP2C19 Poor
Body Height
Drainage Procedure
Skin and Subcutaneous Tissue Infection
MINI MENTAL STATE EXAMINATION TEST
Rectal Adenocarcinoma
Peripheral Neuropathy Associated With Anti-myelin Associated Glycoprotein Antibodies (Anti-MAG Neuropathy)
Ascorbic Acid
Ventilator Induced Diaphragm Dysfunction
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Drug Interventions
Topical Solution
Enfuvirtide-intensified HAART
Prolonged release (PR) OROS methylphenidate 72 mg
RBS2418
AZD7325
Fluvastatin
Bevacizumab standard of care
Background regimen (BR) for MDR-TB (multi-drug resistant tuberculosis)
Standard of care
Xenon
Octreotide
GW-1000-02
Trastuzumab
Antithymocyte globulin (Rabbit)
Tenecteplase
AMT-101 (oral)
Ascorbic Acid
Leucovorin
Luliconazole Cream 1% - 2 wks
BMS-770767
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Worldwide Clinical Trials
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PSI
Syneos Health
Caidya
All CROs in France
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