Clinical Trials Sponsored by Omnispec clinical research Inc

Total 498 results

Clinical Research Management, Inc.

Unknown

Clinical Trial to Evaluate the Efficacy and Safety of Convalescent Plasma for Ebola Treatment (EVD001)

Ebola Virus Disease

Liberia
Clinical Research Consultants, Inc.

Completed

Influence of DisCoVisc Ophthalmic Viscosurgical Device (OVD) on Intraoperative Aberrometry Readings

Cataract

United States
Evolus, Inc.
ethica Clinical Research Inc.

Completed

Study to Demonstrate Safety and Duration of Effect of 40 Units of PrabotulinumtoxinA-xvfs to Treat Glabellar Lines

Glabellar Frown Lines

United States
Scynexis, Inc.
ethica Clinical Research Inc.

Completed

Safety and Efficacy of Oral Ibrexafungerp (SCY-078) vs. Oral Fluconazole in Subjects With Vulvovaginal Candidiasis

Vulvovaginal Candidiasis

Dominican Republic
Cutera Inc.
ethica Clinical Research Inc.

Recruiting

A Study of a Laser for the Treatment of Acne Vulgaris

Acne Vulgaris

Canada
Davita Clinical Research
Nuvo Research Inc.

Terminated

Effect of Including Synera® in Discussions on Dialysis Access Conversion in Patients With Needle Phobias

Phobic Disorders | Needle Phobia

United States
Freshly, Inc.
Biofortis Clinical Research, Inc.

Not yet recruiting

A Study to Assess the Effects of Freshly Fit Meals on Body Weight and Wellness in Overweight and Obese Adults

Weight Loss

United States
Evofem Inc.
Clinical Research Management, Inc.

Completed

Phase 2B/3 Double-blinded Placebo-controlled

Chlamydia Trachomatis Infection

United States
Xoft, Inc.
Eminence Clinical Research, Inc.

Unknown

Electronic Brachytherapy (eBx)-Mohs Matched Pair - Cohort Study A Multi-Center Retrospective-Prospective Matched Pairs Cohort Study to Assess Long-term Clinical Outcomes of Non-melanoma Skin Cancer Patients Treated With eBx Compared to Non-melanoma Skin Cancer Patients Treated With Mohs Surgery

Nonmelanoma Skin Cancer

United States
Nutrisystem, Inc.
Biofortis Clinical Research, Inc.

Completed

Study to Evaluate Effects of a Weight Loss Program in Different Formats on Healthy Adults

Weight Loss | Overweight and Obesity
Cognivue, Inc.
Velocity Clinical Research

Completed

Cognitive Testing in Diverse Populations to Further the Objective and Clinical Understanding of Cognivue Study (FOCUS)

Cognitive Change

United States
CytoDyn, Inc.
Amarex Clinical Research

Active, not recruiting

Basket Study of Leronlimab (PRO 140) in Patients With CCR5+ Locally Advanced or Metastatic Solid Tumors

Solid Tumor, Adult

United States
Xencor, Inc.
ICON Clinical Research

Completed

PH 1 Study to Evaluate Safety and Tolerability of XmAb14045 in Patients With CD123-expressing Hematologic Malignancies

Acute Myelogenous Leukemia | Blastic Plasmacytoid Dendritic Cell Neoplasm | B-cell Acute Lymphoblastic Leukemia | Chronic Myeloid Leukemia, Blast Crisis

United States
DiaSorin Inc.
ICON Clinical Research

Completed

Helicobacter Pylori Sample Collection Protocol Pre Therapy Subjects

Nausea | Abdominal Pain | Weight Loss | Helicobacter Pylori Infection | Gastric Ulcer | Stomach Ulcer | Loss of Appetite | Bloating

United States, Italy
CytoDyn, Inc.
Amarex Clinical Research

No longer available

An Expanded Access Protocol for a Single Subject Who Has Completed 24-Weeks of Treatment in PR0140_CD02 Study (CD02_EA)

HIV

United States
Cargill
Biofortis Clinical Research, Inc.

Completed

A Randomized, Controlled, Crossover Study to Assess the Glucose and Insulin Excursions of a Test Fiber

Healthy

United States
BioChemics, Inc.
Harrison Clinical Research

Withdrawn

Safety and Efficacy Study of BC-DN-01 in Painful Diabetic Peripheral Neuropathy

Diabetic Neuropathy, Painful

United Kingdom
Zarbee's Inc.
Advanced Clinical Research

Terminated

A Novel Formulation of Pasteurized Maple Cough Syrup Compared With Placebo on Nocturnal Cough and Sleep Quality in Infants With Upper Respiratory Infection

Cough | Upper Respiratory Infection | Nocturnal Cough

United States
CytoDyn, Inc.
Amarex Clinical Research

Completed

Double Blind, Placebo Controlled Study of Safety and Efficacy of Leronlimab in Patients With "Long" COVID-19

Coronavirus Disease 2019

United States
Xencor, Inc.
ICON Clinical Research

Active, not recruiting

Study to Evaluate Safety and Tolerability of XmAb13676 (Plamotamab) in Patients With CD20-expressing Hematologic Malignancies

Chronic Lymphocytic Leukemia | B-cell Non-Hodgkins Lymphoma

United States, France, Korea, Republic of, United Kingdom
CytoDyn, Inc.
Amarex Clinical Research

Terminated

A Study of Acute Graft-Versus-Host Disease (GVHD) in Patients Undergoing Allogeneic Stem-Cell Transplantation (GVHD)

Graft Vs Host Disease

United States
Xencor, Inc.
ICON Clinical Research

Completed

A Study of XmAb®22841 Monotherapy & in Combination w/ Pembrolizumab in Subjects w/ Selected Advanced Solid Tumors (DUET-4)

Melanoma | Renal Cell Carcinoma | Nasopharyngeal Carcinoma | Small Cell Lung Carcinoma | Hepatocellular Carcinoma | Fallopian Tube Cancer | Non-small Cell Lung Carcinoma | Squamous Cell Carcinoma of the Head and Neck | Triple Negative Breast Cancer | Epithelial Ovarian Cancer | Intrahepatic Cholangiocarcinoma and other conditions

United States
CytoDyn, Inc.
Amarex Clinical Research

Withdrawn

Leronlimab in Combination With Regorafenib in Patients With CCR5+, Metastatic Colorectal Cancer

Colorectal Cancer | Microsatellite Stable | Metastatic | CCR5
CytoDyn, Inc.
Amarex Clinical Research

Active, not recruiting

Leronlimab (PRO 140) Combined With Carboplatin in Patients With CCR5+ mTNBC

Triple Negative Breast Neoplasms

United States
Cleerly, Inc.
CPC Clinical Research

Recruiting

A Randomized Comparison of Stage-Based Care Versus Risk Factor-Based Care for Prevention of Cardiovascular Events (TRANSFORM)

Diabetes Mellitus, Type 2 | Metabolic Syndrome | PreDiabetes

United States
CytoDyn, Inc.
Amarex Clinical Research

Completed

Treatment Substitution With PRO 140 Monotherapy in Adult Subjects With HIV-1 Infection

HIV | Human Immunodeficiency Virus

United States
Xencor, Inc.
ICON Clinical Research

Completed

Safety, Tolerability and PK of a Single Subcutaneous Injection of XmAb27564 in Healthy Volunteers

Safety in Healthy Volunteers

United States
CytoDyn, Inc.
Amarex Clinical Research

Completed

Leronlimab (PRO 140) in Patients With Nonalcoholic Steatohepatitis (NASH)

Nonalcoholic Steatohepatitis (NASH)

United States
Safeheal
Clinical Research Consultants, Inc.

Completed

Retrospective Study of Surgical Complications in Patients With Defunctioning Stoma After Low Anterior Resection (LAR)

Rectal Cancer

United States, Canada
DiaSorin Inc.
ICON Clinical Research

Completed

Helicobacter Pylori Sample Collection Protocol Post Therapy Subjects

Nausea | Abdominal Pain | Weight Loss | Helicobacter Pylori Infection | Gastric Ulcer | Stomach Ulcer | Loss of Appetite | Bloating

United States, Italy
Calanus
Biofortis Clinical Research, Inc.

Completed

Study to Evaluate the Acute Bioavailability of EPA and DHA From a DietarySupplement in Healthy Men and Women

Healthy

United States
Suneva Medical, Inc.
ethica Clinical Research Inc.

Completed

The Use of Bellafill for Atrophic Acne Scar Correction in the Full Facial Area

Atrophic Acne Scarring

United States
Thync Global, Inc.
ethica Clinical Research Inc.

Completed

12-Week Study Assessing Change in Psoriasis Severity and Level of Stress Using TEN

Stress | Psoriasis

United States
Scarless Laboratories, Inc.
ethica Clinical Research Inc.

Completed

Safety and Efficacy of SLI-F06 in Wound Healing and Scar Appearance

Scars

United States
CAGE Bio Inc.
ethica Clinical Research Inc.

Completed

CGB-400 for the Reduction of Facial Redness and Bumps and Blemishes

Rosacea

United States
CAGE Bio Inc.
ethica Clinical Research Inc.

Completed

CGB-400 for the Reduction of Facial Redness

Rosacea

United States
Thync Global, Inc.
ethica Clinical Research Inc.

Unknown

Efficacy and Safety Study of Autonomic Nerve Modulation (ANM) in Subjects With Moderate Plaque Psoriasis

Plaque Psoriasis

United States
CAGE Bio Inc.
ethica Clinical Research Inc.

Completed

CGB-400 Topical Gel for the Treatment of Inflammatory Lesions of Rosacea

Rosacea

United States
Suneva Medical, Inc.
ethica Clinical Research Inc.

Completed

Use of Artefill® for Moderate to Severe Atrophic Acne Scar Correction

Atrophic Acne Scar

United States
Suneva Medical, Inc.
ethica Clinical Research Inc.

Completed

A Pilot Study to Evaluate the Safety and Effectiveness of Microneedling and Bellafill to Treat Facial Acne Scars

Atrophic Acne Scars

United States
Akros Pharma Inc.
ICON Clinical Research

Recruiting

Evaluate Efficacy, Safety and Tolerability of JTT-861 in Subjects With Heart Failure With Reduced Ejection Fraction (POWER-HF)

Chronic Heart Failure

United States
Clinical Research Consultants, Inc.
HumanOptics AG

Recruiting

Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects

Full Aniridia | Partial Aniridia

United States
Amytrx Therapeutics, Inc.
Amarex Clinical Research

Completed

Topically Applied AMTX-100 CF for Adult Patients With Mild to Moderate Atopic Dermatitis

Atopic Dermatitis

United States
Medline Industries
Rochester Clinical Research, Inc.

Completed

Wetness Sensing System

System Validation

United States
J3 Bioscience, Inc.
Advanced Clinical Research

Completed

Efficacy of VR101 as a Personal Lubricant

Sexual Dysfunction, Physiological

United States
Trevena Inc.
Lotus Clinical Research, LLC

Completed

A Study of TRV130 for the Treatment of Pain After Abdominoplasty

Pain

United States
Teoxane SA
ethica Clinical Research Inc.

Completed

TEOSYAL® RHA Ultra Deep and Perlane-L® for the Correction of Nasolabial Folds

Nasolabial Folds, Wrinkles

United States
HeartFlow, Inc.
Duke Clinical Research Institute

Completed

The PLATFORM Study: Prospective LongitudinAl Trial of FFRct: Outcome and Resource IMpacts) (PLATFORM)

Coronary Artery Disease

United States, Germany, United Kingdom, Denmark, Belgium, Austria, France, Italy
Virginia Clinical Research, Inc.
Celgene Corporation

Unknown

Pilot Study of Apremilast (CC-10004) in the Treatment of Moderate to Severe Lichen Planus

Lichen Planus

United States
Artivion Inc.
Duke Clinical Research Institute

Terminated

PROACT Xa - A Trial to Determine if Participants With an On-X Aortic Valve Can be Maintained Safely on Apixaban

Aortic Valve Stenosis | Aortic Valve Disease | Aortic Valve Failure

United States

Clinical Trials Sponsored by Omnispec clinical research Inc

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Dominican Republic

Conditions

Rare Diseases

Drug Interventions

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