Search clinical trials for: loratadine (Clarityne [Reference Treatment])

Total 89 results

Xian-Janssen Pharmaceutical Ltd.

Completed

A Study to Assess the Bioequivalence of Xisimin (Loratadine) Tablets Under Fasting and Fed Conditions in Healthy Participants Compared With Clarityne Tablets

Healthy

China
Xian-Janssen Pharmaceutical Ltd.

Completed

A Study to Assess the Relative Bioavailability of Xisimin (Loratadine) Tablets Under Fasting and Fed Conditions in Healthy Participants Compared to Clarityne Tablets

Healthy

Taiwan
Bayer

Completed

To Assess Bioequivalence of Loratadine Oral Solution/Syrup Versus Claritin Peach Syrup (Bordeaux)

Histamine H1 Antagonists, Non-Sedating

Germany
Otsuka Australia Pharmaceutical Pty Ltd

Completed

Refine and Assess the Readability of Patient, Carer, and Clinician Treatment Preference in Myelodysplasia Questionnaire (TPMQ)

Myelodysplastic Syndrome (MDS)

Australia
Sandoz

Completed

To Demonstrate the Relative Bioavailability Study of Loratadine 10 mg Tablets

Allergy
Assistance Publique - Hôpitaux de Paris
University Hospital, Clermont-Ferrand; Rennes University Hospital; Nantes University...

Unknown

Pulpotomy vs Pulpectomy Outcome. (PULPSAVE)

Inflammatory Pulp Diseases Related to Carious Teeth

France
Chiesi Farmaceutici S.p.A.
Quintiles, Inc.

Completed

Pharmacokinetic Interaction and the Safety of Inhaled CHF5259 and CHF6001

Copd

United Kingdom
Merck Sharp & Dohme LLC

Completed

Observation of Use of Claritin (Loratadine) Tablet, RediTabs, and Dry Syrup in Children (Study P05834)(COMPLETED)

Rhinitis, Allergic, Perennial | Rhinitis, Allergic, Seasonal | Pruritus | Urticaria
Bayer

Completed

A Study to Evaluate Cooling Sensation of an Allergy Product in Adults With a History of Allergies

Allergic Rhinitis

United States
Merck Sharp & Dohme LLC

Completed

Post Approval Pharmacokinetic Study of Loratadine in Japanese Pediatric and Adult Patients (Study P05539)

Perennial Allergic Rhinitis
Pamukkale University

Completed

Treatment Preferences in Patients With Low Back Pain

Low Back Pain

Turkey
University Children's Hospital Basel
Permamed AG, Switzerland; Galvita AG, Switzerland

Completed

Bioequivalence of a Single-dose of 12 mg IVERMECTIN as Orally Disintegrating Mini Tablets Versus a Single-dose of 12 mg Regular IVERMECTIN Tablets in Healthy Adults Under Fasting Conditions (CHILD-IVITAB)

Bioequivalence

Switzerland
ALK-Abelló A/S

Completed

Efficacy and Safety of Grass Sublingual Tablet in Children and Adolescents (P05239 AM3)(COMPLETED)

Allergy | Rhinitis | Conjunctivitis | Rhinoconjunctivitis
Merck KGaA, Darmstadt, Germany

Completed

Relative Bioavailability of Two Tepotinib Film-Coated Tablet Formulations in Healthy Volunteers

Healthy

Germany
Janssen Infectious Diseases BVBA

Completed

A Study to Assess the Relative Bioavailability of TMC207 Following Single-Dose Administrations of Two Pediatric Formulations in Healthy Adult Participants

Healthy | Biological Availability

Netherlands
Thammasat University

Completed

Benjakul Extract and Loratadine for Treatment Allergic Rhinitis Patients

Allergic Rhinitis

Thailand
Bayer

Completed

A Manufacturing Transfer Study Comparing the Bioequivalence of a Single Oral Dose of Claritin-D 12-Hour Extended Release Tablet From 2 Different Manufacturers Under Fasted Conditions in Healthy Adult Subjects

Clinical Pharmacology

United States
GlaxoSmithKline

Completed

To Assess the Mildness of a Cosmetic Cleanser in Healthy Participants Using the Forearm-Controlled Application Technique (FCAT)

Skin Care

Brazil
University of Utah

Completed

Improving Decision Role Concordance in Newly Diagnosed Breast Cancer Patients

Breast Cancer
Bayer

Completed

A Manufacturing Transfer Study Comparing the Bioequivalence of a Single Oral Dose of Claritin-D 12-Hour Extended Release Tablet From 2 Different Manufactuers Under Fed Conditions in Healthy Adult Subjects

Clinical Pharmacology

United States
CEN Biotech
medi

Completed

Circaid® Compression Sleeve Versus Short-stretching Bandage in Upper Limb Lymphatic Edema

Lymphedema of Upper Arm

France
Andover Research Eye Institute

Completed

A Study Comparing the Efficacy of Pataday® Once Daily Relief Extra Strength to Claritin® Tablets 24-Hour in Subjects With Allergic Conjunctivitis

Allergic Conjunctivitis

United States
Shenzhen TargetRx, Inc.
First Affiliated Hospital Bengbu Medical College

Completed

TGRX-326 Phase I/II Pharmacokinetic Study

Non Small Cell Lung Cancer

China
Thai Traditional Medical Knowledge Fund
Thammasat University

Completed

Study of Efficacy and Safety of Ginger Extract Compared With Loratadine for Treatment of Allergic Rhinitis

Rhinitis,Allergic

Thailand
Peking Union Medical College Hospital

Unknown

Effectiveness of Qufeng Shengshi Fang on Treatment of Allergic Rhinitis.

Rhinitis, Allergic, Perennial

China
Janssen Research & Development, LLC

Completed

A Crossover Study to Evaluate the Bioavailability of Ibrutinib Suspension and Sprinkle Formulations Compared to Capsules in Healthy Adults

Healthy

Belgium
Wake Forest University Health Sciences

Completed

Evaluation of Loratadine for G-CSF Induced Bone Pain in Patients With Hematologic Malignancies

Lymphoma | Leukemia

United States
Janssen Research & Development, LLC
Pharmacyclics LLC.

Completed

A Study to Assess the Absolute Bioavailability of Oral PCI-32765 and the Effect of Grapefruit Juice on the Bioavailability of PCI-32765 in Healthy Participants

Healthy Volunteer

Belgium
University of Vermont
Cancer and Leukemia Group B

Unknown

Evaluation of Loratadine for Prevention of Pegfilgrastim-Induced Pain

Pegfilgrastim-induced Back and Leg Pain

United States
University of Michigan

Terminated

Loratadine for Improvement of Bone Pain in Patients With Chronic Granulocyte-Colony Stimulating Factor (G-CSF) Use

Bone Pain

United States
Artromedical Konrad Malinowski Clinic

Recruiting

Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment

Meniscus; Degeneration | Meniscus Lesion | Meniscus Tear | Meniscus Disorder

Poland
University of Chicago

Completed

The Efficacy of Claritin in Healthy Subjects

Healthy

United States
ALK-Abelló A/S

Completed

Efficacy and Safety of Grass Sublingual Tablet in Adults (P05238 AM3)(COMPLETED)

Allergy | Rhinitis | Conjunctivitis | Rhinoconjunctivitis
Universidade do Sul de Santa Catarina

Completed

Quality of Life in Patients With Allergic Rhinitis: Clinical Trial With Bilastine or Loratadine (QolRhinitis)

Allergic Rhinitis
Amicus Therapeutics France SAS

Active, not recruiting

Treatment-related Benefit and Satisfaction in Fabry Patients. Insight in Patients Expectations and Preferences

Fabry Disease | Anderson Fabry Disease

France
AstraZeneca

Completed

A Study to Assess the Reaction of Body for Four Different Formulations of AZD9977 (Part A) and Influence of Food and Lower Dose of a Selected Formulation (Part B) in Healthy Male Subjects

Heart Failure

United Kingdom
Johnson & Johnson Consumer and Personal Products...
Pfizer

Completed

Randomized, Double Blind, Parallel Group, Placebo Controlled, Multi-Center Study of the Efficacy and Safety of Cetirizine HCl Syrup vs. Loratadine Syrup vs. Placebo in Treatment of Children With Seasonal Allergic Rhinitis (SAR)

Allergic Rhinitis | Rhinitis, Allergic, Seasonal | Hay Fever | SAR
Janssen Research & Development, LLC

Completed

A Study to Evaluate Bioequivalence and Adhesion of a Transdermal Contraceptive Patch Manufactured With Newly Sourced Adhesive Components and Currently Marketed EVRA in Healthy Adult Women

Healthy

Belgium
H. Lundbeck A/S

Completed

Comparative Study of the Pharmacokinetics and Bioequivalence of Two Flupentixol Formulations

Bioequivalence Study in Healthy Subjects

Russian Federation
Cerevel Therapeutics, LLC

Recruiting

A Study Evaluating the Pharmacokinetics and Relative Bioavailability of Emraclidine Immediate-Release Tablets in Healthy Adult Participants

Healthy Participants

United States
Jiangxi University of Traditional Chinese Medicine

Active, not recruiting

A Randomized Patient Preference Trial on Heat-sensitive Moxibustion for Primary Hypertension in Community

Primary Hypertension

China
Rutgers, The State University of New Jersey
National Cancer Institute (NCI)

Recruiting

Loratadine for the Reduction of G-CSF Induced Bone Pain in Patients With Multiple Myeloma Undergoing Stem Cell Mobilization

Plasma Cell Myeloma

United States
Janssen Research & Development, LLC

Completed

A Study of New Transdermal Contraceptive Patch at End of Shelf Life and Currently Marketed EVRA at the Beginning of Shelf Life in Healthy Women

Healthy

Netherlands, Germany, Belgium
Sanofi

Completed

Study of Triamcinolone Acetonide on the Growth Velocity of Children, Ages 3 to 9, With Perennial Allergic Rhinitis (PAR)

Rhinitis, Allergic, Perennial

United States
AstraZeneca
Parexel

Completed

A Study to Assess the Amount of Drug Levels in Blood and Safety of AZD5718 Formulations in Healthy Volunteers

Coronary Artery Disease (CAD)

United Kingdom
University Hospital, Clermont-Ferrand

Completed

Levobupivacaine for Epidural Analgesia in Labour

Analgesia, Epidural
Ukrainian Medical Stomatological Academy

Completed

Effects of Azithromycin as an Adjunct to Scaling and Root Planning in the Treatment of Periodontitis

Periodontitis

Ukraine
Columbia University
National Heart, Lung, and Blood Institute (NHLBI)

Completed

COPES Phase I Randomized Controlled Trial of Treatment For Distress in Heart Disease Patients

Depression | Heart Diseases

United States
University Hospital, Brest

Completed

Stress Factors Induced by Patient and Young Clinicien During Endodontic Treatment (STRESSENDO)

Endodontic Treatment

France
Janssen-Cilag, S.A.

Completed

A Study to Assess the Clinical Profile of Patients in Spain With Moderate to Severe Psoriasis.

Psoriasis

3

Subscribe