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topic_facet:"Phase: Phase 1"
topic_facet:"Medical Condition: Healthy Volunteers"
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PubPharm (1.013)
1
A Bioequivalence study of single dose, two-way crossover design with two-period, two-treatment of Octreotide-SBS 100 mcg/mL subcutaneous injection relative to Sandostatin® : A Bioequivalence study of single dose, two-way crossover design with two-period, two-treatment of Octreotide-SBS 100 mcg/mL subcutaneous injection relative to Sandostatin®
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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2
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover of Enoxaparin-SBS pre-filled injection 80 mg/0.8 mL subcutaneous injection relative to Clexane® pre-filled injection 80 mg/0.8 mL in healthy Thai volunteers : A Bioequivalence study of a randomized, open-label, single dose, two-way crossover of Enoxaparin-SBS pre-filled injection 8000 anti-Xa IU (80 mg)/0.8 mL subcutaneous injection relative to Clexane® pre-filled injection 8000 anti-Xa IU (80 mg)/0.8 mL
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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3
A Pivotal In Vivo Bioequivalence Study for Topical Mometasone Furoate 0.1 % Cream, Elomet® and MODASONE CREAM, in Healthy Thai Volunteers Based on Vasoconstriction in the Microvasculature of the Skin : A Pivotal In Vivo Bioequivalence Study for Topical Mometasone Furoate 0.1 % Cream, Elomet® and MODASONE CREAM, in Healthy Thai Volunteers Based on Vasoconstriction in the Microvasculature of the Skin
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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4
A Bioequivalence study of single dose, two-way crossover design with two-period, two-treatment of Octreotide-SBS 100 mcg/mL subcutaneous injection relative to Sandostatin® : A Bioequivalence study of single dose, two-way crossover design with two-period, two-treatment of Octreotide-SBS 100 mcg/mL subcutaneous injection relative to Sandostatin®
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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5
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover of Enoxaparin-SBS pre-filled injection 80 mg/0.8 mL subcutaneous injection relative to Clexane® pre-filled injection 80 mg/0.8 mL in healthy Thai volunteers : A Bioequivalence study of a randomized, open-label, single dose, two-way crossover of Enoxaparin-SBS pre-filled injection 8000 anti-Xa IU (80 mg)/0.8 mL subcutaneous injection relative to Clexane® pre-filled injection 8000 anti-Xa IU (80 mg)/0.8 mL
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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6
A Pivotal In Vivo Bioequivalence Study for Topical Mometasone Furoate 0.1 % Cream, Elomet® and MODASONE CREAM, in Healthy Thai Volunteers Based on Vasoconstriction in the Microvasculature of the Skin : A Pivotal In Vivo Bioequivalence Study for Topical Mometasone Furoate 0.1 % Cream, Elomet® and MODASONE CREAM, in Healthy Thai Volunteers Based on Vasoconstriction in the Microvasculature of the Skin
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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7
Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of CC-99677 in Healthy Adult Japanese Participants. : A Phase 1 Evaluation of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of CC 99677 in Healthy Adult Japanese Subjects
enthalten in:
ClinicalTrials.gov
| 2022
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8
Safety, Tolerability and Pharmacokinetics of XW10508 Immediate and Modified Release Formulations in Healthy Adults : A Phase 1 Study to Assess the Safety, Tolerability and Pharmacokinetics of XW10508 Immediate and Modified Release Formulations in Healthy Adults
enthalten in:
ClinicalTrials.gov
| 2022
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9
A Study to Assess the Relative Bioavailability and Safety of Different Formulations of AZD4831 in Fasted State in Healthy Volunteers. : A Randomized, Single-dose, Open-label, Single-center, Crossover Study to Assess the Relative Bioavailability and Safety of Different Formulations of AZD4831 in Fasted State in Healthy Volunteers.
enthalten in:
ClinicalTrials.gov
| 2022
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10
A Study to Determine the Safety of AV-1, an Antibody Being Developed for Treatment of Dengue, in Healthy Volunteers : A Phase 1a, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Determine the Safety and Pharmacokinetics of AV-1 in Healthy Male and Female Adult Subjects
enthalten in:
ClinicalTrials.gov
| 2022
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Thema: Phase: Phase 1
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Thema: Medical Condition: Healthy Volunteers
Medienart
1.013
Aufsätze
1.013
E-Artikel
1.013
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Zeitschriftentitel
999
ClinicalTrials.gov
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WHO International Clinical Trials Registry Plat...
Thema
1.013
610
Medical Condition: Healthy Volunteers
Phase: Phase 1
1.013
Study Type: Interventional
918
Recruitment Status: Completed
40
Recruitment Status: Terminated
13
Recruitment Status: Not yet recruiting
13
Recruitment Status: Recruiting
13
Recruitment Status: Unknown status
12
Recruitment Status: Withdrawn
5
Respiratory Aspiration
4
Malnutrition
3
Marijuana Abuse
3
Recruitment Status: Active, not recruiting
2
Crush Injuries
2
Hypoxia
2
Overweight
1
Aneurysm
1
Cognitive Dysfunction
1
Dilatation, Pathologic
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Erscheinungszeitraum
381
2020-
603
2010-2019
29
2000-2009
Erscheinungsjahr(e)
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Sprache
1.013
Englisch
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