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Last Updated: December 22, 2024

CLINICAL TRIALS PROFILE FOR LINCOMYCIN HYDROCHLORIDE


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All Clinical Trials for lincomycin hydrochloride

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01058824 ↗ Relative Bioavailability Study Of Two Lincomycin Hydrochloride Hard Gelatinous Capsule Completed Pfizer Phase 1 2009-04-01 To assess the relative bioavailability of two different batches of Frademicina® drug product, containing 500 mg lincomycin hydrocloride, manufactured by Pfizer Laboratories Ltd. The formulations' comparative bioavailability after oral administration will be assessed based on the statistical comparisons of the relevant pharmacokinetic parameters, obtained from the drug concentrations in the blood. The lincomycin hydrocloride concentration will be measured by a proper and validated analytical method.
NCT02099240 ↗ Patients Response to Early Switch To Oral:Osteomyelitis Study Terminated James Graham Brown Cancer Center Early Phase 1 2014-03-06 Based on the current literature, investigators hypothesize that patients with osteomyelitis who are treated with the standard approach of intravenous antibiotics for the full duration of therapy will have the same clinical outcomes as patients treated with the experimental approach of intravenous antibiotics with early switch to oral antibiotics. The primary objective of this study is to compare patients with osteomyelitis treated with the standard approach of intravenous antibiotics for the full duration of therapy versus patients treated with intravenous antibiotics with an early switch to oral antibiotics in relation to clinical outcomes at 12 months after discontinuation of antibiotic therapy. Secondary objectives of the study include the evaluation of adverse events related to the use of antibiotics as well as the cost of care evaluated from the hospital perspective.
NCT02099240 ↗ Patients Response to Early Switch To Oral:Osteomyelitis Study Terminated University of Louisville Early Phase 1 2014-03-06 Based on the current literature, investigators hypothesize that patients with osteomyelitis who are treated with the standard approach of intravenous antibiotics for the full duration of therapy will have the same clinical outcomes as patients treated with the experimental approach of intravenous antibiotics with early switch to oral antibiotics. The primary objective of this study is to compare patients with osteomyelitis treated with the standard approach of intravenous antibiotics for the full duration of therapy versus patients treated with intravenous antibiotics with an early switch to oral antibiotics in relation to clinical outcomes at 12 months after discontinuation of antibiotic therapy. Secondary objectives of the study include the evaluation of adverse events related to the use of antibiotics as well as the cost of care evaluated from the hospital perspective.
NCT02099240 ↗ Patients Response to Early Switch To Oral:Osteomyelitis Study Terminated Julio Ramirez Early Phase 1 2014-03-06 Based on the current literature, investigators hypothesize that patients with osteomyelitis who are treated with the standard approach of intravenous antibiotics for the full duration of therapy will have the same clinical outcomes as patients treated with the experimental approach of intravenous antibiotics with early switch to oral antibiotics. The primary objective of this study is to compare patients with osteomyelitis treated with the standard approach of intravenous antibiotics for the full duration of therapy versus patients treated with intravenous antibiotics with an early switch to oral antibiotics in relation to clinical outcomes at 12 months after discontinuation of antibiotic therapy. Secondary objectives of the study include the evaluation of adverse events related to the use of antibiotics as well as the cost of care evaluated from the hospital perspective.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for lincomycin hydrochloride

Condition Name

Condition Name for lincomycin hydrochloride
Intervention Trials
Bacterial Infections 1
Osteomyelitis 1
Staphylococcus Aureus Bacteremia 1
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Condition MeSH

Condition MeSH for lincomycin hydrochloride
Intervention Trials
Staphylococcal Infections 1
Bacteremia 1
Osteomyelitis 1
Bacterial Infections 1
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Clinical Trial Locations for lincomycin hydrochloride

Trials by Country

Trials by Country for lincomycin hydrochloride
Location Trials
Australia 9
New Zealand 7
Canada 6
Brazil 1
Israel 1
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Trials by US State

Trials by US State for lincomycin hydrochloride
Location Trials
Kentucky 1
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Clinical Trial Progress for lincomycin hydrochloride

Clinical Trial Phase

Clinical Trial Phase for lincomycin hydrochloride
Clinical Trial Phase Trials
Phase 4 1
Phase 1 1
Early Phase 1 1
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Clinical Trial Status

Clinical Trial Status for lincomycin hydrochloride
Clinical Trial Phase Trials
Completed 1
Not yet recruiting 1
Terminated 1
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Clinical Trial Sponsors for lincomycin hydrochloride

Sponsor Name

Sponsor Name for lincomycin hydrochloride
Sponsor Trials
Menzies School of Health Research 1
Queensland University of Technology 1
Sunnybrook Health Sciences Centre 1
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Sponsor Type

Sponsor Type for lincomycin hydrochloride
Sponsor Trials
Other 12
Industry 1
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