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Last Updated: April 26, 2024

CLINICAL TRIALS PROFILE FOR MENADIONE


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All Clinical Trials for menadione

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00656786 ↗ Safety, Tolerability and Systemic Absorption of Menadione Topical Lotion for Epidermal-Growth-Factor-Receptor (EGFR) Inhibitor-Associated Rash Completed Spectrum Pharmaceuticals, Inc Phase 1 2008-04-03 This is a clinical research study of an experimental new medication, Menadione Topical Lotion (MTL). The study lotion is experimental and has not been approved for public use. Hana Biosciences, Inc., the company that is developing MTL, is the sponsor of this study. EGFR inhibitors are used to treat non-small cell lung cancer (NSCLC), pancreatic cancer, colorectal cancer, breast cancer and head and neck cancer. One of the side effects of EFGR inhibitors is skin toxicities including an acneform skin rash. This study is a Phase 1 study. The main purposes of this study are: - Evaluate the safety and tolerability of Menadione Topical Lotion as an emergent and pre-emergent treatment for EGFR inhibitor-associated rash - Evaluate the systemic absorption and bioavailability of Menadione Topical Lotion as an emergent and pre-emergent treatment for EGFR inhibitor-associated rash It is planned that up to 24 patients undergoing EGFR inhibitor therapy will take part in this study at multiple clinical centers.
NCT01393821 ↗ Menadione Topical Lotion in Treating Skin Discomfort and Psychological Distress in Patients With Cancer Receiving Panitumumab, Erlotinib Hydrochloride, or Cetuximab Active, not recruiting Mayo Clinic N/A 2012-01-01 This clinical trial studies menadione topical lotion in treating skin discomfort and psychological distress in patients with cancer receiving panitumumab, erlotinib hydrochloride, or cetuximab. Menadione topical lotion may prevent rash or other skin discomfort and help alleviate psychological distress and pain in patients receiving treatment with panitumumab, erlotinib hydrochloride, or cetuximab
NCT02880033 ↗ Oxidative Stress and Apoptosis of Energy Metabolism by Deferiprone From the Circulating Lymphocytes Completed University Hospital, Lille N/A 2011-02-01 Peripheral blood mononuclear cells (PBMC) and platelets could be interesting ex vivo models to study brain diseases. Indeed, there is no access to neurons from patients. However, PBMC can exhibit different physiopathological mechanisms that are ubiquitous (i.e. oxidative stress, mitochondriopathy with energy metabolism, inflammation, protein folding, iron metabolism and programmed cell death ...). The platelets are pivotal in the healing system with large range of growth factors. A new therapeutic concept of conservative iron chelation with deferiprone for neuroprotection is under development. The action of deferiprone on the different mechanisms and notably the oxidative stress are to obtain from a collection of PBMC and platelets from patient having Parkinson's disease and Amyotrophic lateral sclerosis and healthy controls to study ex vivo. PBMC and platelets will be stored for future analyses.
NCT04705714 ↗ Antibacterial and Anti-biofilm Activity of Frankincense Extract Against Porphyromonas Gingivalis Completed Tanta University Phase 1 2021-01-15 Boswellia sacra Flueck. oleoresin extract (frankincense) was traditionally used in the treatment of different diseases as respiratory, rheumatoid arthritis, and bacterial infections. Therefore, the antibacterial and antibiofilm activity of frankincense extract against Porphyromonas gingivalis periodontal pathogen clinical isolates were studied
NCT05417880 ↗ Vitamin D, K2 Plus Empagliflozin Combination in Type Two Diabetes Mellitus Not yet recruiting University of Health Sciences Lahore Phase 3 2022-08-01 The main purpose of the VETA trial is to verify the potential beneficial effects of the combination of micronutrients namely Vitamin D3 and K2 in combination with oral antihyperglycemic Empagliflozin in Diabetes Mellitus
NCT05417880 ↗ Vitamin D, K2 Plus Empagliflozin Combination in Type Two Diabetes Mellitus Not yet recruiting Scotmann Pharmaceuticals Phase 3 2022-08-01 The main purpose of the VETA trial is to verify the potential beneficial effects of the combination of micronutrients namely Vitamin D3 and K2 in combination with oral antihyperglycemic Empagliflozin in Diabetes Mellitus
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for menadione

Condition Name

Condition Name for menadione
Intervention Trials
Oxidative Stress 1
Pain 1
Parkinson's Disease 1
Periodontal Diseases 1
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Condition MeSH

Condition MeSH for menadione
Intervention Trials
Motor Neuron Disease 1
Iron Overload 1
Amyotrophic Lateral Sclerosis 1
Diabetes Mellitus 1
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Clinical Trial Locations for menadione

Trials by Country

Trials by Country for menadione
Location Trials
United States 8
France 1
Canada 1
Pakistan 1
Egypt 1
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Trials by US State

Trials by US State for menadione
Location Trials
Minnesota 1
Arizona 1
Texas 1
Pennsylvania 1
Missouri 1
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Clinical Trial Progress for menadione

Clinical Trial Phase

Clinical Trial Phase for menadione
Clinical Trial Phase Trials
Phase 3 1
Phase 1 2
N/A 2
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Clinical Trial Status

Clinical Trial Status for menadione
Clinical Trial Phase Trials
Completed 3
Active, not recruiting 1
Not yet recruiting 1
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Clinical Trial Sponsors for menadione

Sponsor Name

Sponsor Name for menadione
Sponsor Trials
Tanta University 1
University of Health Sciences Lahore 1
Scotmann Pharmaceuticals 1
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Sponsor Type

Sponsor Type for menadione
Sponsor Trials
Other 4
Industry 2
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