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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04946383
Other study ID # IHB-QD-001
Secondary ID
Status Active, not recruiting
Phase Phase 2
First received
Last updated
Start date December 16, 2020
Est. completion date June 30, 2022

Study information

Verified date August 2021
Source TruDiagnostic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessing the effects of Quercitin and Dasatinib over a 16 week period on participatns' epigenetic biological aging. The patients are being tested at baseline, halfway point, and after the trial period.


Description:

This is a prospective non-randomized clinical study of 20-25 patients to evaluate the effectiveness of Quercetin and Dasatinib supplements on the patient's epigenetic aging rate. The investigators predict that Quercetin and Dasatinib combined will slow cell proliferation and thus decelerate the rate of aging. There is evidence that Quercetin and Dasatinib slows cell proliferation and decelerates aging and the risk of age-related diseases. The aim of this pilot study is to evaluate the safety, efficacy and feasibility of Quercetin and Dasatinib as an effective treatment option to improve clinical care of healthy individual's epigenetic aging rate thus prolonging longevity. Despite considerable effort, successful treatment of reversing one's biological age has been shown to be a difficult therapeutic challenge. There is evidence that Dasatinib+Quercetin(Quercetin and Dasatinib) is a safe and effective treatment option to improve clinical care of healthy individual's biological age. Studies have shown that Dasatinib+Quercetin slows cell proliferation and decelerates aging and the risk of age-related diseases.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 25
Est. completion date June 30, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - Men and women - Ages 40 and older - Patient must be able to comply with treatment plan and laboratory tests Exclusion Criteria: - Neoplastic cancer within 5 years prior to screening, except for cutaneous basal cell or squamous cell cancer resolved by excision - No immune system issues or immunodeficiency disease - No history of viral illness which could be reactivated by immune down regulation - Presence of clinically significant acute or unstable cardiovascular and cerebrovascular (stroke) - Diagnosis of a transient ischemic attack in the 6 months prior to screening - Patients infected with hepatitis, C or HIV - Patients with Body Mass Index (BMI) > 40 kg/m2 - Presence of active infection 9. Any other illness, psychiatric disorder, alcohol or chemical dependence that in the opinion of the investigator would render a patient unsuitable to participate in the study - Unable or unwilling to provide required blood sample for testing - As for the male-participants they are recommended to avoid fertilization for the first 6 months after the clinical trial. - If the patient has previously used Quercetin and Dasatinib.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dasatinib plus Quercetin
Dasatinib plus Quercetin

Locations

Country Name City State
United States The Institute for Hormonal Balance Orlando Florida

Sponsors (1)

Lead Sponsor Collaborator
TruDiagnostic

Country where clinical trial is conducted

United States, 

References & Publications (3)

Cavalcante MB, Saccon TD, Nunes ADC, Kirkland JL, Tchkonia T, Schneider A, Masternak MM. Dasatinib plus quercetin prevents uterine age-related dysfunction and fibrosis in mice. Aging (Albany NY). 2020 Jan 18;12(3):2711-2722. doi: 10.18632/aging.102772. Epub 2020 Jan 18. — View Citation

Ermogenous C, Green C, Jackson T, Ferguson M, Lord JM. Treating age-related multimorbidity: the drug discovery challenge. Drug Discov Today. 2020 Aug;25(8):1403-1415. doi: 10.1016/j.drudis.2020.06.016. Epub 2020 Jun 20. Review. — View Citation

Hickson LJ, Langhi Prata LGP, Bobart SA, Evans TK, Giorgadze N, Hashmi SK, Herrmann SM, Jensen MD, Jia Q, Jordan KL, Kellogg TA, Khosla S, Koerber DM, Lagnado AB, Lawson DK, LeBrasseur NK, Lerman LO, McDonald KM, McKenzie TJ, Passos JF, Pignolo RJ, Pirtskhalava T, Saadiq IM, Schaefer KK, Textor SC, Victorelli SG, Volkman TL, Xue A, Wentworth MA, Wissler Gerdes EO, Zhu Y, Tchkonia T, Kirkland JL. Senolytics decrease senescent cells in humans: Preliminary report from a clinical trial of Dasatinib plus Quercetin in individuals with diabetic kidney disease. EBioMedicine. 2019 Sep;47:446-456. doi: 10.1016/j.ebiom.2019.08.069. Epub 2019 Sep 18. Erratum in: EBioMedicine. 2020 Feb;52:102595. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Epigenetic Age Test Change from baseline to 6 months
Secondary Examining Methylation changes Methylation analysis via the Illumina 850k epic array. Methylation will be assessed at 850,000 spots on the DNA, these are located on CpG sites. These are the spots on DNA that have cytosine and guanine right next to each other. Change from baseline to 6 months
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