Topical-RAPA Use in Inflammation Reversal and Re-setting the Epigenetic Clock
NCT04608448 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 22
Last updated 2023-07-19
Summary
Topical Rapamycin ointment will be applied to participant forearms to test whether epigenetic changes in the skin are elicited.
Conditions
- Aging
- Epigenetics
- Inflammatory Mediators
Interventions
- DRUG
-
Rapamycin Topical Ointment
8% topical rapamycin ointment
- OTHER
-
Placebo
Petrolatum ointment containing no active ingredient
Sponsors & Collaborators
-
National Institute on Aging (NIA)
collaborator NIH -
The University of Texas Health Science Center at San Antonio
lead OTHER
Principal Investigators
-
Ellen Kraig, PhD · University of Texas Health at San Antonio
-
Dean L Kellogg, Jr., MD, PhD · University of Texas Health at San Antonio
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 65 Years
- Max Age
- 95 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-04-28
- Primary Completion
- 2022-04-15
- Completion
- 2022-04-15
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
The Effect of Naproxen on the Pharmacokinetic Profile of LC350189 in Healthy Adults
NCT04139824 ·Status: COMPLETED ·Phase: PHASE1
-
Oral Bioequivalence Study of PL 3100 and Naproxen in Healthy Adults
NCT00966641 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Pharmacokinetic Trial of Naproxen Sodium and Diphenhydramine Hydrochloride Soft Capsules Versus Naproxen Sodium and Diphenhydramine Hydrochloride Tablets in Healthy Adult Subjects Under Fed Conditions
NCT03424135 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Bioavailability Study of Naproxen Delayed-Release Tablets (375 mg)
NCT00959439 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Learn About Whether BAY H006689 Causes an Allergic Reaction When Applied as a Topical Gel in Healthy Participants
NCT06415019 ·Status: COMPLETED ·Phase: PHASE1
-
Effectiveness of Theramine on Chronic Back Pain
NCT01468025 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Learn About Whether BAYH006689 Causes Skin Irritation When Applied as a Topical Gel in Healthy Participants
NCT06511973 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate the Pharmacokinetic Profile of ALXN2050 Modified Release Prototype Formulations and Immediate Release Reference Tablet in Healthy Adult Participants
NCT05780645 ·Status: COMPLETED ·Phase: PHASE1
-
Naproxen in Preventing DNA Mismatch Repair Deficient Colorectal Cancer in Patients With Lynch Syndrome
NCT02052908 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics Study Comparing Naproxen Sodium Extended Release and Naprelan
NCT00969449 ·Status: COMPLETED ·Phase: PHASE1
-
Study Evaluating the Bioavailability of Naproxen 375 mg in Two Formulations
NCT00692055 ·Status: COMPLETED ·Phase: PHASE1
-
Actual Use Trial of Naproxen Sodium
NCT01427803 ·Status: COMPLETED ·Phase: PHASE3
-
A Pharmacokinetic (PK) Study Evaluating Naproxen and Esomeprazole Plasma Levels
NCT00749385 ·Status: COMPLETED ·Phase: PHASE1
-
Phase I Study to Evaluate Bioavailability of Naproxen as PN400 Compared to Naproxen as Naprosyn E
NCT00907400 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase 1 Study to Compare the PK and Safety of Naproxcinod in Hepatic Impaired Patients and Matching Healthy Subjects
NCT00621881 ·Status: COMPLETED ·Phase: PHASE1
-
A Pharmacokinetic Trial of Naproxen Sodium and Diphenhydramine Hydrochloride Soft Capsules Versus Naproxen Sodium and Diphenhydramine Hydrochloride Tablets in Healthy Adult Subjects
NCT03396250 ·Status: COMPLETED ·Phase: PHASE1
-
Naproxen Sodium ER Pharmacokinetic Study
NCT00818415 ·Status: COMPLETED ·Phase: PHASE1
-
Study Evaluating the Effect of Food on the Bioavailability of PN400 Components
NCT00676442 ·Status: COMPLETED ·Phase: PHASE1
-
Phase I Study on Multiple Oral Dosing of CG100649
NCT01154790 ·Status: COMPLETED ·Phase: PHASE1
-
A Comparative Bioavailability and Pharmacokinetic Study of TNX-102 2.4 mg and Cyclobenzaprine 5 mg Tablets in Healthy Adults.
NCT01490788 ·Status: COMPLETED ·Phase: PHASE1
-
Phase I Study to Evaluate Bioavailability of Naproxen as PN400 Compared to Naproxen as Proxen S and Naprosyn E
NCT00761501 ·Status: COMPLETED ·Phase: PHASE1
-
Naproxen Sodium Extended-Release Actual Use Study
NCT00751400 ·Status: COMPLETED ·Phase: PHASE3
-
To Assess the Effect of Naproxcinod Versus Naproxen and Ibuprofen on Arterial Blood Pressure in Osteoarthritis Patients With Controlled Essential Hypertension
NCT00662896 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Effect of Food Upon the Pharmacokinetics of Androxal
NCT02146391 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Assess the Effects of Naproxcinod and Naproxen on Blood Pressure Measurements in Osteoarthritis Patients With Controlled High Blood Pressure
NCT00662610 ·Status: COMPLETED ·Phase: PHASE1