TKL Research, Inc.
Fair Lawn, New Jersey, 07410, United States
NCT Number: NCT06415019
Researchers are looking for a better way to treat muscle and joint pain. Researchers have seen that medicines which help reduce pain and inflammation could be safer when applied directly to the skin, called topical application, than when taken by mouth. However, recent studies have found that using these medicines on the skin can sometimes cause skin reactions such as redness, itching, or irritation in the area where the medicine is applied. However, reports of more serious side effects, affecting the entire body, from using these topical medicines are uncommon.
The study treatment BAYH006689 is under development to treat muscle and joint pain.
In this study, participants will be healthy and will not benefit from BAYH006689. However, the study will provide information on how to test BAYH006689 in future studies in people with muscle and joint pain.
The main purpose of this study is to check if BAYH006689 topical gel causes any skin reactions in healthy participants. The skin reactions will be assessed using a scale. This scale will provide scores for redness, swelling, and other signs of skin irritation.
In this study, researchers will randomly assign 3 sites, adjacent to each other, on the back of participants' bodies just below the shoulder blades.
The following gels will be applied 10 times at these sites as a patch three times a week for 21 days and once after 14-17 days:
* BAYH006689 * Placebo, which looks like the study drug but does not have any medicine in it. * 0.9 % saline
Each participant will be in the study for around 6 to 8 weeks. During this time they will:
* receive assigned treatment gels at the identified skin sites * have their skin reaction symptoms assessed
During the study, the doctors and their study team will:
* check the medical history of the participants * check participants' health by performing urine tests * ask the participants questions about how they are feeling and what adverse events they are having An adverse event is any medical problem that a participant has during a study. Doctors keep track of all adverse events, irrespective of whether they think they are related or not to the study treatment.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 1
Fair Lawn, New Jersey, 07410, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
BAYH006689 gel will be dispensed directly on the patch
Placebo gel will be dispensed directly on the patch
0.9% Saline will be dispensed directly on the patch.
Time frame: Up to 12 weeks
Skin sensitization will be based on specific scoring criteria.
Bayer
Industry
A Randomized, Controlled Study to Evaluate the Sensitizing Potential of BAY H006689, Naproxen 10% Topical Gel in Healthy Subjects Using a Repeat Insult Patch Test Design
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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