The goal of this clinical trial is to test the ability of HT-6184 to decrease inflammation and pain in patients after third molar removal. The main question it aims to answer are: * Does HT-6184 decrease inflammation in patients after third molar removal? * Does HT-6184 decrease pain in patients after third molar removal? Participants will be asked to do the following during the clinical trial: * Take a single oral dose of HT-6184 or placebo * Allow a oral surgeon remove their third molar teeth * Blood draws on 5 occurrences * Rate their pain intensity * Attend two follow-up appointments on day 1 and day 2 after third molar removal * Participate in one follow-up phone call 5-7 days after third molar removal
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
81
Single, oral dose of HT-6184
Single, oral dose of placebo
CenExel JBR
Murray, Utah, United States
Change in serum C-reactive protein levels from pre-dose
Time frame: Up to 54 hours post surgery
Incidence of adverse events
Severity of AEs will be judged according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Time frame: Up to 7 days post surgery
Incidence of serious adverse events
Severity of AEs will be judged according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Time frame: Up to 7 days post surgery
Area under the categorical pain intensity-by-time curve (AUCs)
Time frame: Up to 8 hours after surgery
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