This is a study to understand if taking VTX2735 is safe and effective in participants diagnosed with Recurrent Pericarditis (RP). Cohort A will include up to 30 participants and will consist of the following: * A 30-day Screening Period (to see if a participant qualifies for the study) * A 6-week Open Label Treatment Period - participant receives VTX2735 Dose A * A 7-week Extension Treatment Period (if a participant meets criteria for extension treatment) - participant receives VTX2735 Dose A * An 11-week Once Daily Treatment Period (if a participant meets criteria for this treatment period) - participant receives VTX2735 Dose B * A 14-day Follow-Up Period Cohort B will include up to 20 participants and will consist of the following: * A 30-day Screening Period (to see if a participant qualifies for the study) * A 6-week Open Label Treatment Period - participant receives VTX2735 Dose B or C * An 18-week Extension Treatment Period (if a participant meets criteria for extension treatment) - participant receives VTX2735 Dose B or C * A 14-day Follow-Up Period
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Dose A, daily
Dose B, Daily
Dose C, daily
Local Site #840012
Tucson, Arizona, United States
RECRUITINGLocal Site #840014
Orange, California, United States
RECRUITINGLocal Site #840016
Saint Augustine, Florida, United States
RECRUITINGLocal Site #840008
Chicago, Illinois, United States
RECRUITINGLocal Site #840002
Park Ridge, Illinois, United States
RECRUITINGLocal Site #840011
Owensboro, Kentucky, United States
WITHDRAWNLocal Site #840010
Boston, Massachusetts, United States
RECRUITINGLocal Site #840005
Rochester, Minnesota, United States
RECRUITINGLocal Site #840020
New York, New York, United States
RECRUITINGLocal Site #840017
Cleveland, Ohio, United States
RECRUITING...and 6 more locations
Safety and tolerability of VTX2735
Incidence of adverse events (AEs), serious adverse events (SAEs), and AEs leading to study treatment discontinuation
Time frame: Day 1 of treatment period through study completion, up to 26 weeks
Effect of VTX2735 on pericardial pain
Change from baseline in Numeric Pain Rating Scale (NRS) over time through Week 6
Time frame: Day 1 of treatment period to Week 6 of treatment period
Effect of VTX2735 on inflammation
Change from baseline in High-Sensitivity C-Reactive Protein (hs-CRP) over time through Week 6
Time frame: Day 1 of treatment period to Week 6 of treatment period
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.