Condition: Postsurgical Pain Management · Sponsor: TLC Biopharmaceuticals, Inc.
This Phase 2 open-label trial investigates the pharmacokinetics (PK), pharmacodynamics, and safety profile of TLC590 across various surgical procedures. Researchers aim to determine the maximum tolerated dose (MTD) of TLC590 via Safety Monitoring Committee (SMC). The study evaluates TLC590 in bunionectomy, laparoscopy-assisted open ventral hernia repair, breast augmentation, abdominoplasty, and total knee arthroplasty models. Additionally, it determines the relative bioavailability of TLC590 to ropivacaine injection.
This description comes directly from the study's public registry record.
Jack Chang · +886-2-26557377 · Jack@tlcbio.com
Always discuss trial participation with your own doctor first.
| First Surgical Hospital | Bellaire, Texas, United States | Recruiting |
| Memorial Hermann Village | Houston, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06574269