Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Vycavert** was an investigational immediate-release fixed-dose oral analgesic tablet containing hydrocodone bitartrate and acetaminophen, developed by Acura Pharmaceuticals using its AVERSION abuse-deterrent technology. Hydrocodone provides opioid analgesia through mu-opioid receptor agonism, while acetaminophen provides non-opioid analgesic activity. The AVERSION formulation incorporated tamper-deterrent features intended to discourage intranasal and intravenous misuse of crushed tablets. Clinical studies evaluated oral bioequivalence against Norco and the abuse potential of intranasally administered crushed Vycavert in non-dependent recreational opioid users. Acura's later LIMITx candidate LTX-03 is a distinct hydrocodone/acetaminophen formulation and should not be treated as the same product. ([clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01456520))
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Vycavert.