Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination is a multi-modal pain regimen (MMPR) consisting of acetaminophen, naproxen, gabapentin, oxycodone, and tramadol. It is utilized as the standard of care for managing acute pain in trauma patients, specifically within clinical research conducted by The University of Texas Health Science Center, Houston. The regimen employs a multi-mechanistic approach to analgesia: acetaminophen and naproxen inhibit prostaglandin synthesis via cyclooxygenase (COX) enzymes; gabapentin modulates voltage-gated calcium channels to reduce excitatory neurotransmitter release; and oxycodone and tramadol provide potent analgesia through mu-opioid receptor agonism. Tramadol additionally contributes to pain relief by inhibiting the reuptake of serotonin and norepinephrine. This specific combination was used as the control arm in the DOPE trial (NCT03928015) to evaluate the efficacy of adjunct dronabinol in reducing opioid consumption.
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 acetaminophen + naproxen + gabapentin + oxycodone + tramadol.