Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy refers to the pharmacological components of the Duke University 'PARTNER UP' program, a telemedicine-based harm reduction intervention designed for people who inject drugs (PWID). The program integrates the administration of two fixed-dose combination medications: buprenorphine/naloxone (Suboxone) for medication for opioid use disorder (MOUD) and tenofovir disoproxil fumarate/emtricitabine for HIV pre-exposure prophylaxis (PrEP). Buprenorphine acts as a partial mu-opioid agonist to reduce cravings and withdrawal symptoms, while naloxone is included as an abuse deterrent. The PrEP component consists of two nucleoside reverse transcriptase inhibitors (NRTIs) that prevent HIV replication. The program was piloted at syringe services programs in North Carolina to assess the feasibility of using telemedicine for follow-up care in this high-risk population.
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 buprenorphine + naloxone + tenofovir disoproxil fumarate + emtricitabine.