Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SR-TAC (Sustained-Release Tacrolimus) is a long-acting, subcutaneous injectable formulation of the immunosuppressant tacrolimus, developed by Auritec Pharmaceuticals. It utilizes Auritec's proprietary Plexis technology, which coats the active ingredient, tacrolimus monohydrate, with a biocompatible polymer to achieve sustained drug release over a 30-day period. Primarily indicated for the prophylaxis of organ transplant rejection, SR-TAC is designed to address common issues with daily oral tacrolimus therapies, such as poor medication adherence, high intra-patient variability, and dose-related toxicity. As a calcineurin inhibitor, tacrolimus prevents the activation of T-lymphocytes by inhibiting the phosphatase activity of calcineurin. The formulation has undergone Phase 1 clinical testing to assess its safety and pharmacokinetic profile in healthy volunteers.
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 SR-TAC.