Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
STAR-LLD-OCR is an oral controlled-release formulation of lenalidomide being developed by Starton Therapeutics. It utilizes a continuous low-dose delivery platform (STAR-LLD) designed to maintain therapeutic levels of lenalidomide while potentially reducing the hematologic toxicities associated with standard pulsatile oral dosing (e.g., Revlimid). Lenalidomide is an immunomodulatory drug (IMiD) that acts by binding to cereblon (CRBN), a component of the CRL4-CRBN E3 ubiquitin ligase complex. This binding triggers the selective ubiquitination and subsequent proteasomal degradation of lymphoid transcription factors IKZF1 (Ikaros) and IKZF3 (Aiolos), leading to anti-neoplastic and immunomodulatory effects. The OCR formulation is specifically being investigated for high-risk relapsed/refractory multiple myeloma and chronic lymphocytic leukemia.
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 STAR-LLD-OCR.