Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lademirsen is an investigational antisense oligonucleotide therapy developed for the treatment of Alport syndrome, a hereditary kidney disease. It functions as an anti–microRNA-21 (miR-21) agent, inhibiting miR-21 to reduce renal fibrosis and slow the progression of kidney dysfunction. Lademirsen was administered via subcutaneous injection and underwent clinical evaluation in Phase 2 trials for Alport syndrome. The drug was originally developed by Regulus Therapeutics in collaboration with Sanofi, but development was discontinued after Phase 2 trials[3][4][5][6][8].
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 lademirsen.