Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Reproxalap is a first-in-class small molecule drug candidate developed for the treatment of dry eye disease and allergic conjunctivitis. It acts as a modulator and inhibitor of reactive aldehyde species (RASP), which are elevated in ocular and systemic inflammatory diseases. By inhibiting RASP, reproxalap reduces ocular inflammation, diminishes tear production issues, redness, and changes in tear lipid composition associated with dry eye disease. The drug has also been investigated for noninfectious anterior uveitis and Sjögren-Larsson syndrome, where it holds orphan drug status. Reproxalap works by rapidly binding to RASP such as malondialdehyde (MDA) and 4-hydroxy-2-nonenal (HNE), thereby preventing their pro-inflammatory effects mediated through pathways like NF-kB translocation, inflammasome activation, and scavenger receptor A binding[1][2][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 reproxalap.