Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Triamcinolone acetonide + anti-VEGF agent is a combination therapy, typically administered intravitreally, for retinal diseases characterized by macular edema, neovascularization, or inflammation (such as diabetic macular edema, radiation maculopathy, and branch retinal vein occlusion). Triamcinolone acetonide is a synthetic corticosteroid with potent anti-inflammatory and angiostatic activity, working by upregulating extracellular matrix proteins (like plasminogen activator inhibitor) and suppressing inflammatory cytokines and VEGF synthesis. Anti-VEGF agents (such as bevacizumab, ranibizumab, aflibercept, conbercept) inhibit vascular endothelial growth factor (VEGF), reducing abnormal blood vessel growth and vascular permeability. Together, these drugs act synergistically to lower inflammation, stabilize macular edema, and suppress angiogenesis, often reducing the need for repeated anti-VEGF injections, while preserving or improving visual acuity in some patient populations[1][3][4].
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 triamcinolone acetonide + anti-VEGF agent.