Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Prednisolone + neomycin + polymyxin B** is an ophthalmic combination formulation containing the synthetic corticosteroid **prednisolone acetate** (5 mg/ml), aminoglycoside antibiotic **neomycin sulfate** (equivalent to 3.5 mg neomycin base), and polypeptide antibiotic **polymyxin B sulfate** (10,000 units/ml). Prednisolone reduces inflammation by binding glucocorticoid receptors to inhibit inflammatory mediators, while neomycin and polymyxin B disrupt bacterial cell walls and membranes to target gram-negative and gram-positive bacteria sensitive to these agents. It is primarily indicated for ocular disorders requiring concurrent anti-inflammatory and antibacterial therapy, such as nonpurulent conjunctivitis, blepharitis, scleritis, nonherpetic keratitis, dacryocystitis, and prophylaxis post-ocular surgery or trauma.[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 prednisolone + neomycin + polymyxin B.