Ocriplasmin
Recombinant protease with activity against fibronectin and laminin
title: "Ocriplasmin" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["enzymes-used-as-drugs", "ophthalmology-drugs"] description: "Recombinant protease with activity against fibronectin and laminin" topic_path: "general/enzymes-used-as-drugs" source: "https://en.wikipedia.org/wiki/Ocriplasmin" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0
::summary Recombinant protease with activity against fibronectin and laminin ::
::data[format=table title="Infobox drug"]
| Field | Value |
|---|---|
| tradename | Jetrea |
| Drugs.com | |
| licence_EU | yes |
| pregnancy_AU | B2 |
| routes_of_administration | Intravitreal |
| ATC_prefix | S01 |
| ATC_suffix | XA22 |
| legal_AU | S4 |
| legal_AU_comment | |
| legal_CA | |
| legal_UK | |
| legal_US | Rx-only |
| legal_EU | Rx-only |
| CAS_number | 1048016-09-6 |
| IUPHAR_ligand | 7446 |
| DrugBank | DB08888 |
| UNII_Ref | |
| UNII | 7V6HE3DM5A |
| ChemSpiderID | none |
| KEGG | D09646 |
| C | 1214 |
| :: |
| IUPAC_name = | image = | alt = | caption =
| tradename = Jetrea | Drugs.com = | MedlinePlus = | licence_EU = yes | pregnancy_AU = B2 | pregnancy_category= | routes_of_administration = Intravitreal | ATCvet = | ATC_prefix = S01 | ATC_suffix = XA22
| legal_AU = S4 | legal_AU_comment = | legal_CA = | legal_UK = | legal_US = Rx-only | legal_EU = Rx-only | legal_status =
| bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion =
| CAS_number = 1048016-09-6 | PubChem = | IUPHAR_ligand = 7446 | DrugBank = DB08888 | UNII_Ref = | UNII = 7V6HE3DM5A | ChemSpiderID = none | KEGG = D09646
| C=1214 | H=1890 | N=338 | O=348 | S=14
Ocriplasmin, sold under the brand name Jetrea, is a recombinant protease with activity against fibronectin and laminin, components of the vitreoretinal interface. It is used for treatment of symptomatic vitreomacular adhesion, for which it received FDA approval on 17 October 2012. It works by dissolving the proteins that link the vitreous to the macula, resulting in posterior detachment of the vitreous from the retina.
Structure
Ocriplasmin is an injectable drug that is "a truncated form of the human serine protease plasmin." The protease plasmin still retains its enzymatic properties. Ocriplasmin consists of two polypeptide chains that are linked by disulfide bonds. Additionally, the longer peptide chain has four disulfide bonds. Ocriplasmin is only moderately stable when injected, and this is due to autolytic degradation.
Mechanism of action
Ocriplasmin can degrade various structural proteins, including laminin and fibronectin, which are localized in the vitreoretinal surface. Here, these two proteins are involved in vitreoretinal attachment. Ocriplasmin is currently being studied in clinical trials and data indicate that it is able to induce posterior vitreous detachment in vitreomacular adhesion patients.
FDA regulation
ThromboGenics, the manufacturer of ocriplasmin, encountered several problems when trying to get approval for the drug. In 2012, the FDA brought up the problem of adverse side effects associated with the drug. The FDA stated that the adverse effects may not cause long-term harm, but that conclusion could not be definitively made. Several days later, the FDA endorsed ocriplasmin, which was still an experimental drug. The advisory committee brought up several safety issues, but the committee ended up voting that no additional studies were needed. This may be controversial, considering the drug underwent only two studies.
Sales
As part of a deal with Alcon, ThromboGenics received $98.4 million for the ex-US rights to ocriplasmin. This is part of a $500 million-plus deal. ThromboGenics received a $123 million-plus payment, when ocriplasmin gained approved in the European Union; this occurred in March 2013.
60% of the market of ocriplasmin is in the United States, with more than a quarter of a million patients.
References
References
- (21 June 2022). "Prescription medicines: registration of new chemical entities in Australia, 2014".
- (August 2012). "Enzymatic vitreolysis with ocriplasmin for vitreomacular traction and macular holes". The New England Journal of Medicine.
- [http://www.european-biotechnology-news.com/news/news/2012-03/fda-panel-backs-ocriplasmin.html "FDA panel backs ocriplasmin."] {{Webarchive. link. (2016-03-04 (2012) ''European Biotechnology News.'')
- (May 2012). "Mechanism of inactivation of ocriplasmin in porcine vitreous". Biophysical Chemistry.
- (2012). "ThromboGenics jolted with safety questions on eve of FDA panel review.". FierceBiotech.
- (2012). "ThromboGenics wins FDA panel nod for eye drug.". FierceBiotech.
- (2012). "FDA approvals: ocriplasmin for vitreomacular adhesions.". MedScape.
- (2013). "ThromboGenics Signs Potential $494M Ex-U.S. Ocriplasmin Deal". BioWorld.
- (15 March 2013). "ThromboGenics' JETREA granted EU approval for vitreomacular traction (VMT), including when associated with macular hole of diameter less than or equal to 400 microns".
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