==== Reference: Usmani SS, Bedi G, Samuel JS, Singh S, Kalra S, Kumar P, et al. (2017) THPdb: Database of FDA-approved peptide and protein therapeutics. PLoS ONE 12(7) e0181748.====

Detailed description page of THPdb

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1529 details
Primary information
ThPP IDTh1108
Therapeutic Peptide/Protein NamePegaptanib
SequenceN.A. view full sequnce in fasta
Functional ClassificationIIa
Molecular WeightN.A.
Chemical FormulaN.A.
Isoelectric PointN.A.
HydrophobicityN.A.
Melting Point (℃)N.A.
Half Life10 ± 4 days
DescriptionIt is a polynucleotide aptamer, which specifically binds to VEGF 165, a protein that plays a critical role in angiogenesis and increased permeability of blood vessels; two of the primary pathological processes responsible for vision loss associated with neovascular AMD. [Wikipedia]
Indication/DiseaseFor the treatment of neovascular (wet) age-related macular degeneration.
PharmacodynamicsPegaptanib is a selective vascular endothelial growth factor (VEGF) antagonist. VEGF is a secreted protein that selectively binds and activates its receptors located primarily on the surface of vascular endothelial cells. VEGF induces angiogenesis, and increases vascular permeability and inflammation, all of which are thought to contribute to the progression of the neovascular (wet) form of age-related macular degeneration (AMD), a leading cause of blindness. VEGF has been implicated in blood retinal barrier breakdown and pathological ocular neovascularization.
Mechanism of ActionPegaptanib binds to the major pathological VEGF isoform, extracellular VEGF165, thereby inhibiting VEGF165 binding to its VEGF receptors. The inhibition of VEGF164, the rodent counterpart of human VEGF165, was effective at suppressing pathological neovascularization.
ToxicityMost common adverse reactions associated with the use of lucinactant are endotracheal tube reflux, pallor, endotracheal tube obstruction, and need for dose interruption.
MetabolismBased on preclinical data, pegaptanib is metabolized by endo- and exonucleases.
AbsorptionIn animals, pegaptanib is slowly absorbed into the systemic circulation from the eye after intravitreous administration.
Volume of DistributionN.A.
ClearanceN.A.
CategoriesIntended for the prevention of respiratory distress syndrome (RDS) in premature infants at high risk for RDS.
Patents NumberN.A.
Date of IssueN.A.
Date of ExpiryPulmonary
Drug InteractionN.A.
TargetN.A.
Information of corresponding available drug in the market
Brand NameMacugen
CompanyGilead Sciences
Brand DiscriptionPegaptanib sodium is a covalent conjugate of an oligonucleotide of twenty-eight nucleotides in length that terminates in a pentylamino linker, to which two 20-kilodalton monomethoxy polyethylene glycol (PEG) units are covalently attached via the two amino groups on a lysine residue.
Prescribed forMacugen is indicated for the treatment of neovascular (wet) age-related macular degeneration.
Chemical NameN.A.
FormulationMacugen is supplied in a single-dose, pre-filled syringe and is formulated as a 3.47 mg/mL solution, measured as the free acid form of the oligonucleotide. The active ingredient is 0.3 mg of the free acid form of the oligonucleotide without polyethylene glycol, in a nominal volume of 90 μL. This dose is equivalent to 1.6 mg of pegaptanib sodium (pegylated oligonucleotide) or 0.32 mg when expressed as the sodium salt form of the oligonucleotide moiety. The product is a sterile, clear, preservative-free solution containing sodium chloride, monobasic sodium phosphate monohydrate, dibasic sodium phosphate heptahydrate, hydrochloric acid, and/or sodium hydroxide to adjust the pH and water for injection.
Physcial AppearnceSterile, aqueous solution containing pegaptanib sodium for intravitreous injection
Route of AdministrationIntravitreal Injection ONLY
Recommended DosageMacugen 0.3 mg should be administered once every six weeks into the eye to be treated.
ContraindicationOcular or Periocular Infections: Macugen is contraindicated in patients with ocular or periocular infections.Hypersensitivity to pegaptanib sodium or any other excipient in this product.
Side EffectsThe most frequently reported adverse events in patients treated with Macugen 0.3 mg for up to two years were anterior chamber inflammation, blurred vision, cataract, conjunctival hemorrhage, corneal edema, eye discharge, eye irritation, eye pain, hypertension, increased intraocular pressure (IOP), ocular discomfort, punctate keratitis, reduced visual acuity, visual disturbance, vitreous floaters, and vitreous opacities; Ocular: blepharitis, conjunctivitis, photopsia, vitreous disorder.; Non-Ocular: bronchitis, diarrhea, dizziness, headache, nausea, urinary tract infection.
Useful Linkhttp://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=43224 http://www.bausch.com/ecp/our-products/rx-pharmaceuticals/rx-pharmaceuticals/macugen-pegaptanib-sodium-injection#.VP2PHculi1E http://www.rxlist.com/macugen-drug.htm
PubMed ID17717967, 17693999, 17687925, 23560774
3-D StructureN.A.