XenoPort Announces Presentation Of XP13512 Data At The American Pain Society Meeting

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Pharmacokinetic analysis show signs of that, not considering self administered at a subjugate molar daily dose (2400 mg XP13512 can maximally unchain 1248 mg gabapentin), XP13512 produced a mean percentage increase of 17% in the average plasma focus of gabapentin equate to that produced by Neurontin in like lenient (p=0.005). Analysis of all patients in the XP13512 treatment arm indicate that MPS be lower at the end of XP13512 treatment compared to the end of Neurontin treatment (difference=-0.4; p=0.0454). A subgroup of patients (36% of total) enjoy an increased average plasma concentration of gabapentin of greater than 30% during XP13512 treatment compared to Neurontin treatment. The overhaul in MPS from the end of Neurontin treatment to the end of XP13512 treatment was more pronounced here jumble (difference=-0.9; p=0.0126) and was not see in a subgroup of patients whose average gabapentin concentration was smaller amount than 20% resounding while on XP13512 compared to Neurontin (difference=-0.2; p=0.4841). XP13512 was okay tolerate in this study.

About XP13512 XP13512 be a Transported Prodrug of gabapentin, a linctus that have be sold by Pfizer Inc as Neurontin since 1993 and is at the moment sold as a generic drug by a figure of company. XP13512 utilize high-capacity carrying heart-rending parts to be well affianced in the trifling and massive innards and is designed to after at a fast pace convert to gabapentin upon incorporation from the gastrointestinal tract. Besides gabapentin, the metabolic breakup products of XP13512 be molecules that have undergone general safekeeping trialling and are found by instinct in mammals and in diet. Phase 1 clinical trial in powerful volunteers have demonstrated that, in judgment to Neurontin, oral authority of XP13512 construct dose-proportional blood level of gabapentin across a extensive band of dose. XP13512 has victoriously completed a Phase 2 clinical program for the treatment of Restless Legs Syndrome, or RLS, and has commence a Phase 3 clinical program in RLS patients. XP13512 has been well tolerated in all clinical trials completed to date.