ContraVir Pharmaceuticals Announces Data on Optimized Formulation of TXL™
TXL™ has been designed to target the liver to deliver the active drug to the reservoir where the hepatitis B virus resides. TXL™ displayed a favorable safety and tolerability profile in a completed Phase 2a study of HBV patients at doses up to 100 mg. The Phase 2a study confirmed that TXL™ administration resulted in lower circulating levels of tenofovir (TFV), compared with levels observed after administration of Viread® (tenofovir disoproxil fumarate, TDF). Higher circulating levels of TFV, associated with TDF, have previously been shown to cause kidney and bone toxicities. Importantly, TXL™ dosing reduced viremia (HBV DNA) to the same extent as TDF, while minimizing TFV levels associated with these well-known toxicities.
ContraVir undertook studies to optimize the formulation of TXL™ to allow for more efficient, predictable, and precise delivery to the target organ (i.e., liver), thereby potentially reducing drug burden while maintaining consistent efficacy. The optimization of TXL™ was additionally designed to diminish the impact of physiological variables allowing for more consistent delivery of the prodrug to the site of action. Consistent and predictable target organ delivery is necessary, especially as curative combination regimens are developed for a functional cure.
“The ultimate goal in enhancing drug formulation is to offer a potential therapeutic benefit that could allow for more precise and predictive dosing while remaining safe and well tolerated,” said
The objective of the next clinical trial with TXL™ will be to characterize the pharmacokinetic profile of the new formulation in HBV patients, and to select the target dose to be advanced into a Phase 3 registration clinical development program.
ContraVir is a biopharmaceutical company focused on the development and commercialization of targeted antiviral therapies with a specific focus on developing a potentially curative therapy for hepatitis B virus (HBV). The company is developing two novel anti-HBV compounds with complementary mechanisms of action. TXL™, a nucleoside analog lipid prodrug of tenofovir (TFV), is designed to deliver higher hepatic intracellular concentrations of the active tenofovir species (tenofovir diphosphate) while reducing concentrations of tenofovir outside the liver, causing fewer off-target toxicities and side-effects. CRV431, the other anti-HBV compound, is a next-generation cyclophilin inhibitor with a novel structure that increases its potency and selective index against HBV. In vitro and in vivo studies have thus far demonstrated that CRV431 reduces HBV DNA and other viral proteins, including surface antigen (HBsAg). For more information visit www.contravir.com.
Forward Looking Statements
Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by the use of forward-looking words such as “anticipate,” “believe,” “forecast,” “estimated,” and “intend,” among others. These forward-looking statements are based on ContraVir’s current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. These factors include, but are not limited to, substantial competition; our ability to continue as a going concern; our need for additional financing; uncertainties of patent protection and litigation; uncertainties with respect to lengthy and expensive clinical trials, that results of earlier studies and trials may not be predictive of future trial results; uncertainties of government or third party payer reimbursement; limited sales and marketing efforts and dependence upon third parties; and risks related to failure to obtain
For further information, please contact:
Director of Investor Relations
firstname.lastname@example.org; (732) 902-4028
Source: ContraVir Pharmaceuticals Inc.