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Astellas Pharma Europe Ltd., has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of marketing authorisation for VIBATIV (telavancin hydrochloride) for the treatment for adults with nosocomial (hospital-acquired) pneumonia, including ventilator associated pneumonia known or suspected to be caused by MRSA (methicillin resistant Staphylococcus aureus). VIBATIV should be used only in situations where it is known or suspected that other alternatives are not suitable. VIBATIV is a bactericidal, once-daily injectable lipoglycopeptide antibiotic developed by Theravance, Inc..
The CHMP, on the basis of quality, safety and efficacy data submitted, considered there to be a favourable benefit to risk balance for VIBATIV and therefore recommended the granting of the marketing authorisation.
The CHMP’s positive opinion is a critical step in the approval process, and it is expected that the European Commission will follow the advice of the CHMP and grant marketing authorisation in approximately two to three months. If approved, it would allow Astellas to make the product available to healthcare professionals trying to meet the challenge of treating serious hospital-acquired lung infections caused by MRSA.
“This positive opinion from the CHMP for VIBATIV is great news for both doctors and patients who continue to battle serious life-threatening nosocomial pneumonia, including ventilator associated pneumonia caused by MRSA,” said Ken Jones, President and CEO, APEL. “It means healthcare professionals will soon have a new, effective hospital antibiotic with potent bactericidal activity against Gram-positive bacteria and potentially a higher likelihood of generating successful clinical outcomes in certain critically ill patients who increasingly fail to respond to established therapy,” he added.
The European Centre for Disease Prevention and Control (ECDC) estimate that each year more than 4 million patients in Europe acquire an infection in hospital. At least 37,000 Europeans die as a direct result of hospital-acquired infections. Risk factors for contracting a hospital-acquired infection due to MRSA include older age, prolonged hospitalisation, intravenous drug use and diabetes. MRSA is the most frequent cause of ventilator-associated pneumonia and the second highest cause of mortality in these critically ill patients.
Across Europe there is a high unmet need for new drugs which are active against MRSA and other Gram-positive pathogens particularly with poor susceptibility to more commonly used antibacterials.
VIBATIV, licensed from Theravance, Inc. for global commercialisation, is a bactericidal, once-daily, injectable lipoglycopeptide antibiotic with a dual mechanism of action against Gram-positive bacteria including resistant pathogens such as MRSA. In Phase 3 clinical trials, more than 750 patients with nosocomial pneumonia, including a subset of patients with ventilator associated pneumonia, have been treated with VIBATIV.
In phase 3 clinical trials ATTAIN I and ATTAIN II VIBATIV has demonstrated non-inferiority to vancomycin in the primary endpoint of clinical cure, with better outcomes in certain patient populations.
VIBATIV was approved in the United States in September 2009, and in Canada in October, 2009 for adult patients with complicated skin and skin structure infections (cSSSI) caused by susceptible Gram-positive bacteria.
Astellas has an ongoing commitment to combating infectious diseases through the worldwide launch of its injectable antifungal echinocandin, MYCAMINE® (micafungin), which has been used to treat over 750,000 patients worldwide. In addition, Astellas has entered into a global partnership with Basilea Pharmaceuticals Ltd. to co-develop and co-promote isavuconazole, an azole antifungal for the treatment of invasive fungal infections, including Aspergillosis, currently in Phase 3 trials; and with Optimer Pharmaceuticals Inc. to develop and commercialise fidaxomicin, an investigational antibiotic under regulatory review as a novel treatment for Clostridium difficile infection in Europe and certain other countries.
