Provepharm receives favorable EMA Review of its methylthioninium chloride Proveblue
The French Health Safety Agency Afssaps already granted a Compassionate Use Authorization (”ATU de cohorte” in French) for methylthioninium chloride Proveblue on 22 November 2010, which enabled Provepharm to make the product available to French hospitals.
Methylthioninium chloride (or methylene blue) has always been used extensively in diagnostic and therapeutic applications. Up to now, however, it generally contained high levels of heavy metals that were toxic for patients. Provepharm has developed a new process that has considerably reduced the amounts of organic and inorganic impurities (heavy metals) in the compound. This process was considered innovative by the European authorities, enabling Provepharm to submit an MAA under the EMA’s centralized review procedure. The patents filed by Provence Technologies, Provepharm’s parent company which developed Proveblue(TM), protect this innovation up to 2027.
“This first marketing authorization gives Provepharm very substantial commercial potential, with annual revenues forecast to reach EUR 30 to 40 million within five years,” said Provepharm’s chairman, Michel Féraud. “We are actively looking for distributors in the different markets covered by the MAA, and we also hope to make the product available in other markets, starting with the United States and Japan. Talks are underway to select partners in these two regions.”
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