Merck announced that its Life Science business sector has doubled its high-potent active pharmaceutical ingredients (HPAPI) production capacity with the expansion of its facility in Verona, near Madison, Wisconsin, US. This new €59 million, 70,000 square foot facility, officially opened, brings 50 new jobs to the area.

"There is an increasing demand for HPAPIs due to their effectiveness against cancer at lower doses and the trend towards more targeted therapeutics. Lower doses of these therapies reduce the negative side effects for patients who are taking on this critical fight," said Dirk Lange, head of Life Science Services, Life Science, at Merck. "Increasing capacity at our state-of-the-art CDMO facility in Verona, Wisconsin will allow us to meet the need for these key cancer treatment components."

Merck's Verona, Wisconsin site was the second facility in the world to be SafeBridge-certified and the company continues to meet these rigorous safety and containment requirements necessary to this day. In fact, this expansion positions Merck as one of the largest single-digit nanogram occupational exposure limit (OEL) CDMO providers in the world. HPAPIs are measured with the most potent registering less than 10 nanograms per cubic meter. Single-digit nanogram HPAPIs require highly specialised handling, which is reflected by the OEL designation.

In addition to HPAPI production, Merck also has extensive experience developing and manufacturing ADCs. Being the first CDMO to manufacture commercially approved ADC drugs in North America, the company recently launched new technologies to advance ADC therapies. Its unique ChetoSensar technology gives new promise to ADCs by alleviating solubility challenges, and Merck's new DOLCORE platform significantly reduces the development and manufacturing time required, increasing speed-to-market by up to a year, ultimately getting needed therapies to patients quicker.

With more than 30 years of CDMO experience in the development and manufacturing of HPAPIs, linkers and mAbs, Merck offers significant expertise in both clinical and commercial manufacturing. The company also has extensive CDMO experience in viral vector, lipids, LNP and mRNA manufacturing— from pre-clinical to commercial — helping to streamline steps of drug development and production with a single, highly experienced partner. Additionally, BioReliance contract testing services are integrated into the overall services offering to further streamline the development path.