Nabriva Therapeutics recruit new COO

pharmafile | July 12, 2017 | Appointment | Business Services, Manufacturing and Production, Medical Communications, Research and Development, Sales and Marketing Nabriva Therapeutics, biotech, drugs, pharma, pharmaceutical 

Nabriva Therapeutics, a pharmaceutical company that is developing new antibiotics for the treatment of serious infections, has brought Francesco Maria Lavino to the company from MSD to perform the role of Chief Commercial Officer.

Lavino joins the company having managed MSD’s anti-bacterial portfolio, in varying positions sales and marketing positions. In total, he spent over 12 years at MSD, where he progressed from Marketing Manager for the Cardiovascular Market to Associate Vice President and Global Brand Leader Antibiotics Portfolio. He also had close to two years’ experience as Cubist Pharmaceuticals’ Vice President of International Marketing.

Lavino commented on his appointment to the new role: “There has been a dearth of innovation in the development of new anti-infective medicines…Nabriva Therapeutics is poised to introduce what is potentially the first new class of antibiotics for systemic human use in nearly two decades. I am looking forward to working with Will, Colin and the rest of the management team to address serious medical needs in lung, skin, and potentially other types of infections.”

Lavino refers to the Phase 3 global clinical trials for lefamulin, a semi-synthetic antibiotic for community-acquired bacterial pneumonia. Should the antibiotic succeed in these trials, Lavino would be responsible for the marketing of the drug to doctors on a regional and national basis.

“Nabriva Therapeutics is on the cusp of a major inflection point, as we work toward the potential approval of the first pleuromutilin antibiotic for the treatment of community-acquired bacterial pneumonia,” said Colin Broom, CEO. “Francesco has the right experience and leadership qualities to build out a fully integrated commercial team and hospital field force in the United States, and I am delighted to welcome him as part of our team.” 

Related Content

FDA approves IMIDEX’s AI-powered device VisiRad XR

The technological pharmaceutical company IMIDEX has been granted clearance from the US Food and Drug …

Artiva Biotherapeutics announces FDA clearance of IND for AlloNK and Rituximab combo

On 16 August 2023, the US Food and Drug Administration (FDA) officially cleared Artiva Biotherapeutics’ …

Zumutor’s cancer drug trial cleared by FDA

On 11 August 2023, the biopharmaceutical company Zumutor Biologics announced that the trial of its …

Latest content