SATIS_1170x120_1-25-21

Merck

Merck appoints Caroline Litchfield CFO

Merck appoints Caroline Litchfield CFO

KENILWORTH, N.J. — Merck announced Wednesday that Caroline Litchfield has been appointed executive vice president and chief financial officer (CFO), effective April 1, 2021. Litchfield succeeds Robert Davis; as previously announced (link), Davis, Merck’s current CFO, will become president of Merck, effective April 1, 2021, and will become chief executive officer on July 1, 2021.

Mike Nally to leave Merck; Frank Clyburn to lead all Merck Human Health

Mike Nally to leave Merck; Frank Clyburn to lead all Merck Human Health

KENILWORTH, N.J. — Merck announced that Michael Nally, chief marketing officer, Human Health, will leave the company at the end of March, and Frank Clyburn, chief commercial officer, Human Health, will become president, Human Health and lead all Human Health commercial and marketing for the company. Nally is leaving Merck for a leadership opportunity with

Merck and Gilead working together on HIV treatments

Merck and Gilead working together on HIV treatments

KENILWORTH, N.J. – Gilead Sciences and Merck today announced that they have entered into an agreement to co-develop and co-commercialize long-acting treatments in HIV that combine Gilead’s investigational capsid inhibitor, lenacapavir, and Merck’s investigational nucleoside reverse transcriptase translocation inhibitor, islatravir, into a two-drug regimen with the potential to provide new, meaningful treatment options for people

Merck to produce Johnson & Johnson COVID-19 vaccine

Merck to produce Johnson & Johnson COVID-19 vaccine

WASHINGTON  — Merck will help produce rival Johnson & Johnson’s newly approved coronavirus vaccine in an effort to expand supply more quickly, the White House reported Tuesday. This announcement comes as the White House looks to ramp up the production of the single-dose vaccine. Officials have said J&J faced unexpected production issues with its vaccine

Kenneth Frazier to retire as Merck CEO; board elects Davis as successor

Kenneth Frazier to retire as Merck CEO; board elects Davis as successor

KENILWORTH, N.J. — Merck announced that Kenneth Frazier, chairman and chief executive officer, will retire as CEO, effective June 30, 2021. Frazier will continue to serve on Merck’s board of directors as executive chairman, for a transition period to be determined by the board. The Merck board of directors has unanimously elected Robert M. Davis,

Merck discontinues development of SARS-CoV-2/COVID-19 vaccine candidates

Merck discontinues development of SARS-CoV-2/COVID-19 vaccine candidates

KENILWORTH, N.J. — Merck is discontinuing development of its SARS-CoV-2/COVID-19 vaccine candidates, V590 and V591, and plans to focus its SARS-CoV-2/COVID-19 research strategy and production capabilities on advancing two therapeutic candidates, MK-4482 and MK-7110. This decision follows Merck’s review of findings from Phase 1 clinical studies for the vaccines. In these studies, both V590 and

Merck to acquire OncoImmune

Merck to acquire OncoImmune

KENILWORTH, N.J. — Merck and OncoImmune, a privately-held, clinical-stage biopharmaceutical company,  announced that the companies have entered into a definitive agreement pursuant to which Merck, through a subsidiary, will acquire all outstanding shares of OncoImmune for an upfront payment of $425 million in cash. In addition, OncoImmune shareholders will be eligible to receive sales-based payments

Merck to acquire VelosBio

Merck to acquire VelosBio

KENILWORTH, N.J. — Merck and VelosBio Inc. announced Thursday that the companies have entered into a definitive agreement pursuant to which Merck, through a subsidiary, will acquire all outstanding shares of VelosBio for $2.75 billion in cash, subject to certain customary adjustments. VelosBio is a privately held clinical-stage biopharmaceutical company committed to developing first-in-class cancer

FDA approves Merck’s Recarbrio

FDA approves Merck’s Recarbrio

KENILWORTH, N.J. — Merck announced Friday that the U.S. Food and Drug Administration (FDA) has approved a supplemental New Drug Application (sNDA) for Recarbrio (imipenem, cilastatin, and relebactam) for the treatment of patients 18 years of age and older with hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia (HABP/VABP), caused by the following susceptible Gram-negative microorganisms.

IAVI and Merck collaborate to develop vaccine against SARS-CoV-2

IAVI and Merck collaborate to develop vaccine against SARS-CoV-2

KENILWORTH, N.J. — Merck  and IAVI, a nonprofit scientific research organization dedicated to addressing urgent, unmet global health challenges, today announced a new collaboration to develop an investigational vaccine against SARS-CoV-2 to be used for the prevention of COVID-19. This vaccine candidate will use the recombinant vesicular stomatitis virus (rVSV) technology that is the basis

Merck to acquire Themis

Merck to acquire Themis

KENILWORTH, N.J.— Merck  announced that the companies have entered into a definitive agreement under which Merck, through a subsidiary, will acquire privately-held Themis. Themis has a broad pipeline of vaccine candidates and immune-modulatory therapies developed using its innovative measles virus vector platform based on a vector originally developed by scientists at the Institut Pasteur, a

Merck announces appointment of Organon & Co. CFO and CIO

Merck announces appointment of Organon & Co. CFO and CIO

KENILWORTH, N.J. — Merck, known as MSD outside the United States and Canada, announced the appointment of Matthew Walsh and Rachel Stahler as chief financial officer and chief information officer, respectively, for Organon & Co., its intended spinoff of its women’s health, legacy brands and biosimilars businesses. In his new role at Organon, Walsh will

Merck and ISB team to define molecular mechanisms of SARS-CoV-2 infection

Merck and ISB team to define molecular mechanisms of SARS-CoV-2 infection

KENILWORTH, N.J. — Merck and the Institute for Systems Biology (ISB), announced on Monday a new research collaboration to investigate and define the molecular mechanisms of SARS-CoV-2 infection and COVID-19 and identify targets for medicines and vaccines. Merck has also entered into an agreement with the Biomedical Advanced Research and Development Authority (BARDA), part of

Merck announces launch of Ontruzant

Merck announces launch of Ontruzant

KENILWORTH, N.J. — Merck announced the U.S. launch of Ontruzant (trastuzumab-dttb), as a biosimilar of the reference biologic medicine Herceptin. Ontruzant is available in both 150 mg single-dose vials and 420 mg multiple-dose vials. Ontruzant will be introduced in the U.S. at a list price (wholesaler acquisition cost) of approximately $1,325 for the 150 mg