Clinical data | |
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Trade names | Prevymis |
Other names | AIC246; MK-8228 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a618006 |
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Routes of administration | By mouth, intravenous |
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Pharmacokinetic data | |
Bioavailability | 37% (estimate) |
Protein binding | 98.2% |
Metabolism | glucuronidation (UGT1A1/1A3) to a minor extent |
Elimination half-life | 12 hours |
Excretion | 93.3% via feces, <2% via kidneys |
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ECHA InfoCard | 100.232.644 |
Chemical and physical data | |
Formula | C29H28F4N4O4 |
Molar mass | 572.561 g·mol−1 |
3D model (JSmol) | |
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Letermovir (INN; brand name Prevymis) is an antiviral drug for the treatment of cytomegalovirus (CMV) infections. It has been tested in CMV infected patients with allogeneic stem cell transplants and may also be useful for other patients with a compromised immune system such as those with organ transplants or HIV infections.[3] The drug was initially developed by the anti-infective division at Bayer, which became AiCuris Anti-infective Cures AG through a spin-out and progressed the development to end of Phase 2 before the project was sold to Merck & Co for Phase 3 development and approval.[4]
The drug was granted fast track status by the US Food and Drug Administration (FDA) and orphan drug status by the European Medicines Agency.[3] It is approved for prevention of CMV infection and disease in recipients of an allogeneic stem cell transplant.[5]
The FDA considers it to be a first-in-class medication.[6]