Chimerix Completes Phase I Study and Initiates a Phase II Multi-dose Clinical Trial for CMX001
Posted on: Tuesday, 6 January 2009, 07:00 CST
"The safety and high oral availability demonstrated by CMX001 in the Phase
I trial has exceeded our original expectations," said Dr.
The Phase I study of CMX001 was a blinded, randomized, placebo-controlled study that evaluated the safety and pharmacokinetics of orally administered CMX001 in healthy volunteers. The study found CMX001 to be well tolerated at all doses in 84 healthy volunteers.
The first Phase II trial will study the effects of multiple doses of CMX001 given to stem cell and kidney transplant recipients with BK viruria, a condition which may eventually lead to loss of the kidney graft, or to uncontrolled bleeding in the bladder. Further studies are planned to explore the ability of CMX001 to prevent cytomegalovirus disease, a viral disease that may lead to blindness or severe gastrointestinal disease after bone marrow transplant.
CMX001 is being developed for the treatment of smallpox infection and
other double stranded DNA virus infections that cause significant human
morbidity and mortality. A safe, orally active antiviral drug to treat
smallpox infection is needed to help people who become ill after exposure to
the disease or those who cannot be vaccinated. The work is partially funded
by a
About Chimerix
Chimerix, Inc. discovers, develops and commercializes therapeutics with enhanced pharmaceutical properties that are active against a broad range of viral diseases. Leveraging a powerful lipid, prodrug technology, ProLipTag(TM), Chimerix is able to develop drug candidates with oral-availability, increased potency and targeted delivery. These enhanced pharmaceutical properties can be applied to new drug moieties or known drugs to improve dosing parameters, broaden therapeutic applications and decrease the risk of adverse events.
SOURCE Chimerix, Inc.
Source: PR Newswire
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