Specialty Pharmacy

NEW YORK and PRINCETON, N.J. — A drug designed to prevent stroke and systemic embolism in patients with atrial fibrillation has been accepted for review by the Food and Drug Administration.

Bristol-Myers Squibb and Pfizer said their investigational compound Eliquis (apixaban) was accepted for review and granted a priority-review designation. The companies submitted the application to the agency after completing two phase-3 trials, which examined the efficacy and safety of Eliquis among about 24,000 patients.

RALEIGH, N.C. — MedPro Rx president Nancy McFarlane won a Stevie Award for Best Entrepreneur, the specialty pharmacy provider said.

McFarlane won the award for the category of service businesses with up to 100 employers in the Stevie Awards for Women in Business, having led the company to multimillion-dollar sales over the past nine years, the company said. McFarlane founded the company in 2002.

LEXINGTON, Mass. — British drug maker Shire is looking to make a biotech drug for a rare genetic disorder at a new manufacturing plant in Massachusetts.

The company said Tuesday that it had filed with the Food and Drug Administration and the European Medicines Agency for approval to produce the Gaucher disease drug Vpriv (velaglucerase alfa) at its Lexington, Mass., plant. The company expects to win approval to make the drug there early next year.

ALTAMONTE SPRINGS, Fla. — BioPlus Specialty Pharmacy has appointed a new SVP to support the company's growth, the specialty pharmacy provider said.

The company announced the appointment of Elvin Montanez, PharmD, as SVP, saying he would contribute to BioPlus's development and implementation of growth strategies, noting that he had worked in leadership positions in health care for 20 years.

ALTAMONTE SPRINGS, Fla. — BioPlus Specialty Pharmacy announced that it now is allowing physicians to electronically submit prescriptions to its pharmacies.

BioPlus said its e-prescribing offering is designed to lessen the risk of errors, lower costs and improve compliance. The use of computerized medication order entry potentially could prevent up to 84% of dose, frequency and route errors in medication use, according to data from the Agency for Healthcare Research and Quality,a Department of Health and Human Services agency.

NEW YORK — Pfizer will acquire a San Diego-based drug maker focused on treatments for skin scarring, the company said Tuesday.

Pfizer said it would buy privately owned Excaliard Pharmaceuticals, whose lead product, EXC 001, is in phase-2 trials for skin scarring, also known as skin fibrosis, a result of surgical procedures. There currently are no Food and Drug Administration-approved treatments to reduce scar severity. Financial terms of the deal were not disclosed.

SILVER SPRING, Md. — After being unanimously recommended for approval by a Food and Drug Administration panel, the FDA has approved an eye disorder treatment created by Regeneron Pharmaceuticals.

THOUSAND OAKS, Calif. — A drug made by Amgen delayed the spread of prostate cancer to the bones in men with the disease and prolonged the survival of men with the condition, according to results of a late-stage clinical trial.