US regulators OK updated version of decades-old antibiotic

TRENTON, N.J.: U.S. regulators on Tuesday approved a modernized version of a decades-old antibiotic used to treat a number of infections.

Paratek Pharmaceuticals’ Nuzyra was designed to overcome the problem of resistance to tetracycline, an antibiotic widely used until recent years.

The company said the Food and Drug Administration approved Nuzyra for treating bacterial pneumonia and severe skin infections.

Paratek plans to launch the antibiotic early next year, initially for use in hospitals. It hasn’t disclosed the price.

Boston-based Paratek estimates its drug could eventually treat nearly 900,000 hospitalized U.S. patients annually

About 2 million Americans get infections from antibiotic-resistant bacteria each year and 23,000 die, according to the Centers for Disease Control and Prevention.

Paratek tested Nuzyra against several types of bacteria that cause pneumonia and skin infections. The drug was more effective than two standard antibiotics given to patients in comparison groups, company testing showed.

Many antibiotics no longer work well, if at all, against some bacterial infections, due to their overuse in medicine and livestock production.

Paratek’s drug, also known as omadacycline, is the first in a new class of antibiotics. It’s an updated version of tetracycline, a 65-year-old antibiotic that was a workhorse against skin, respiratory and other infections until increasing resistance limited its use. Paratek created its drug by tweaking tetracycline to block two common ways bacteria use to resist it.

The FDA approved both an IV version and a daily pill that patients can switch to when they leave the hospital, the company said. It will eventually market the drug for patients treated at doctors’ offices and clinics.

Last week, the U.S. Health and Human Services Department announced at the United Nations General Assembly a new global effort to fight antibiotic resistance and develop new treatments. The 106 initial participants included drugmakers, government agencies, medical groups and animal food producers.

  • Related Posts

    Telangana HM orders action against misleading pharma ads, sale of substandard drugs

    Hyderabad: In a stern message to the pharmaceutical industry, Telangana Health Minister Damodar Rajanarsimha has ordered the Drug Control Authority (DCA) to take stringent action against companies and individuals involved…

    LOC issued against man who sold fake Ozempic worth Rs 180 crore to US firm

    New Delhi:  A lookout circular (LOC) has been issued against the man who allegedly sold fake Ozempic worth Rs 180 crore to a United States-based firm, officers have said. According…

    Leave a Reply

    Your email address will not be published. Required fields are marked *

    You Missed

    Telangana HM orders action against misleading pharma ads, sale of substandard drugs

    Telangana HM orders action against misleading pharma ads, sale of substandard drugs

    Aurobindo Pharma clarifies, reports of Zentiva buyout ‘premature’, no binding agreement yet

    Aurobindo Pharma clarifies, reports of Zentiva buyout ‘premature’, no binding agreement yet

    AIIMS study finds catheter infections in hospital widespread across India

    AIIMS study finds catheter infections in hospital widespread across India

    MNCs seek restart of refurbished medical device imports

    MNCs seek restart of refurbished medical device imports