Eight out of 10 covered U.S. commercial lives now have access to the H. pylori therapy.
OptumRx, part of the UnitedHealth Group, has added RedHill Biopharma’s Talicia (omeprazole magnesium, amoxicillin and rifabutin) to its commercial formulary as an unrestricted brand for H. pylori treatment, effective July 1, 2021.
This decision extends U.S. health care coverage for Talica to more than 26 million Americans, according to officials from RedHill. “This listing represents the understanding within the medical community of the need to combat the high and growing resistance of H. pylori to commonly used antibiotics with an effective new first-line treatment,” Rick Scruggs, RedHill’s chief commercial officer, said in a statement.
Talicia is a fixed-dose, all-in-one oral capsule combination of two antibiotics (amoxicillin and rifabutin) and a proton pump inhibitor (PPI) (omeprazole). In November 2019, the FDA approved Talicia for the treatment of H. pylori infection in adults. In the pivotal phase 3 study, Talicia demonstrated 84% eradication of H. pylori infection in the intent-to-treat (ITT) group vs. 58% in the active comparator arm. This study also showed that patients in the trial who were confirmed adherent to their therapy had response rates of 90.3% in the Talicia arm vs. 64.7% in the active comparator arm.
Chronic gastritis caused by H. pylori infection can lead to increased risk of stomach cancer, according to the World Health Organization. Stomach cancer is the fourth most common cancer worldwide and the second most common cause of cancer death globally, according to the National Cancer Institute.
Navitus to Offer Unbranded Stelara Biosimilar, Remove Stelara from Formulary
March 13th 2025Lumicera Health Services, Navitus’ specialty pharmacy, has made a deal with Teva to offer an unbranded biosimilar that they estimate will save $112,000 and $336,000 per patient per year. Navitus will remove Stelara from formulary on July 1, 2025.
Read More
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More