Provention Bio Chooses Amber as Specialty Pharmacy for Tzield
Tzield addresses the underlying cause of the disease, where the immune system destroys the insulin producing cells in the pancreas. It is administered by intravenous infusion once daily for 14 consecutive days.
Amber Specialty Pharmacy will be dispensing Provention Bio’s Tzield (teplizumab) to delay the onset of stage 3 type 1 diabetes. It is indicated for adults and pediatric patients 8 years and older who currently have stage 2 type 1 diabetes. Tzield is anti-CD3-directed antibody, and binds to CD3, a cell surface antigen present on T lymphocytes. Tzield is administered by intravenous infusion once daily for 14 consecutive days.
The specialty pharmacy, Hy-Vee subsidiary, has 19 locations with ambulatory and home infusion capabilities.
“Living with or caring for a child with type 1 diabetes requires constant daily management,” Kristin Williams, president of Amber Specialty Pharmacy, said in a press release. “We understand how important it is for at-risk individuals to have access to medication and reliable support in order to delay disease progression.
Related: FDA Approves First Drug that Delays Diabetes
The FDA approved Tzield last week. It will be available by the end of the year at a wholesale acquisition cost of $13,850 per vial for 14-day treatment course list price of $193,900, company executives said in a call with investors.
In October 2022 the company announced a co-promotion agreement for the U.S. launch of Tzield with Sanofi.
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
