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Tzield, the World's First USFDA approved drug to delay type 1 diabetes onset to cost more than Rs 11 lakh per vial, confirm makers

Ruchika SharmaWritten by Ruchika Sharma Published On 2022-11-19T11:49:42+05:30  |  Updated On 19 Nov 2022 11:49 AM IST
Tzield, the Worlds First USFDA approved drug to delay type 1 diabetes onset to cost more than Rs 11 lakh per vial, confirm makers
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New Jersey: With the recent USFDA, approval of the first drug to delay type 1 diabetes onset, teplizumab, makers of the drug Provention Bio Inc on Friday its stated that the drug sold under the brand name Tzield would cost $13,850 a vial ( Rs 11,29,054 approximately).

Medical Dialogues drug had recently reported that the U.S. Food and Drug Administration approved the use of the drug, to be sold under the brand name Tzield, late on Thursday for delaying the onset of insulin-dependent type 1 diabetes, which is less common than type 2 of the disease, for people aged 8 years and above.
This comes in the wake of the clinical trial, TZIELD delayed the median onset of Stage 3 T1D by 25 months or approximately two years in patients with stage 2 T1D, compared to placebo. Stage 3 T1D is linked with significant health risks, including diabetic ketoacidosis, which can be life-threatening. In due course, patients who progress to Stage 3 T1D need insulin injections for life.

Tzield binds to specific immune system cells and delays progression to stage 3 type 1 diabetes. It may deactivate the immune cells that attack insulin-producing cells and increase the proportion of cells that help moderate the immune response. The administration of Tzield is via intravenous (IV) infusion once daily for 14 consecutive days.

A 14-day regimen of the drug would translate to a price of $193,900, the company said on a conference call.

In October, Provention signed a co-promotion deal for the drug with Sanofi, offering the French drugmaker first negotiation for exclusive global rights to commercialize the drug in exchange for an upfront payment of $20 million.
As per the deal, the approval also allows Sanofi to purchase up to $35 million of Provention's common shares.
Read also: Sanofi, Provention Bio ink pact for launch of Diabetes drug Teplizumab

What is Tzield (teplizumab) ?

TZIELD (teplizumab-mzwv) is a CD3-directed antibody indicated to delay the onset of Stage 3 T1D in adults and pediatric patients aged 8 years and older with Stage 2 T1D. TZIELD injection is supplied as a sterile, preservative-free, clear and colorless solution in a 2 mg/2 mL (1 mg/mL) single-dose vial for intravenous use. TZIELD should be administered by intravenous infusion (over a minimum of 30 minutes) once daily for 14 days. Please see full prescribing information for the dosing schedule.

Tzield's safety and efficacy were evaluated in a randomized, double-blind, event-driven, placebo-controlled trial with 76 patients with stage 2 type 1 diabetes. In the trial, patients randomly received Tzield or a placebo once daily via intravenous infusion for 14 days. The primary measure of efficacy was the time from randomization to development of stage 3 type 1 diabetes diagnosis. The trial results showed that over a median follow-up of 51 months, 45% of the 44 patients who received Tzield were later diagnosed with stage 3 type 1 diabetes, compared to 72% of the 32 patients who received a placebo. The mid-range time from randomization to stage 3 type 1 diabetes diagnosis was 50 months for the patients who received Tzield and 25 months for those who received a placebo. This represents a statistically significant delay in the development of stage 3 type 1 diabetes.

The most common side effects of Tzield include decreased levels of certain white blood cells, rash and headache. The use of Tzield comes with warnings and precautions, including premedicating and monitoring for symptoms of Cytokine Release Syndrome; risk of serious infections; decreased levels of a type of white blood cell called lymphocytes; risk of hypersensitivity reactions; the need to administer all age-appropriate vaccinations prior to starting Tzield; as well as avoiding concurrent use of live, inactivated and mRNA vaccines with Tzield.

Provention BioProvention Bio newsdiabetes drugdiabetesteplizumabUSFDATzieldtype 1 diabetesSanofidiabetes drugs
Ruchika Sharma
Ruchika Sharma

    Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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