|Articles|April 21, 2017

Valeant Announces List Price of Brodalumab

Valeant’s Siliq (brodalumab) injection will be listed for $3500 a month in the United States, the company said on April 21, 2017. In a statement, Valeant said this makes Siliq the lowest-priced injectable biologic to treat psoriasis on the US market.

Valeant’s Siliq (brodalumab) injection will be listed for $3500 a month in the United States, the company said on April 21, 2017. In a statement, Valeant said this makes Siliq the lowest-priced injectable biologic to treat psoriasis on the US market. In an emailed statement to BioPharm International a spokesperson for the company said it "compared the list prices of all the injectable psoriasis treatments on the market today in the United States and factored in all of the varying dosages for the treatments" in order to make this determination. A Valeant spokesperson also told this publication the per dose wholesale acquisition cost for Siliq is $1750 for one syringe, not including discounts and rebates. 

Siliq received FDA approval in February 2017 as a treatment for moderate-to-severe plaque psoriasis. The drug comes with a boxed warning for its potential link to suicidal ideation. During clinical trials, some patients treated with Siliq succeeded in committing suicide, FDA noted in a press release announcing the drug’s approval. In May 2015, Amgen dropped out of co-developing Siliq with AstraZeneca after news of the drug’s association to suicidal ideation in clinical trials. Valeant took over commercialization and development of the drug in the US later that year.

It is likely that Siliq will be a competitive psoriasis treatment. The drug is an IL-17 inhibitor, and has demonstrated improved plaque clearance when compared with anti-tumor necrosis factor therapies. The drug is expected to be available for sale in the US during the second half of 2017. 

*This article was updated on April 24, 2017 to include comments from Valeant

Source: Valeant


Related to this article

The BioPharm Brief: Survival, Gene Editing, and Skin Cancer
This episode of the BioPharm Brief highlights Roche’s Tam-Peli phase 3 survival data in relapsed small-cell lung cancer, Cellectis’ shift to in vivo gene editing for lipid disorders, and Phio Pharmaceuticals’ FDA briefing package for PH-762 in cutaneous squamous cell carcinoma.
Stainless steel bioreactor vessels in a manufacturing facility. | Image Credit: © Corona Borealis - stock.adobe.com
Four cell therapy developers have pulled back from ex vivo manufacturing in the past month — ArsenalBio, TScan Therapeutics, and Cellectis all pivoted to in vivo approaches, while Bristol Myers Squibb terminated its manufacturing partnership with automation specialist Cellares after determining its platform couldn't meet requirements for commercial Breyanzi production, triggering layoffs.