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FDA Approves Brodalumab Drug for Psoriasis Treatment

by Madhumathi Palaniappan on February 20, 2017 at 11:22 AM
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Highlights

The United States Food and Drug Administration (USFDA) has approved Brodalumab drug for the treatment of moderate-to-severe plaque psoriasis.


Psoriasis is an autoimmune disease which causes redness and scaly patches on the skin. Plaque psoriasis is the most common type of psoriasis and is responsible for 80% of the total cases.

‘The Food and Drug Administration (FDA) has approved brodalumab drug for the treatment of plaque psoriasis.’

Brodalumab drug (Siliq) is administered as an injection. The drug is intended for systemic therapy using substances which can travel through the bloodstream after taking the injection, or ultraviolet therapy and have failed to respond or stopped responding to the other therapies.

Julie Beltz, M.D., director of the Office of Drug Evaluation III in the FDA's Center for Drug Evaluation and Research, said, "Moderate-to-severe plaque psoriasis can cause significant skin irritation and discomfort for patients, and today's approval provides patients with another treatment option for their psoriasis."

"Patients and their health care providers should discuss the benefits and risks of brodalumab drug before considering treatment."

Brodalumab - Mechanism of Action
The active ingredient of the drug mainly acts by binding to a protein which causes inflammation and inhibits the inflammatory response which plays a role in plaque psoriasis.

Clinical Trial
The efficacy and safety of brodalumab drug were established in three randomized, placebo-controlled clinical trial on 4,373 participants who have moderate-severe plaque psoriasis who were eligible for systemic therapy or phototherapy.

The results of the clinical trial conducted on patients who took brodalumab drug were compared to the patients who took placebo. More number of patients who took brodalumab drug were found to have a clear or almost clear skin when compared to the placebo. This was assessed by scoring the extent, nature and severity of the skin changes.

Risk of Suicidal Ideation and Behavior
The patients who were treated with brodalumab drug in clinical trials had a risk of suicidal ideation and behavior. These users with a history of suicidality or depression may further have an increased risk of suicidal ideation or behavior.

Due to the observed risk, the labeling for brodalumab drug includes a boxed warning and the drug can be available only through the Risk Evaluation and Mitigation Strategy (REMS)

The requirements of the Brodalumab Risk Evaluation and Mitigation Strategy (REMS) Program include

Common Side Effects of Brodalumab Drug

The drug is approved along with a medication guide which informs the patient about the risk of suicidal ideation and behavior. The drug may also affect the immune system and may have an increased risk of acquiring infection.

Note: The drug must not be injected to patients who have active tuberculosis infections.

They must avoid immunizations with live vaccines when treated with brodalumab drug

Facts on Psoriasis

References

  1. About Psoriasis - (https:www.psoriasis.org/about-psoriasis)
  2. FDA approves new psoriasis drug - (https:www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm541981.htm)


Source: Medindia

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