EMA approves Signifor as Cushing's disease treatment

By Admin
The European Medicines Agency (EMA) has approved the Novartis drug Signifor as the first medication to treat Cushings disease. Signifor has been approv...

The European Medicines Agency (EMA) has approved the Novartis drug Signifor as the first medication to treat Cushing’s disease.

Signifor has been approved for use in adult patients with Cushing’s disease, particularly for those for which surgery either is not a feasible option, or has failed.

The approval is based on data from the largest randomized Phase III study to evaluate a medical therapy in patients with Cushing's disease.

To read the latest edition of Healthcare Global, click here

Cushing’s disease is a very rare hormonal disorder which is caused when an underlying tumour on the pituitary gland triggers the production of excess cortisol.

As a result, this can cause weight gain and an increase in blood pressure, along with depression, anxiety, fatigue and weakness.  

Signifor works by reducing the levels of cortisol in the patients’ bodies.

It was discovered that with reduced cortisol levels, key clinical manifestations of the disease improved, which included a reduction in blood pressure, cholesterol, weight and body mass index (BMI).

Commenting on the approval of Signifor, the President of Novartis Oncology, Hervé Hoppenot, said: “As the first therapeutic option to specifically target Cushing's disease, Signifor has the potential to redefine treatment of this debilitating disease.

“By focusing research efforts on our understanding of this rare disease where there is significant unmet need, we have been able to successfully bring a novel treatment option to patients in the European Union.”

Meanwhile, Ellen van Veldhuizen, a board member of the Dutch Adrenal Society, added: “Patients with Cushing's disease often struggle with a variety of debilitating health issues associated with the overproduction of cortisol and previously were faced with a treatment approach limited to surgery.

“The approval of pasireotide as a new treatment option that may help patients with Cushing's disease is welcome news.”

Cushing’s disease is most common in adults aged between 20 and 50 years old and is three more times common in women than it is in men.

The EMA’s approval of Signifor is more welcome news for Novartis, which only last week had its treatment for multiple sclerosis, Gilenya, approved for continued use.

The Healthcare Global magazine is now available on the iPad. Click here to download it.


Featured Articles

Cardinal Health’s clinically integrated pharma supply chain

Peter Siavelis, SVP & General Manager, Health System and Provider Distribution & Services at Cardinal Health, discusses the integrated pharma supply chain

Healthcare Digital news roundup: digital healthcare & AI

This week in Healthcare Digital, we looked at digital skills for healthcare leaders, medical technology & acoustic AI used in digital cough monitoring

Hospitals must embrace IoMT device security

As cybersecurity threats rise in the healthcare sector, hospitals must get serious about IoMT device protection, says Shankar Somasundaram, CEO of Asimily

Mental health support for working women and mothers

Digital Healthcare

Digital evolution delivers better healthcare outcomes

Digital Healthcare

Hyfe AI uses acoustic AI in its digital cough monitoring

Technology & AI