RECORDATI SUBMITS NEW DRUG APPLICATION FOR ISTURISA® IN
The JNDA for osilodrostat is primarily based on data generated by the clinical program which included Japanese patients. In the Phase 3 LINC‐3 study, a significantly higher proportion of patients treated with Isturisa® (osilodrostat) maintained normal mean urinary free cortisol (mUFC) at the end of the 8‐week randomized withdrawal period (week 34) versus placebo (86.1% vs 29.4%). The safety profile was manageable.
“We are excited about this regulatory filing for osilodrostat in
About Cushing’s Syndrome
Cushing’s syndrome is a rare, chronically debilitating, life-threatening condition. The primary clinical symptoms of Cushing’s syndrome are due to hypercortisolism and include the following: changes in body habits due to increased fat accumulation; hirsutism; skin changes with easy bruising, purplish striae, reddening and ulceration of the cheeks; generalized weakness and fatigue; wasting of musculature; menstrual disorders in females; decreased fertility and/or libido; hypertension; weight gain; increased insulin resistance with alterations in glucose metabolism; dyslipidemia; depression, mood and behavior disorders; sleep disturbances and osteopenia/osteoporosis.
Hypercortisolism is the main driving force of morbidity and mortality in patients with Cushing’s syndrome, therefore, potent inhibition of cortisol synthesis (and the resulting normalization of cortisol levels) has the potential to ameliorate the complications of this debilitating group of disorders.
About Isturisa®
Isturisa® ( osilodrostat) is a cortisol synthesis inhibitor that works by preventing 11‐betahydroxylase, an enzyme responsible for the final step of cortisol biosynthesis in the adrenal gland, from being created. Given the mechanism of action to inhibit cortisol synthesis at the adrenal glands, osilodrostat has therapeutic potential in all forms of endogenous Cushing syndrome.
About Recordati Rare Diseases K.K.
Recordati Rare Diseases K.K. is a biopharmaceutical company committed to providing often-overlooked orphan therapies to the underserved rare disease communities in
Recordati Rare Diseases' mission is to reduce the impact of extremely rare and devastating diseases by providing urgently needed therapies. We work side-by-side with rare disease communities to increase awareness, improve diagnosis and expand availability of treatments for people with rare diseases.
For a full list of our Japanese products please click here: https://www.recordati.com/en/international_presence/japan
The company's Japanese headquarters is located in
About Recordati
Recordati, established in 1926, is an international pharmaceutical group, listed on the
For further information:
Recordati website: www.recordati.com
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Marianne Tatschke Studio Noris Morano
(39)0248787393 (39)0276004736, (39)0276004745
e-mail: investorelations@recordati.it e-mail: norismorano@studionorismorano.com
Statements contained in this release, other than historical facts, are "forward-looking statements" (as such term is defined in the Private Securities Litigation Reform Act of 1995). These statements are based on currently available information, on current best estimates, and on assumptions believed to be reasonable. This information, these estimates and assumptions may prove to be incomplete or erroneous, and involve numerous risks and uncertainties, beyond the Company’s control. Hence, actual results may differ materially from those expressed or implied by such forward-looking statements. All mentions and descriptions of Recordati products are intended solely as information on the general nature of the company’s activities and are not intended to indicate the advisability of administering any product in any particular instance.
Attachment
- Isturisa filing
Japan
Source: RECORDATI
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