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Cushing’s syndrome

PharmaDeviceNews Cushing’s syndrome
Endogenous Cushing’s syndrome research advances as the US Food and Drug Administration grants orphan drug designation to Lundbeck’s asedebart, supporting development of a novel ACTH-neutralising therapy for patients with rare endocrine disorders. Representative image.
Pharma & Biotech

Lundbeck wins FDA Orphan Drug status for asedebart in endogenous Cushing’s syndrome

FDA grants orphan status to Lundbeck’s asedebart for endogenous Cushing’s syndrome as Phase 2 testing examines direct ACTH neutralization.

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Representative image: Corcept Therapeutics has resubmitted the relacorilant New Drug Application for Cushing’s syndrome, reopening FDA scrutiny of efficacy, trial design and liver safety evidence.
Pharma & Biotech

Corcept revives its Cushing’s bid with relacorilant, yet the hardest evidence gap remains

Read how Corcept’s relacorilant NDA resubmission could reshape Cushing’s treatment while efficacy and liver safety questions remain.

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Representative image of clinical diabetes data review, highlighting Corcept’s Korlym findings in hypercortisolism-linked type 2 diabetes and GLP-1 treatment outcomes.
Pharma & Biotech

Corcept’s Korlym data put hypercortisolism back in focus for cardiometabolic disease

Read how Corcept’s ADA data could reshape hypercortisolism screening in difficult-to-control type 2 diabetes and GLP-1 care.

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Medical Devices & Diagnostics

Corcept Therapeutics expands hypercortisolism evidence base with largest US resistant hypertension screening trial

Corcept's MOMENTUM trial finds hypercortisolism in 27.3% of resistant hypertension patients. Explore what this means for screening and treatment. Read more.

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Pharma & Biotech

Corcept’s relacorilant CRL leaves endocrinology ambitions in limbo as oncology pivot takes center stage

Find out why FDA’s complete response letter for Corcept’s relacorilant could reshape treatment of hypercortisolism, with implications for oncology approval.

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