Evidence memo / Reproductive & endocrine

Pasireotide

Also: Signifor · Signifor LAR

Pasireotide (Signifor) is a multi-receptor somatostatin analog approved for Cushing's disease when surgery is not an option or has not worked, and for acromegaly. It lowers the hormone output driving those conditions. A notable concern is that it raises blood sugar more than other somatostatin analogs. The Watchlist boundary is keeping it to its specific endocrine indications and noting its strong effect on glucose.

Approved for specific usesApproved specific useSafety / regulatory watch

The verdict

Our read at a glance.

Whether pasireotide's approved Cushing's disease and acromegaly uses are understood within those specific indications and their metabolic trade-offs, rather than generalized.

The signal
Randomized trials support pasireotide for lowering cortisol in Cushing's disease and growth hormone and IGF-1 in acromegaly. Across trials, high rates of hyperglycemia and new or worsened diabetes are a consistent finding.
The unknown
How to balance its hormone-lowering benefit against its strong tendency to raise blood sugar, and where it fits relative to surgery and other medical options.
Our read
A targeted option for serious hormone-excess conditions, defined as much by its glucose side effect as its benefit. Pasireotide works on the underlying hormone problem in Cushing's disease and acromegaly, but its strong tendency to raise blood sugar is central to using it.

The mechanism

How it works.

Pasireotide is a synthetic somatostatin analog that binds a wider range of somatostatin receptor subtypes than older drugs like octreotide, hitting SSTR5 strongly in addition to SSTR2. In Cushing's disease that broad binding shuts down ACTH release from pituitary tumor cells, which lowers cortisol, and in acromegaly it suppresses growth hormone. The same receptor profile suppresses insulin release from the pancreas, so it raises blood sugar more than other analogs.

Safety & regulatory boundary

The consequential part.

Pasireotide commonly causes hyperglycemia and can lead to new or worsened diabetes, and it also carries gallbladder, heart-rhythm (QT), and liver-related cautions. It is approved for specific endocrine indications, and the subcutaneous and long-acting products are not interchangeable. Approved products are not the same as compounded or research-labeled pasireotide, and the approved uses do not extend to general wellness claims.

What's next

What we're watching.

Long-term metabolic safety, comparative data against other Cushing's and acromegaly treatments, and strategies to manage its glucose effects.

Context

Why this is discussed.

Pasireotide is one of the few medical options for Cushing's disease that targets the underlying hormone excess, so it matters in a hard-to-treat condition.

The evidence base

22 cited references.

Regulatory & labels2

DailyMed label: Signifor

Recordati Rare Diseases, Inc. (FDA label) · 2026

DailyMed label: Signifor LAR

Recordati Rare Diseases, Inc. (FDA label) · 2024

Indexed literature (PubMed)12

Acromegaly

Colao A et al. · Nat Rev Dis Primers · 2019

The Treatment of Cushing's Disease

Pivonello R et al. · Endocr Rev · 2015

Dumping syndrome: Update on pathophysiology, diagnosis, and management

Tack J et al. · Neurogastroenterol Motil · 2025

Somatostatin Analogs in Clinical Practice: a Review

Gomes-Porras M et al. · Int J Mol Sci · 2020

Pasireotide

PubMed · 2012

Consensus on acromegaly therapeutic outcomes: an update

Melmed S et al. · Nat Rev Endocrinol · 2025

Resistant prolactinomas

Samson SL · Best Pract Res Clin Endocrinol Metab · 2026

Aggressive prolactinoma (Review)

Valea A et al. · Exp Ther Med · 2022

Keep reading

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