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Pasireotide

Aliases: Signifor

Last verified: 2026-09-23

Approved drugStrong evidencePeptidesMedium interest

The short version

A broader-spectrum somatostatin analogue (SSTR1/2/3/5) — approved for Cushing's disease and first-line-resistant acromegaly.

Identity & type

Molecular type
analog
Origin
A broader-spectrum somatostatin analogue (SSTR1/2/3/5) — approved for Cushing's disease and first-line-resistant acromegaly.

Mechanism of action

Broader SSTR profile → suppression of tumor ACTH/GH secretion.

Dosing & routes

Official / clinical context

Approved drug — indications, dosing and warnings are defined by the official label. SC 0.3–0.9 mg twice daily; LAR 10–40 mg monthly.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

SC 0.3–0.9 mg twice daily; LAR 10–40 mg monthly. Signifor: a broader somatostatin profile — lowers cortisol in Cushing's disease, but often raises glucose.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Signifor: a broader somatostatin profile — lowers cortisol in Cushing's disease, but often raises glucose.

Protocol — official vs community

Official / label

Signifor (Cushing's disease): 0.3–0.9 mg SC twice daily, titrated by urinary free cortisol. Signifor LAR (acromegaly after surgery or first-line somatostatin-analog failure): 10–40 mg IM every 4 weeks.

  1. 01Cushing's: start 0.6 mg SC BID; adjust in 0.3 mg steps by 24-h urinary free cortisol
  2. 02LAR acromegaly: start 40 mg q4wk; reduce to 10–20 mg if over-suppressed or intolerant

Duration: Chronic while biochemical control is needed; Cushing's response should be assessed within ~2 months before committing.

Its broader SSTR profile buys ACTH suppression that octreotide cannot deliver, at the price of markedly worse hyperglycemia — glucose monitoring is part of the protocol, not an afterthought.

Community (anecdotal)

Structured protocol data for this entry is coming.

Human evidence

Approved 2012/2014; unique for ACTH suppression.

Preclinical evidence

The preclinical phase was completed and submitted to regulators as part of registration; pharmacology and toxicology details are part of the official label.

Known risks

  • Hyperglycemia (common, significant), gallstones.characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Real-world data outside controlled trials

Frequently asked questions

References