Compound library / Research / Investigational

Octreotide (Sandostatin)

Long-acting somatostatin analogue that suppresses GH, IGF-1, glucagon, and insulin secretion; FDA-approved for acromegaly and carcinoid tumors, but explored in biohacking circles for IGF-1 modulation and cancer-adjacent protocols.

CategoryResearch / Investigational
Regulatory standingNo approved product cited
Typical routeSubcutaneous
Half-life~1.7-1.9 hours (immediate-release); LAR depot effective ~4 weeks
Common dose range50-200 mcg SC 3x/day (immediate-release); 10-30 mg/month IM (LAR)
Typical cycle lengthPer clinical indication; not established for non-clinical use

BioHack Track models Octreotide (Sandostatin) at a half-life of 1.8 hours, so every dose you log is decayed against that curve and the app shows estimated active levels — not just what you typed.

No approved product cited

No FDA-approved product for this compound is cited on this page, and no approved human dose is quoted. Treat the range below as research and community practice rather than a prescribed dose.

Reconstitution

Immediate-release: supplied in pre-filled syringes. LAR: requires reconstitution with provided diluent at clinic.

Storage

Refrigerate.

Cautions

Prescription medication. Suppresses multiple hormones including thyroid and GI hormones, causing GI side effects, gallstones, and blood glucose dysregulation. Not for self-administration outside clinical guidance.

Track Octreotide (Sandostatin) in BioHack Track. Half-life, dose range and route come pre-filled from this library — log a dose and the app counts your vial down, models what is in your system, and puts it on the same chart as your labs and body composition.

Others in Research / Investigational

Look up the research

These open a search of each database for Octreotide (Sandostatin) — they are not citations, and nothing here is evidence for any particular dose. The same links are in the app.

Work it out

Where these figures come from

The half-life, route and dose range on this page are compiled from published pharmacokinetic literature, manufacturer and product monographs where one exists, and the ranges commonly reported in clinical and research use. They are kept as a range rather than a single figure because that is what the sources actually support — a half-life varies with route, formulation and the person.

These are not citations, and this page is not a review of the evidence. Where a number matters to you, follow the database links above and read the source. We say so plainly rather than dressing a compiled reference up as one.

Nothing on this page has been reviewed by a named clinician. It is a reference for people already tracking a protocol, not a recommendation to start one.

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