Approved Therapeutic

Octreotide

Sandostatin · Sandostatin LAR

Octreotide is an approved peptide-based therapeutic or diagnostic asset. Product-specific labels define its validated uses and risks.

Compare
EvidenceTier 1
RegulatoryApproved
SafetyKnown but Manageable Risks
Clinical phaseApproved
01

Overview

ClassCyclic somatostatin analogue
Sponsor / developerMultiple manufacturers
Review statusReviewed
Record IDPEP-007
02

Plain-language guide

What it was designed or studied for

Designed and approved for specific uses that include Acromegaly, Carcinoid syndrome, VIPoma.

How it works, simply

It copies somatostatin, a braking signal that can reduce the release of selected hormones.

This simplified explanation is educational context, not a treatment recommendation or a substitute for the clinical evidence below.
03

Clinical mechanism

Binds somatostatin receptors and suppresses selected endocrine secretions.

Mechanism plausibility is not the same as demonstrated clinical benefit.
04

Applications

  • Acromegaly
  • Carcinoid syndrome
  • VIPoma
05

Human evidence

Multiple human studies and regulatory review support at least one product-specific indication.

Tier 1
06

Preclinical evidence

Mechanistic and preclinical findings are tracked separately and are not treated as proof of human clinical benefit.

06

Regulatory status

Approved. Regulatory status is product- and jurisdiction-specific and does not automatically follow from an evidence score.

07

Safety

Known but Manageable Risks

  • Adverse effects vary by product and indication
  • Contraindications and interactions require label review
08

Interactions

Review the current product label and indication-specific literature for pharmacologic and absorption interactions.

09

Treatment pattern

Treatment patterns are product-, indication- and clinician-specific; this educational profile does not provide dosing guidance.

10

Manufacturing and quality

Approved-product identity, formulation and quality controls must not be extrapolated to compounded or RUO copies.

12

Sources

  1. 01
    Primary regulatory record

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

  2. 02
    Clinical trial registry

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

  3. 03
    Peer-reviewed literature

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

13

Gaps and unverified claims

  • Evidence must be interpreted by indication and product label.
  • Approval does not establish safety or efficacy for off-label or compounded copies.
14

Last reviewed

August 5, 2026 · Reviewed