Last reviewed · How we verify

OCTREOSCAN (INDIUM IN-111 PENTETREOTIDE KIT)

CURIUM · FDA-approved approved ✓ Verified May 2026

OCTREOSCAN (generic name: INDIUM IN-111 PENTETREOTIDE KIT) is a drug developed by CURIUM. It is currently FDA-approved.

OCTREOSCAN, also known as Yttrium Y 90-edotreotide, is used to treat various conditions including Breast Cancer, Lung Cancer, Sarcoidosis, Solid Tumors, and Neuroendocrine Carcinoma. It is a radiolabeled compound that contains Yttrium Y 90, which is attached to the peptide edotreotide.

At a glance

Generic nameINDIUM IN-111 PENTETREOTIDE KIT
SponsorCURIUM
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about OCTREOSCAN

What is OCTREOSCAN?

OCTREOSCAN (INDIUM IN-111 PENTETREOTIDE KIT) is a pharmaceutical drug developed by CURIUM.

Who makes OCTREOSCAN?

OCTREOSCAN is developed and marketed by CURIUM (see full CURIUM pipeline at /company/curium).

What is the generic name of OCTREOSCAN?

INDIUM IN-111 PENTETREOTIDE KIT is the generic (nonproprietary) name of OCTREOSCAN.

What development phase is OCTREOSCAN in?

OCTREOSCAN is FDA-approved (marketed).

What are the side effects of OCTREOSCAN?

Common side effects of OCTREOSCAN include Nausea, Injection site pain, Diarrhea, Abdominal pain/discomfort, Loose stools, Vomiting. Serious adverse events: Bradycardia, Decreased hematocrit, Decreased hemoglobin, Angioedema.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing