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NCT01377532

Compassionate Use of 131I-MIBG for Patients With Malignant Pheochromocytoma

APPROVED FOR MARKETING Last updated 6 May 2020
What this trial tests

trial testing 131 I-Metaiodobenzylguanidine (131 I-MIBG) in Pheochromocytoma. Approved for marketing.

Quick facts

Lead sponsorUniversity of California, San Francisco
StatusAPPROVED FOR MARKETING
Study typeEXPANDED_ACCESS
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, San Francisco

Who can join

2 and older, any sex, with Pheochromocytoma or Paraganglioma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a compassionate use protocol to allow palliative therapy for patients with malignant pheochromocytoma and paragangliomas.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Pediatric Metastatic Pheochromocytoma and Paraganglioma: Clinical Presentation and Diagnosis, Genetics, and Therapeutic Approaches.
    Kuo MJM, Nazari MA, Jha A, Pacak K. · · 2022 · cited 19× · PMID 35903274 · DOI 10.3389/fendo.2022.936178

Verify or expand the search:

Other trials of 131 I-Metaiodobenzylguanidine (131 I-MIBG)

Trials testing the same drug.

Other recruiting trials for Pheochromocytoma

Currently open trials in the same condition.

Other University of California, San Francisco trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01377532.

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