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NCT01747512

A Phase II/III Study of Cyclotron-produced Tc-99m Pertechnetate (C-PERT) Efficacy and Safety in Patients With Conformed and Suspected Thyroid Cancer or Head and Neck Cancer

Withdrawn Phase 2 Last updated 10 November 2017
What this trial tests

Phase 2 trial testing C-PERT in Thyroid Neoplasms. Withdrawn.

Quick facts

Lead sponsorAHS Cancer Control Alberta
PhasePhase 2
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Primary completion1 May 2013

Drugs / interventions tested

Conditions studied

Sponsor

AHS Cancer Control Alberta — full company profile →

Who can join

Adults 18 to 79, any sex, with Thyroid Neoplasms or Head and Neck Neoplasms. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

Doctors at the Cross Cancer Institute have developed a new method of producing 99mTc Pertechnetate in a cyclotron unit. A study done at the Cross Cancer Institute in 2011 with ten patients using this imaging agent showed that it was safe and produced images with the same pattern as generator produced Pertechnetate. This study is now being done in larger numbers of patients to again show that the imaging pattern of both agents is the same, and to again demonstrate its safety.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Thyroid Neoplasms

Currently open trials in the same condition.

Other AHS Cancer Control Alberta 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/NCT01747512.

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