Ozmosi | Pertechnetate Drug Profile
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Pertechnetate

Pronounced as: per-TEK-ne-tate

Alternative Names: pertechnetate, minitec, technelite, ultra-technekow fm, radiogenix system
Clinical Status: Active
Latest Update: 2026-01-13
Latest Update Note: News Article

Product Description

A gamma-emitting radionuclide imaging agent used for the diagnosis of diseases in many tissues, particularly in the gastrointestinal system, cardiovascular and cerebral circulation, brain, thyroid, and joints. (Sourced from: https://pubchem.ncbi.nlm.nih.gov/compound/Pertechnetate)

Mechanisms of Action: No Mechanism

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Approved

Approved Countries: Australia | Austria | Belgium | Bosnia | Brazil | Bulgaria | Canada | China | Colombia | Croatia | Czech | Denmark | Dominican Republic | Estonia | Finland | France | Greece | Hong Kong | Hungary | Ireland | Italy | Korea | Latvia | Lithuania | Luxembourg | Malaysia | Malta | Netherlands | Norway | Poland | Portugal | Romania | Russia | Serbia | Singapore | Slovakia | Slovenia | Spain | Sweden | Switzerland | Taiwan | Turkey | Ukraine | Vietnam

Approved Indications: None

Known Adverse Events: None

Company: IIS LA FE
Company Location: Europe
Company Founding Year: 2013
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Pertechnetate

Countries in Clinic: Spain

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Ovarian Cancer

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2024-520189-67-00

SENTOV II

P3

Not yet recruiting

Ovarian Cancer

2028-06-02