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Pertechnetate

Alternative Names: pertechnetate, minitec, technelite, ultra-technekow fm, radiogenix system
Latest Update: 2024-11-19
Latest Update Note: Clinical Trial Update

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: None *

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: Fundacio De Recerca Clinic Barcelona-Institut D’investigacions Biomediques August Pi I Sunyer
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Pertechnetate

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 4: Other

Phase 3: Bone Cancer

Phase 2: COVID-19|Pneumonia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2024-518974-15-01

P4

Unknown Status

Other

2030-05-15

2021-006371-42

P4

Active, not recruiting

Unknown

2027-01-18

SOLLID

N/A

Completed

Other

2022-06-30

99mTC thyroid scan in DTC

N/A

Unknown status

Thyroid Cancer

2021-12-31

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