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Temoporfin

Alternative Names: temoporfin, foscan
Latest Update: 2024-04-04
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: Free Radical Inducer

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Austria | Belgium | Croatia | Czech | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hungary | Iceland | India | Ireland | Italy | Latvia | Lithuania | Netherlands | Poland | Portugal | Slovakia | Spain | Sweden | United Kingdom

Approved Indications: None

Known Adverse Events: None

Company: Quintiles IMS
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Temoporfin

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 4: Cholangiocarcinoma

Phase 2: Nasopharyngeal Cancer|Squamous Cell Carcinoma|Ductal Carcinoma|Head and Neck Cancer|Oncology Unspecified|Cholangiocarcinoma|Klatskin Tumor

Phase 1: Non-Small-Cell Lung Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

CARP

P4

Recruiting

Cholangiocarcinoma

2027-12-31

PDT

P2

Completed

Cholangiocarcinoma|Klatskin Tumor

2023-04-12

I 228112

P1

Completed

Non-Small-Cell Lung Cancer

2018-09-04

NCT01637376

P1

Withdrawn

Non-Small-Cell Lung Cancer

2014-01-01

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