ClinicalTrials.gg
Drug

Motexafin lutetium clinical trials

Also written PCI-0123 and lutetium texaphyrin.

studies test it
3
open now
0
in phase 3
0
first study started
2000

How each study uses motexafin lutetium is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study

Approvals

The first approval found in each region, with its record

United States
Not in FDA's approval records
European Union
Not in EMA's list of EU-wide authorisations

From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out

How studies write it

Studies that test it under each name

Name

motexafin lutetium
3
Antrin
3
lutetium texaphrin
3
Lutex
3

Development codes

PCI-0123
3

Other names

lutetium texaphyrin
3

Studies by the year they started

3 studies that test it; most in 2000 (2)

Studies that test motexafin lutetium, by start year
YearStudies
20002
20041

By phase

A phase 1/2 study counts in both.

Phase 1
2
No phase
1

What it is tested for

Each study’s main condition, where its own words name it, so a study counts once.

Who runs them

Industry 0 · Other 3

National Cancer Institute (NCI) (3)

Often tested with

Tested in the same studies.

EF-5 (1) · Photodynamic Therapy (1)

Studies

Open first, then newest update. How each study uses motexafin lutetium is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.

Testing it · 3

Codes

What other systems call motexafin lutetium · ClinicalTrials.gg INT003946

  • MeSH (NLM) C102825motexafin lutetiumConfirmed ClinicalTrials.gov, NLM
  • UNII (FDA) 0A85BJ22L6MOTEXAFIN LUTETIUMConfirmed FDA, NLM
  • NCI Thesaurus C1651Motexafin LutetiumOne source FDA

“Confirmed” means two independent publishers link the code to this drug; “one source”, one does and its name agrees.