ClinicalTrials.gg
Drug

Lucinactant clinical trials

Also written SURFAXIN®.

studies test it
4
open now
0
in phase 3
1
first study started
2000

How each study uses lucinactant 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
6 Mar 2012 · SURFAXIN · NDA 021746 (FDA, Drugs@FDA)
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

Lucinactant
4
Surfactant
3

Brand

SURFAXIN®
2

Studies by the year they started

4 studies that test it; most in 2000 (1)

Studies that test lucinactant, by start year
YearStudies
20001
20051
20071
20211

By phase

A phase 1/2 study counts in both.

Phase 2
3
Phase 3
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 4 · Other 0

Windtree Therapeutics (4)

Studies

Open first, then newest update. How each study uses lucinactant 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 · 4

Codes

What other systems call lucinactant · ClinicalTrials.gg INT004801

  • UNII (FDA) 5BSH2G9BH8LUCINACTANTOne source FDA
  • RxNorm 1293254One source FDA
  • NCI Thesaurus C172611LucinactantOne source FDA

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