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Drug

PM 00104 clinical trials

Also written Zalypsis and PM00104.

studies test it
3
open now
0
in phase 3
0
first study started
2006

How each study uses PM 00104 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

Brand

Zalypsis
2

Development codes

PM00104
2

Studies by the year they started

3 studies that test it; most in 2006 (1)

Studies that test PM 00104, by start year
YearStudies
20061
20091
20101

By phase

A phase 1/2 study counts in both.

Phase 1
1
Phase 2
2

What it is tested for

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

Sarcoma, Ewing
1
Uterine Cervical Neoplasms
1
Lymphoma
1

Who runs them

Industry 3 · Other 0

PharmaMar (3)

Studies

Open first, then newest update. How each study uses PM 00104 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 PM 00104 · ClinicalTrials.gg INT004777

  • UNII (FDA) C21EZR41AYPM-00104Confirmed FDA, Wikidata
  • Wikidata Q27275078pm-00104Confirmed FDA, Wikidata
  • DrugBank DB12454One source Wikidata

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