MDX-1303 clinical trials
- studies test it
- 3
- open now
- 0
- in phase 3
- 0
- first study started
- 2009
How each study uses MDX-1303 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
Development codes
- MDX1303
- 1
Studies by the year they started
3 studies that test it; most in 2009 (2)
| Year | Studies |
|---|---|
| 2009 | 2 |
| 2010 | 1 |
By phase
A phase 1/2 study counts in both.
- Phase 1
- 3
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 3 · Other 0
PharmAthene, Inc. (3)
Studies
Open first, then newest update. How each study uses MDX-1303 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
- Dose Escalation Study of Valortim® (MDX-1303) Administered Intravenously (IV) in Healthy, Normal SubjectsCompletedPhase 1PharmAthene, Inc.NCT01265745Written as MDX1303
- Ph1 Study of Valortim and Ciprofloxacin in HumansSuspendedPhase 1PharmAthene, Inc.NCT00964561Written as Ciprofloxacin and Valortim
- Ph1 Study of Valortim and Doxycycline in HumansTerminatedPhase 1PharmAthene, Inc.NCT00964834Written as Doxycycline and Valortim