CT-P10 clinical trials
A product of Rituximab; its studies count on that page too.
How each study uses CT-P10 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
- 26 Nov 1997 · RITUXAN · BLA 103705 (FDA, Drugs@FDA; as Rituximab)
- European Union
- 2 Jun 1998 · MabThera · EMEA/H/C/000165 (EMA; as Rituximab)
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
Studies by the year they started
3 studies that test it; most in 2014 (2)
| Year | Studies |
|---|---|
| 2014 | 2 |
| 2015 | 1 |
By phase
A phase 1/2 study counts in both.
- Phase 3
- 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
Related medicines
As reviewed, each with the page that says it.
- A biosimilar of Rituximab
Studies
Open first, then newest update. How each study uses CT-P10 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
- PK Similarity Prospective Phase 3 Study in Patients With Rheumatoid ArthritisCompletedPhase 3CelltrionNCT02149121Written as CT-P10
- To Compare Efficacy and Safety Between CT-P10 and Rituxan in Patients With Low Tumour Burden Follicular LymphomaCompletedPhase 3CelltrionNCT02260804Written as CT-P10
- To Demonstrate Equivalence of Pharmacokinetics and Noninferiority of Efficacy for CT-P10 in Comparison With RituxanCompletedPhase 3CelltrionNCT02162771Written as CT-P10