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NCT04943211: HISTIOGEN
Determination of Molecular Status, the Efficacy and Safety of Fluorodeoxyglucose in PET-CT Imaging
Phase 3 trial testing fluorodeoxyglucose (18F-FDG) in Histiocytosis in 150 participants. Currently enrolling.
30 June 2027
Quick facts
| Lead sponsor | Anna Raciborska |
|---|---|
| Phase | Phase 3 |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 150 |
| Start date | 1 April 2021 |
| Primary completion | 30 June 2027 |
| Estimated completion | 30 June 2027 |
| Sites | 1 location across Poland |
Drugs / interventions tested
- fluorodeoxyglucose (18F-FDG) — full drug profile →
Conditions studied
- Histiocytosis — all drugs for Histiocytosis →
Sponsor
Anna Raciborska — full company profile →
Who can join
Adults 1 to 18, any sex, with Histiocytosis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Prospective, low intervention, open, single-center, non-commercial clinical trial to improve diagnostics in patients with histiocytosis by assessing the molecular profile of the tumor tissues, monitoring its presence in free-circulating DNA, and determining the efficacy of fluorodeoxyglucose (18F-FDG) in PET-CT imaging.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04943211
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Histiocytosis
Currently open trials in the same condition.
- NCT04943224 — Optimization of the Time and Dosage of Trametinib in BRAF Negative Juvenile Patients · Phase 2 · recruiting
- NCT04943198 — Optimization of the Time and Dosage of Vemurafenib in BRAF Positive Juvenile Patients With Refractory Histiocytosis · Phase 2 · recruiting
- NCT04665674 — Adult Pulmonary Langerhans Cell Histiocytosis: a National Registry-based Prospective Cohort Study · recruiting
Other Anna Raciborska trials
Trials by the same sponsor.
- NCT05968768 — To Evaluate the Efficacy and Safety of Naxitamab in Patients With Refractory Ewing's Sarcoma (Butterfly) · Phase 2 · recruiting
- NCT04943224 — Optimization of the Time and Dosage of Trametinib in BRAF Negative Juvenile Patients · Phase 2 · recruiting
- NCT04943198 — Optimization of the Time and Dosage of Vemurafenib in BRAF Positive Juvenile Patients With Refractory Histiocytosis · Phase 2 · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04943211 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Anna Raciborska
- Last refreshed: 25 March 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04943211.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing