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NCT04943211: HISTIOGEN

Determination of Molecular Status, the Efficacy and Safety of Fluorodeoxyglucose in PET-CT Imaging

Recruiting now Phase 3 Last updated 25 March 2026
What this trial tests

Phase 3 trial testing fluorodeoxyglucose (18F-FDG) in Histiocytosis in 150 participants. Currently enrolling.

Timeline
1 April 2021
Primary endpoint
30 June 2027
30 June 2027

Quick facts

Lead sponsorAnna Raciborska
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment150
Start date1 April 2021
Primary completion30 June 2027
Estimated completion30 June 2027
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

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.

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Other recruiting trials for Histiocytosis

Currently open trials in the same condition.

Other Anna Raciborska trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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