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NCT06255210: ESICON

Efficacy and Safety of Induction Chemotherapy for Olfactory Neuroblastoma (ESICON)

Recruiting now Phase 2 Last updated 13 February 2024
What this trial tests

Phase 2 trial testing Gemcitabine+Cisplatin(GP); Cyclophosphamide+Etoposide+Cisplatin(CEP) in Olfactory Neuroblastoma in 25 participants. Currently enrolling.

Timeline
1 March 2024
Primary endpoint
1 March 2027
1 March 2030

Quick facts

Lead sponsorHongmeng Yu
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment25
Start date1 March 2024
Primary completion1 March 2027
Estimated completion1 March 2030
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Hongmeng Yu — full company profile →

Who can join

18 and older, any sex, with Olfactory Neuroblastoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to learn about the induction chemotherapy efficacy in olfactory neuroblastoma. The main question it aims to answer is: wether olfactory neuroblastoma patients with different pathology subtypes apply to different induction chemotherapy schemes. Participants will be treated with different chemotherapy schemes, to evaluate the tumor remission rate and long term survival.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Olfactory Neuroblastoma

Currently open trials in the same condition.

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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/NCT06255210.

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