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A phase I/II trial of ABTL0812 in children with relapsed/refractory neuroblastoma and other solid tumours

Status
Withdrawn
Phases
Phase 1Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-504246-64-00
Acronym
ETNA
Enrollment
48
Registered
2023-10-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed/refractory neuroblastoma and other solid tumours

Brief summary

Incidence of dose limiting toxicities assessed during the first cycle of study treatment of ABTL0182 (cohorts A and B).

Interventions

None listed

Sponsors

Fir Huvh Fundacio Institut De Recerca Hospital Universitari Vall De Hebron
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Incidence of dose limiting toxicities assessed during the first cycle of study treatment of ABTL0182 (cohorts A and B).

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026