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Recruiting EARLY_Phase 1 NCT06959979

NCT06959979 Novel Molecular Targets and Innovative Therapeutic Perspective in Medulloblastoma

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Clinical Trial Summary
NCT ID NCT06959979
Status Recruiting
Phase EARLY_Phase 1
Sponsor Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Condition Medulloblastoma, Childhood
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2024-11-25
Primary Completion 2026-08-31

Eligibility & Interventions

Sex All sexes
Min Age 0 Years
Max Age 18 Years
Study Type INTERVENTIONAL
Interventions
CDK4/6 Inhibitor (Palbociclib, Ribociclib, Abemaciclib)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 60 participants in total. It began in 2024-11-25 with a primary completion date of 2026-08-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Medulloblastoma (MB), a rare yet critical pediatric brain tumor, is divided into 4 molecular subgroups (WNT, SHH, Group 3, Group 4), each with distinct genetic profiles. Despite diagnostic and therapeutic advances, neurotoxicity from standard treatments (resection, radiotherapy, chemotherapy) and the need for long-term care remain challenges. CDK4/6 inhibitors (palbociclib, ribociclib, abemaciclib), approved for breast cancer, show potential in other tumors, but their efficacy in MB is unclear. Treatment resistance is a concern. This project aims to identify genetic markers of sensitivity to CDK4/6 inhibitors in MB, to improve therapies and overcome resistance.

Eligibility Criteria

Inclusion Criteria: * All patients affected by Medulloblastoma operated on at the Pediatric Neurosurgery Unit during their pediatric age will be elected to take part to the study

Contact & Investigator

Central Contact

GIANPIERO TAMBURRINI, MD

✉ gianpiero.tamburrini@unicatt.it

📞 3349468776

Frequently Asked Questions

Who can join the NCT06959979 clinical trial?

This trial is open to participants of all sexes, aged 0 Years or older, up to 18 Years, studying Medulloblastoma, Childhood. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06959979 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06959979 currently recruiting?

Yes, NCT06959979 is actively recruiting participants. Contact the research team at gianpiero.tamburrini@unicatt.it for enrollment information.

Where is the NCT06959979 trial being conducted?

This trial is being conducted at Roma, Italy.

Who is sponsoring the NCT06959979 clinical trial?

NCT06959979 is sponsored by Fondazione Policlinico Universitario Agostino Gemelli IRCCS. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology