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Recruiting NCT06725173

NCT06725173 Detailed Phenotypic and Genotype Study to Correlate RB1 Mutations Relating to Primary Ocular Tumors and Secondary Extra-ocular Metastasis.

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Clinical Trial Summary
NCT ID NCT06725173
Status Recruiting
Phase
Sponsor University of Washington
Condition Retinoblastoma Bilateral
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2026-03-16
Primary Completion 2030-01-01

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Targeted Long-read sequencing

Eligibility Fast-Check

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

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2026-03-16 with a primary completion date of 2030-01-01.

⚠ 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

The goal of this observational study is undertake a detailed phenotypic and genotypic study of patients with ocular and secondary cancers due to mutations in the RB1 gene. Our research sequencing approach will allow advanced insight to for further detailed genotypic understanding of parent-of-origin for valuable insight into the genotype-phenotype relationship of this cancer syndrome.

Eligibility Criteria

Inclusion Criteria: * Patients with molecularly proven retinoblastoma due to RB1 or a typical clinical retinoblastoma phenotype with genetic screening pending. * Able to give consent/parent or guardian able to give consent. Exclusion Criteria: * Patients unable or unwilling to undertake consent or clinical testing. * Patients unwilling to donate a saliva or blood sample in order to establish the genetic cause of their condition.

Contact & Investigator

Central Contact

Debarshi Mustafi, MD PhD

✉ debarshi@uw.edu

📞 206-683-6305

Principal Investigator

Debarshi Mustafi, MD PhD

PRINCIPAL INVESTIGATOR

University of Washington

Frequently Asked Questions

Who can join the NCT06725173 clinical trial?

This trial is open to participants of all sexes, studying Retinoblastoma Bilateral. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06725173 currently recruiting?

Yes, NCT06725173 is actively recruiting participants. Contact the research team at debarshi@uw.edu for enrollment information.

Where is the NCT06725173 trial being conducted?

This trial is being conducted at Seattle, United States.

Who is sponsoring the NCT06725173 clinical trial?

NCT06725173 is sponsored by University of Washington. The principal investigator is Debarshi Mustafi, MD PhD at University of Washington. The trial plans to enroll 100 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: April 2026  ·  Data Methodology