# SMS - Study of Somatic Mutations Using Genome Sequencing

> **NCT06851052** · — · ENROLLING_BY_INVITATION · sponsor: **The Wellcome Sanger Institute** · enrollment: 600 (estimated)

## Conditions studied

- Somatic Mutation

## Interventions

- **OTHER:** sample collection
- **OTHER:** Seeking consent
- **OTHER:** Sample Collection: Surgical

## Key facts

- **NCT ID:** NCT06851052
- **Lead sponsor:** The Wellcome Sanger Institute
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2016-10-01
- **Primary completion:** 2028-06-14
- **Final completion:** 2028-07-14
- **Target enrollment:** 600 (ESTIMATED)
- **Last updated:** 2025-07-20

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06851052

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06851052, "SMS - Study of Somatic Mutations Using Genome Sequencing". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT06851052. Licensed CC0.

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