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NCT03672331: MyPeBS
My Personalized Breast Screening
NA trial testing Mammogram in Breast Screening in 53,142 participants. Participants enrolled and being followed up; not accepting new ones.
31 August 2027
Quick facts
| Lead sponsor | UNICANCER |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 53,142 |
| Start date | 18 July 2019 |
| Primary completion | 31 August 2027 |
| Estimated completion | 31 December 2027 |
| Sites | 6 locations across France, Italy, Belgium, United Kingdom, Israel, Spain |
Drugs / interventions tested
- Mammogram
- Ultrasound
- MRI — full drug profile →
- Tomosynthesis
Conditions studied
- Breast Screening — all drugs for Breast Screening →
Sponsor
UNICANCER — full company profile →
Who can join
Adults 40 to 70, female only, with Breast Screening. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
MyPeBS is an international randomized, open-label, multicentric, study assessing the effectiveness of a risk-based breast cancer screening strategy (using clinical risk scores and polymorphisms) compared to standard screening (according to the current national guidelines in each participating country) in detecting stage 2 or higher breast cancers. Women will be differentially screened for 4 years and then, after an end-of-study mammogram, they will return to the routine screening practice. The main study endpoint will be measured at the end of the four years of intervention. Furthermore, follow up data will be collected for 15 years from study entry for evaluation of long-term cumulative breast cancer incidence and breast cancer-specific survival
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
The current status of risk-stratified breast screening.
Clift AK, Dodwell D, Lord S, Petrou S, et al · · 2022 · cited 85× · PMID 34703006 · DOI 10.1038/s41416-021-01550-3 -
Study protocol comparing the ethical, psychological and socio-economic impact of personalised breast cancer screening to that of standard screening in the "My Personal Breast Screening" (MyPeBS) randomised clinical trial.
Roux A, Cholerton R, Sicsic J, Moumjid N, et al · · 2022 · cited 72× · PMID 35524202 · DOI 10.1186/s12885-022-09484-6 -
Cases in Precision Medicine: The Role of Polygenic Risk Scores in Breast Cancer Risk Assessment.
Zeinomar N, Chung WK. · · 2021 · cited 19× · PMID 33253037 · DOI 10.7326/m20-5874 -
Feasibility of personalized screening and prevention recommendations in the general population through breast cancer risk assessment: results from a dedicated risk clinic.
Saghatchian M, Abehsera M, Yamgnane A, Geyl C, et al · · 2022 · cited 13× · PMID 34994879 · DOI 10.1007/s10549-021-06445-8 -
Acceptability of risk-based breast cancer screening among professionals and healthcare providers from 6 countries contributing to the MyPeBS study.
Roux A, Hervouet L, Stefano FD, French DP, et al · · 2025 · cited 5× · PMID 40089664 · DOI 10.1186/s12885-025-13848-z -
Toward Application of Polygenic Risk Scores to Both Enhance and Deintensify Breast Cancer Screening.
Maxwell KN, Domchek SM. · · 2024 · cited 4× · PMID 38422469 · DOI 10.1200/jco.24.00029 -
Evaluating the prognostic performance of a polygenic risk score for breast cancer risk stratification.
Olsen M, Fischer K, Bossuyt PM, Goetghebeur E. · · 2021 · cited 4× · PMID 34930164 · DOI 10.1186/s12885-021-08937-8 -
Insights into genetic modifiers of breast cancer risk in carriers of BRCA1 and BRCA2 pathogenic variants.
Dwornik R, Białkowska K. · · 2025 · cited 1× · PMID 40296163 · DOI 10.1186/s13053-025-00313-y
Verify or expand the search:
- PubMed search for NCT03672331
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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- NCT07277738 — Precision Supplemental Imaging in Women With Dense Breasts · NA · not yet recruiting
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Other recruiting trials for Breast Screening
Currently open trials in the same condition.
- NCT06636539 — Prospective Case Collection Study of Contrast-Enhanced Mammography Imaging Acquired on a New Investigational Device · NA · recruiting
- NCT03233191 — Digital Tomosynthesis Mammography and Digital Mammography in Screening Patients for Breast Cancer · Phase 3 · active not recruiting
Other UNICANCER trials
Trials by the same sponsor.
- NCT07340619 — Clinical Trial Evaluating the Biological Activity of a New Drug Identified as Prifetrastat (PF-07248144), Combined With · Phase 2 · not yet recruiting
- NCT07340567 — Personalizing Chemotherapy Selection After Surgery for Patients With Stage III Colorectal Cancer Using a Blood Test · Phase 3 · not yet recruiting
- NCT07360834 — Study Aiming to Test Whether Non-invasive Liquid Biopsies Can Safely Reduce Invasive Surveillance Methods in Lynch Syndr · NA · not yet recruiting
- NCT07106632 — Optimising Adjuvant Chemotherapy Prescription in Young Patients With Hormone-dependent Breast Cancer Using Genomic Tests · Phase 3 · not yet recruiting
- NCT07294430 — Antibody-based PET Imaging and Treatment Response in Breast Cancer Treated With an Antibody-drug Conjugate. · Phase 2 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03672331 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by UNICANCER
- Last refreshed: 18 September 2025
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/NCT03672331.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing