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NCT03524430: BREVITY
RNA Disruption Assay (RDA)-Breast Cancer Response Evaluation for Individualized Therapy
NA trial testing Core needle biopsy in Breast Neoplasm Female in 801 participants. Currently enrolling.
30 July 2026
Quick facts
| Lead sponsor | Rna Diagnostics Inc. |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 801 |
| Start date | 26 April 2018 |
| Primary completion | 30 July 2026 |
| Estimated completion | 31 March 2031 |
| Sites | 7 locations across France, Italy, Germany, Poland, Canada, United States, Spain |
Drugs / interventions tested
- Core needle biopsy
Conditions studied
- Breast Neoplasm Female — all drugs for Breast Neoplasm Female →
Sponsor
Rna Diagnostics Inc.
Who can join
18 and older, female only, with Breast Neoplasm Female. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The current study aims to provide validation results of RNA Disruption Assay (RDA) as a tumour response assessment tool that uses tumour core biopsies taken starting from 35 +/- 4 days after the initiation of neoadjuvant chemotherapy.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
RNA modifications in cancer.
Wu H, Chen S, Li X, Li Y, et al · · 2025 · cited 5× · PMID 39802639 · DOI 10.1002/mco2.70042 -
High mid-treatment tumour RNA disruption in patients with HER2-negative breast cancer is associated with improved disease-free survival after neoadjuvant chemotherapy.
Parissenti AM, Pritzker LB, Dahle MA, Gythfeldt HVL, et al · · 2025 · cited 2× · PMID 40790765 · DOI 10.1186/s13058-025-02092-9 -
Low RNA disruption during neoadjuvant chemotherapy predicts pathologic complete response absence in patients with breast cancer.
Cazzaniga ME, Ademuyiwa F, Petit T, Tio J, et al · · 2024 · cited 2× · PMID 38113421 · DOI 10.1093/jncics/pkad107 -
Ribosomal RNA Degradation (RNA Disruption) in Tumour Cells: Mechanistic Insights and Potential Clinical Utility.
Parissenti AM, Noubir S, Pritzker LB, Kovala T, et al · · 2025 · PMID 40940865 · DOI 10.3390/cancers17172769
Verify or expand the search:
- PubMed search for NCT03524430
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other recruiting trials for Breast Neoplasm Female
Currently open trials in the same condition.
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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 NCT03524430 (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 Rna Diagnostics Inc.
- Last refreshed: 14 October 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/NCT03524430.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing