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ROSY-T: Roll Over StudY for Patients Who Have Completed a Previous Oncology Study with Osimertinib (TAGRISSO) and are Judged by the Investigator to Clinically Benefit From Continued Treatment

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-501528-58-00
Acronym
D5161N00007
Enrollment
2
Registered
2023-08-09
Start date
2023-10-16
Completion date
Unknown
Last updated
2025-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Various tumor types depending on the parent study

Brief summary

SAEs and serious AESIs reported until 28 days after the last dose of study treatment

Interventions

DRUGTAGRISSO 80 mg film-coated tablets
DRUGTAGRISSO 40 mg film-coated tablets

Sponsors

Astrazeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
SAEs and serious AESIs reported until 28 days after the last dose of study treatment

Countries

France, Poland

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026