Continued durvalumab treatment for patients from earlier cancer studies
Gives durvalumab to cancer patients who finished an earlier durvalumab study and still benefit.
Plain-language title generated from the registry record
Registry title: Roll Over StudY for Patients Who Have Completed a Previous Oncology Study with Durvalumab
Key facts
- Where
- Barcelona, Girona, Madrid, Marbella, Santiago De Compostela, and Valencia, SpainSee the 7 sites
- Phase
- Phase 3
Where in Spain
- Hospital de la Santa Creu i Sant PauBarcelona, SpainTaking people
- Hospital Universitari Vall d'HebronBarcelona, SpainTaking people
- Hospital Universitari de Girona Doctor Josep TruetaGirona, SpainTaking people
- Hospital Universitario La PazMadrid, SpainTaking people
- Hospital Costa del SolMarbella, SpainTaking people
- Fundacion Instituto De Investigacion Sanitaria De Santiago De CompostelaSantiago De Compostela, SpainTaking people
- Hospital Universitario Y Politecnico La FeValencia, SpainTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Astrazeneca AB
- Trial code
- NCT05303532EU 2023-507337-22-00
- Record updated
- 8 September 2026
- Original description
To provide continuous study treatment to patients who continue to benefit at the end of a clinical study, while monitoring safety and tolerability.Read full original descriptionShow less
Roll Over Study for Patients Who Have Completed a Previous Oncology Study with Durvalumab and Are Judged by the Investigator to Clinically Benefit From Continued Treatment
To provide continuous study treatment to patients who continue to benefit at the end of a clinical study, while monitoring safety and tolerability.
Inclusion: Provision of signed and dated, written ICF; Patient is currently deriving clinical benefit, as judged by the Investigator, from continued treatment in an AZ parent study using an AZ compound that has met its endpoints, or has otherwise stopped, or the patient has reached maximum treatment duration allowed in the parent study's protocol; Patient can receive durvalumab as a fixed dose of 1500 mg Q4W at study entry.
Exclusion: Core Protocol exclusion criteria: Currently receiving treatment with any prohibited medication(s); Core Protocol exclusion criteria: Local access to commercially-available drug at no cost to the patient as permitted by local/country regulation; Additional exclusion criteria for the ROSY-D sub-study: Ongoing, unresolved, Grade 2 toxicity with an inability to reduce corticosteroid to a dose of ≤ 10 mg of prednisone per day (or equivalent) within 12 weeks after last dose of study treatment/study regimen, as per Toxicity Dose Modification and TMGs for Immune-mediated, Infusion-related, and Non-Immune-mediated Reactions Guidelines of the parent study; Core Protocol exclusion criteria: Permanent discontinuation from the parent study due to toxicity or disease progression (increase in the severity of the disease under study and/or increases in the symptoms of a patient’s condition attributable to the disease, as assessed and documented by the Investigator. Physician-defined progression can be radiological [eg, Response Evaluation Criteria in Solid Tumours] progression or clinical progression); Additional exclusion criteria for the ROSY-D sub-study: Active infection including COVID-19 (PCR confirmed and/or clinically suspected), tuberculosis, hepatitis B (known positive HBsAg result), hepatitis C, or HIV (positive HIV 1/2 antibodies); Core Protocol exclusion criteria: Ongoing, unresolved, Grade 3 or above toxicity requiring interruption of treatment at the time of the termination of the parent study; Core Protocol exclusion criteria: Concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study; Additional exclusion criteria for the ROSY-D sub-study: Male or female patients of reproductive potential who are not willing to employ effective birth control from study inclusion up to 90 days after the last dose of durvalumab monotherapy.