RECRUITING Phase 3 ClinicalTrials.gov

Rollover Study for Participants Who Have Completed a Previous Clinical Study With Anifrolumab (Saphnelo) and Clinically Benefited From Continued Treatment

Sponsor: AstraZeneca • ClinicalTrials.gov ID: NCT07691970

Registry updated: 2026-10-02

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Description

The purpose of this study is to provide continued access to anifrolumab to eligible participants who are continuing to derive clinical benefit from treatment at the end of a parent clinical study, as assessed by the Investigator, while monitoring safety and tolerability. Study details include: * Participants can transition in ROSY-S once they complete their participation in the parent study and should have received at least one dose of anifrolumab in the parent study. Participants with a treatment gap from parent studies and/or who are on compassionate use are eligible to rollover to ROSY-S study. * The earliest that the Enrolment Visit may occur is at the time of the last visit of the parent study (ie, completion of the parent study's final safety follow-up visit). All required assessments from the safety follow-up visit of the parent study must be completed before the Enrolment Visit of ROSY-S study. * The participants will continue to receive anifrolumab the same way they received it in the parent trial * A participant is considered to have completed the study when they meet one of the discontinuation criteria. * Safety will be monitored throughout the study. Both serious and nonserious AEs will be collected up to 12 weeks after the last dose of anifrolumab and will be reported as part of the primary safety endpoint.

Interventions

Anifrolumab (Combination product)
Anifrolumab pre-filled syringe
Anifrolumab (Combination product)
Anifrolumab solution for injection in pre-filled pen
Anifrolumab (Drug)
Anifrolumab concentrate for solution for infusion

Eligibility criteria

Inclusion Criteria: * Participants are eligible to be included in the study only if all of the following criteria apply: 1 Participants must have completed the entirety of the parent study and should have received at least one dose of anifrolumab in the parent study. * In the opinion of the Investigator, the potential benefit to the participant of continuing anifrolumab at the end of the parent study outweighs the risk. * Contraceptive use by participants should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. Participants should continue following the contraception requirements as per Appendix B from study enrolment up to 16 weeks after the last dose of study treatment. * Capable of giving signed informed consent described in Appendix A which includes compliance with the requirements and restrictions listed in the ICF and in this protocol. * Capable of adhering to the treatment plan related to this ROSY-S study. Exclusion Criteria: * Participant develops hypersensitivity to any of the components of anifrolumab. * Female participant who is breastfeeding, pregnant, or intends to become pregnant during participation in this study. * Currently participating in any investigational study or participated in an investigational study within 30 days prior to enrolment or within 5 half-lives of the investigational medicinal product (other than the parent study for anifrolumab) whichever is longer. * Ongoing, unresolved AE requiring interruption of treatment at the end of the prior parent study (ie, when the parent study is either completed or closed) that in the Investigator's opinion would prevent restarting anifrolumab. * Currently receiving or have received prohibited medication(s) as specified in parent protocols prior to signing ICF. * Participants who are planning to use live/live-attenuated vaccines. * Participants who are planning to use any other therapies, including B-cell therapies, that in the opinion of the Investigator could jeopardize or would compromise the participant's ability to participate in the program as determined by the Investigator. * Participants with any medical condition (such as cancer or viral infections \[hepatitis\]) or psychiatric condition that, in the opinion of the Investigator, could jeopardise or would compromise the participant's ability to participate in this study as determined by the Investigator based on protocol required assessments. * Participants who discontinued the parent study prior to completion of all study visits. * Local access to approved and commercially available (reimbursed) drug for the defined indication as permitted by local/country regulation.

Conditions

Systemic Sclerosis Cutaneous Lupus E Myopathies Systemic Lupus Erythematosus

Locations

Research Site — Phoenix, Arizona, United States
Research Site — Los Angeles, California, United States
Research Site — San Francisco, California, United States
Research Site — Boca Raton, Florida, United States
Research Site — Fort Lauderdale, Florida, United States
Research Site — Chicago, Illinois, United States
Research Site — Ann Arbor, Michigan, United States
Research Site — Rochester, Minnesota, United States
Research Site — Omaha, Nebraska, United States
Research Site — New York, New York, United States
Research Site — Charlotte, North Carolina, United States
Research Site — Cleveland, Ohio, United States
Research Site — Portland, Oregon, United States
Research Site — Charleston, South Carolina, United States
Research Site — Roanoke, Virginia, United States
Research Site — Quilmes, Argentina
Research Site — San Miguel, Argentina
Research Site — Melbourne, Australia
Research Site — Mitcham, Australia
Research Site — Graz, Austria
Research Site — Graz, Austria
Research Site — Linz, Austria
Research Site — Vienna, Austria
Research Site — Ghent, Belgium
Research Site — Rio de Janeiro, Brazil
Research Site — Salvador, Brazil
Research Site — Santa Efigênia, Brazil
Research Site — São Paulo, Brazil
Research Site — Plovdiv, Bulgaria
Research Site — Sofia, Bulgaria
Research Site — Sofia, Bulgaria
Research Site — Québec, Canada
Research Site — Santiago, Chile
Research Site — Beijing, China
Research Site — Chongqing, China
Research Site — Guangzhou, China
Research Site — Jinan, China
Research Site — Lanzhou, China
Research Site — Shanghai, China
Research Site — Shenzhen, China
Research Site — Shenzhen, China
Research Site — Bogotá, Colombia
Research Site — Prague, Czechia
Research Site — Bordeaux, France
Research Site — Paris, France
Research Site — Paris, France
Research Site — Strasbourg, France
Research Site — Toulouse, France
Research Site — Dresden, Germany
Research Site — Essen, Germany
Research Site — Kiel, Germany
Research Site — Mainz, Germany
Research Site — Marburg, Germany
Research Site — Tübingen, Germany
Research Site — Chaïdári, Greece
Research Site — Hyderabad, India
Research Site — Kolkata, India
Research Site — New Delhi, India
Research Site — Pune, India
Research Site — Haifa, Israel
Research Site — Kfar Saba, Israel
Research Site — Brescia, Italy
Research Site — Cona, Italy
Research Site — Florence, Italy
Research Site — Milan, Italy
Research Site — Milan, Italy
Research Site — Roma, Italy
Research Site — Roma, Italy
Research Site — Kanazawa, Japan
Research Site — Maebashi, Japan
Research Site — Nagoya, Japan
Research Site — Sapporo, Japan
Research Site — Yokohama, Japan
Research Site — Guadalajara, Mexico
Research Site — Guadalajara, Mexico
Research Site — San Luis Potosí City, Mexico
Research Site — Rotterdam, Netherlands
Research Site — Iloilo City, Philippines
Research Site — Lipa City, Philippines
Research Site — Manila, Philippines
Research Site — Bydgoszcz, Poland
Research Site — Katowice, Poland
Research Site — Kielce, Poland
Research Site — Krakow, Poland
Research Site — Ossy, Poland
Research Site — Warsaw, Poland
Research Site — Braga, Portugal
Research Site — Lisbon, Portugal
Research Site — Porto, Portugal
Research Site — Bucharest, Romania
Research Site — Cluj-Napoca, Romania
Research Site — Iași, Romania
Research Site — Belgrade, Serbia
Research Site — Kragujevac, Serbia
Research Site — Košice, Slovakia
Research Site — Piešťany, Slovakia
Research Site — Johannesburg, South Africa
Research Site — Seoul, South Korea
Research Site — Seoul, South Korea
Research Site — Seoul, South Korea
Research Site — Seoul, South Korea
Research Site — Barcelona, Spain
Research Site — Barcelona, Spain
Research Site — Castellon, Spain
Research Site — Granada, Spain
Research Site — Las Palmas de Gran Canaria, Spain
Research Site — Madrid, Spain
Research Site — Madrid, Spain
Research Site — Valencia, Spain
Research Site — Valencia, Spain
Research Site — Vigo, Spain
Research Site — Kaohsiung City, Taiwan
Research Site — Kaohsiung City, Taiwan
Research Site — Taichung, Taiwan
Research Site — Taipei, Taiwan
Research Site — Bangkok, Thailand
Research Site — Bangkok, Thailand
Research Site — Hat Yai, Thailand
Research Site — Khon Kaen, Thailand
Research Site — Klong Luang, Thailand
Research Site — Fatih-Istanbul, Turkey (Türkiye)
Research Site — Cambridge, United Kingdom
Research Site — Leeds, United Kingdom
Research Site — London, United Kingdom
Research Site — London, United Kingdom
Research Site — Newcastle upon Tyne, United Kingdom
Research Site — Sheffield, United Kingdom
Research Site — Hà Nội, Vietnam

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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

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