Skip to main content

anifrolumab

Generic: anifrolumab·Brand: Saphnelo

anifrolumab: 16 clinical trials tracked.

anifrolumab evidence translation

What we can confirm

16 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about anifrolumab, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence3 indications · 1 study sponsors
Clinical Trial Registry Records (16)showing 10 most recent

A Non-Interventional Descriptive Multi-Country Study of Saphnelo™ (Anifrolumab-fnia) Utilization in Females of Reproductive Potential

NCT07431775Registry updated 2026-02-25·AZN
Not yet recruiting

Primary endpoint: Incidence of anifrolumab use

Observational26,000,000 targetStarted 2026-10Completion 2032-03AstraZeneca

Multicentre, Open-Label, Single-Arm, 52-Week, Ph3b Study to Evaluate the Efficacy and Safety Outcomes in Chinese Patients Treated With Anifrolumab Who Have Active Moderate-Severe Systemic Lupus Erythematosus (SLE)

NCT07751848Registry updated 2026-09-22·Phase 3·AZN
Recruiting

Primary endpoint: The proportion of patients who achieve DORIS remission at week 52

Interventionalopen417 targetStarted 2026-08Completion 2028-0850 sites · ChinaAstraZeneca

ROSY-S: Rollover Study for Participants Who Have Completed a Previous Study With Anifrolumab (Saphnelo) and Are Assessed by the Investigator to Clinically Benefit From Continued Treatment

NCT07691970Registry updated 2026-10-02·Phase 3·AZN
Recruiting

Primary endpoint: SAEs and Non-Serious AEs

Interventionalopen1,072 targetStarted 2026-08Completion 2032-12128 sites · Argentina, Australia, Austria, Belgium…AstraZeneca

A Phase II Open-Label Pilot Trial Assessing the Safety of Anifrolumab in Adult Patients With Primary Antiphospholipid Syndrome (APS). The AnifAPS Trial

NCT07584083Registry updated 2026-06-02·Phase 2
Recruiting

Primary endpoint: Safety and tolerability of anifrolumab

Interventionalopen20 targetStarted 2026-04Completion 2028-061 site · GreeceNational and Kapodistrian University of Athens

Multinational, Interventional, 52-week, Open-label, Single-arm Study to Evaluate the Treatment Outcomes of Anifrolumab 120 mg Subcutaneous Once Weekly in Immunosuppressant-naïve and Biologic-naïve Systemic Lupus Erythematosus (SUNFLOWER)

NCT07430306Registry updated 2026-09-25·Phase 3·AZN
Recruiting

Primary endpoint: Attainment of DORIS remission

Interventionalopen245 targetStarted 2026-04Completion 2029-0150 sites · Canada, France, Germany, United StatesAstraZeneca

A Non-Interventional Multi-Country Post-Authorisation Safety Study (PASS) to Assess the Incidence of Serious Infections & Malignancies in Systemic Lupus Erythematosus (SLE) Patients Exposed to Anifrolumab

NCT07000110Registry updated 2026-09-16·AZN
Recruiting

Primary endpoint: Malignancies

Observational3,506 targetStarted 2026-01Completion 2031-114 sites · Denmark, France, Germany, SpainAstraZeneca

PRIMULA Lac (Prospective Registry Investigating Maternal, Infant, and Lactation Outcomes in Anifrolumab Users): The AstraZeneca Lactation Study for Anifrolumab

NCT06594068Registry updated 2026-09-16·Phase 4·AZN
Recruiting

Primary endpoint: Area under the milk concentration-time curve during a dosing interval

Interventionalopen16 targetStarted 2026-01Completion 2027-081 site · United StatesAstraZeneca

DAHLIA: Achievement of Low Level of Disease Activity With a Dose of Corticosteroids Less Than or Equal to 5 mg (LLDAS5): a Real-life Study With Anifrolumab on Patients With Systemic Lupus Erythematosus in Italy

NCT07330245Registry updated 2026-09-21·AZN
Recruiting

Primary endpoint: Number and percentage of patients achieving LLDAS5

Observational218 targetStarted 2025-12Completion 2028-0922 sites · ItalyAstraZeneca

Pregnancy and Infant Outcomes in Anifrolumab Exposed Pregnancies Using PRegnancy Outcomes Intensive Monitoring (PRIM) Data: The Anifrolumab PRIM Program

NCT06795893Registry updated 2026-09-11·AZN
Recruiting

Primary endpoint: Major congenital malfunctions

Observational240 targetStarted 2025-11Completion 2031-041 site · SwedenAstraZeneca

PRIMULA Preg (Prospective Registry Investigating Maternal and Infant Outcomes in Anifrolumab Users): The AstraZeneca Pregnancy Study for Anifrolumab

NCT06659029Registry updated 2026-06-24·AZN
Recruiting

Primary endpoint: Composite outcome of all major congenital malformations (MCMs)

Observational442 targetStarted 2025-07Completion 2031-041 site · United StatesAstraZeneca