Lupus Trial, Recruiting NCT06659029 Sponsor: AstraZeneca Condition: Lupus
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Lupus Trial, Recruiting

NCT06659029
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

Group 1 (Exposed group – for people who have taken anifrolumab):

  • You are currently pregnant or were pregnant within the last year
  • You have been diagnosed with moderate or severe lupus (SLE)
  • You are willing to give your consent to take part in the study
  • You agree to allow your doctor(s) to share your health information with the registry
  • You have received at least one dose of the medication anifrolumab at any point during your pregnancy

Group 2 (Unexposed group – for people who have NOT taken anifrolumab):

  • You are currently pregnant or were recently pregnant
  • You have been diagnosed with moderate or severe lupus (SLE)
  • You are willing to give your consent to take part in the study
  • You agree to allow your doctor(s) to share your health information with the registry
  • You are taking or have taken other medications to treat your moderate or severe lupus during pregnancy

Who may not be able to join:

Group 1 (Exposed group):

  • Your pregnancy has already ended before you first made contact with the study team to enroll
  • You were exposed during pregnancy to medications known to cause birth defects, or to experimental/investigational medications

Group 2 (Unexposed group):

  • Your pregnancy has already ended before you first made contact with the study team to enroll
  • You were exposed during pregnancy to medications known to cause birth defects, or to experimental/investigational medications

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 1-877-240-9479

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
1 July 2025
Est. completion
15 April 2031

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Composite outcome of all major congenital malformations (MCMs)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov