Phase 3 Myasthenia Gravis Trial, Recruiting NCT06607627 Sponsor: Alexion Pharmaceuticals, Inc. Condition: Myasthenia Gravis
Back to Myasthenia Gravis

Phase 3 Myasthenia Gravis Trial, Recruiting

NCT06607627
Recruiting Phase 3

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:

  • (USA only) You must be between 12 and 17 years old at the time of signing the consent form
  • (Outside USA) You must be between 6 and 17 years old at the time of signing the consent form
  • (USA only) You must have received a meningococcal vaccine covering strains A, B, C, W, and Y within the last 3 years, and at least 2 weeks before starting the study
  • (Outside USA) You must have received a meningococcal vaccine covering strains A, C, W, and Y (and B if available in your country) within the last 3 years before starting the study — if the vaccine was given less than 2 weeks before starting, you would need to take preventive antibiotics for at least 2 weeks
  • You must have been diagnosed with Myasthenia Gravis (MG) — a condition causing muscle weakness — that falls into a moderate or more severe category as defined by a recognised medical classification system (confirm with trial site)
  • You must have a positive blood test showing specific antibodies linked to MG (called AChR antibodies)

Who may not be able to join:

  • People who have had their thymus gland removed or had any other thymus surgery within the past 12 months
  • People who have an untreated cancerous or abnormal growth on the thymus gland
  • People who have previously had a serious bacterial infection called meningococcal disease
  • People who are pregnant, breastfeeding, or planning to become pregnant during the study

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 28 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 1-855-752-2356

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
Phase 3
Sponsor
Alexion Pharmaceuticals, Inc.
Registry
ClinicalTrials.gov
Start date
13 November 2024
Est. completion
15 December 2026

Where this trial is recruiting

🇧🇷 Brazil 🇯🇵 Japan 🇵🇱 Poland 🇹🇼 Taiwan 🇺🇸 United States

Primary endpoints

Maximum Observed Serum Concentration (Cmax) of Gefurulimab; Serum Free Complement Component 5 (C5) Concentration

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: 28 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