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ALPHA-1 ANTITRYPSIN DEFICIENCY

Alpha-1 Antitrypsin Deficiency Recruitment

Specialized recruitment for AATD and related lung disease trials with comprehensive pulmonary expertise.

180+
AATD Patients Successfully Recruited
7+
Completed Alpha-1 Studies
68%
Faster Enrollment Than Industry Average
96%
Patient Retention Rate in AATD Trials

Alpha-1 Antitrypsin Deficiency Specializations

Comprehensive recruitment strategies for all phenotypes and manifestations of AATD.

Severe AATD (ZZ Phenotype)

Most severe deficiency requiring aggressive treatment

  • Augmentation therapy trials
  • Lung transplant studies
  • Gene therapy research

Moderate AATD (SZ Phenotype)

Intermediate deficiency with variable symptoms

  • Progression monitoring
  • Prevention studies
  • Quality of life assessments

AATD-Related Emphysema

Lung damage from alpha-1 antitrypsin deficiency

  • Bronchodilator studies
  • Anti-inflammatory trials
  • Surgical interventions

AATD Liver Disease

Hepatic manifestations of alpha-1 deficiency

  • Hepatoprotective studies
  • Liver function monitoring
  • Transplant protocols

Pediatric AATD

Children with early-onset alpha-1 deficiency

  • Growth monitoring
  • Early intervention
  • Family screening studies

Augmentation Therapy

Patients receiving or eligible for replacement therapy

  • Dosing optimization
  • Efficacy studies
  • Long-term safety monitoring

Ready to Accelerate Your AATD Clinical Trial?

Partner with our expert team to access our specialized network of alpha-1 antitrypsin deficiency patients.