ClinicalTrials.Veeva

Menu

Adverse Effects of ATG/ALG Therapy in Aplastic Anemia

I

Institute of Hematology & Blood Diseases Hospital, China

Status

Enrolling

Conditions

Aplastic Anaemia

Treatments

Drug: ATG/ALG

Study type

Observational

Funder types

Other

Identifiers

NCT07461116
AA-ATG/ALG-20260108

Details and patient eligibility

About

This prospective, single-center, observational cohort study aims to systematically observe and describe the clinical characteristics of adverse reactions in patients with aplastic anemia undergoing ATG (Anti-Thymocyte Globulin) /ALG (Anti-Lymphocyte Globulin) treatment, providing a data foundation for the development of relevant management strategies. This study plans to enroll 200 aplastic anemia patients undergoing ATG/ALG treatment

Enrollment

200 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meet the diagnostic criteria for aplastic anemia (Camitta criteria);
  • Receiving ATG/ALG immunosuppressive therapy for the first time;

Exclusion criteria

  • Previously received hematopoietic stem cell transplantation;
  • Aplastic anemia patients receiving ATG/ALG as part of transplant conditioning regimen;

Trial design

200 participants in 1 patient group

Patients with aplastic anemia undergoing ATG or ALG treatment
Treatment:
Drug: ATG/ALG

Trial contacts and locations

1

Loading...

Central trial contact

Weiwang Li, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems