Clinical trial

A Randomized, Double-blind, Placebo-controlled, Phase II Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of ARGX-113 in Patients With Primary Immune Thrombocytopenia

Name
ARGX-113-1603
Description
The purpose of the study is to determine safety, efficacy, tolerability and Pharmacokinetics of ARGX-113 in Patients with Primary Immune Thrombocytopenia.
Trial arms
Trial start
2017-03-13
Estimated PCD
2019-04-09
Trial end
2019-04-09
Status
Completed
Phase
Early phase I
Treatment
ARGX-113
ARGX-113 (Dose A or Dose B) or matching placebo will be administered IV weekly
Arms:
ARGX-113 Dose A + SoC, ARGX-113 Dose B +SoC
Placebo
ARGX-113 (Dose A or Dose B) or matching placebo will be administered IV weekly
Arms:
Placebo + SoC
Size
38
Primary endpoint
Incidence and severity of serious adverse events (SAEs).
After the first administration of Investigational Medicinal Product day 1 to 30 days of a patient's last visit.
Eligibility criteria
Inclusion Criteria: 1. Male or female patients aged ≥ 18 to ≤ 85 years. 2. Must receive SoC treatment for ITP that has been stable in dose and frequency for at least 4 weeks prior to Screening. SoC may include oral corticosteroids and/or permitted oral immunosuppressants and/or TPO-R agonist. 3. Confirmed diagnosis of ITP with blood platelet counts \< 30 × 109/L and who have not experienced major bleeding in the last 4 weeks prior to Screening. Exclusion Criteria: 1. Use of anticoagulants, or any drug with antiplatelet effect within 3 weeks prior to Screening. 2. Patients who have received any blood support or transfusion within 4 weeks prior to Screening. 3. Use of Intravenous immunoglobulin G (IVIg) or anti-D immunoglobulin treatment within 4 weeks prior to screening. 4. Use of recombinant thrombopoietin at any time. 5. Use of rituximab within 6 months prior to Screening. Use of any anti-CD20 other than rituximab at any time is not permitted. 6. Use of immunosuppressants is not permitted within 4 weeks prior to Screening, with the exception of the following oral immunosuppressants: azathioprine, danazol, mycophenolate mofetil, mycophenolate sodium which must have been stable for at least 4 weeks prior to Screening. 7. Use of any other biological therapy or investigational drug than those previously indicated within 3 months or 5 half-lives of the drug (whichever is longer) prior to Screening. 8. Received vaccinations within 4 weeks prior to Screening or planned during the study. 9. At Screening, have clinically significant laboratory abnormalities 10. History of any thrombotic or embolic event within 12 months prior to Screening. 11. Known auto-immune disease other than ITP.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Protocol designed to evaluate one or more interventions for treating a disease, syndrome or condition.', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 38, 'type': 'ACTUAL'}}
Updated at
2023-07-25

1 organization

1 product

1 indication

Organization
Argenx
Product
ARGX-113