Pf-06755347 intravenous (DrugBank: -)
1 disease告示番号 | 疾患名(ページ内リンク) | 臨床試験数 |
---|---|---|
63 | 特発性血小板減少性紫斑病 | 1 |
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
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1 | NCT03275740 (ClinicalTrials.gov) | July 17, 2017 | 6/7/2017 | A First in HumanTrial to Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-06755347 | A PHASE 1, RANDOMIZED, DOUBLE-BLIND, SPONSOR-OPEN, PLACEBO-CONTROLLED, FIRST-IN-HUMAN TRIAL TO EVALUATE THE SAFETY, TOLERABILITY, AND PHARMACOKINETICS OF PF-06755347 AFTER SINGLE ASCENDING INTRAVENOUS AND SUBCUTANEOUS DOSING TO HEALTHY ADULT MALE PARTICIPANTS | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating;Primary Immune Thrombocytopenia | Drug: PF-06755347 intravenous;Drug: Placebo intravenous;Drug: PF-06755347 subcutaneous;Drug: Placebo subcutaneous | Pfizer | NULL | Recruiting | 18 Years | 55 Years | Male | 84 | Phase 1 | United States;Belgium;New Zealand;United Kingdom |