Study of ASKP1240 After a Single Intravenous Dose at Escalating Dose Levels in Healthy Subjects

Astellas

Status and phase: Completed; Phase 1

Conditions: Healthy Volunteers; Pharmacokinetics of ASKP1240

Treatments: Drug: Placebo; Drug: ASP1240

Study type: Interventional

Funder types: Industry

Identifiers

NCT01565681

7163-CL-0101

Details and patient eligibility

About

The objective of this study is to evaluate the safety, tolerability, pharmacodynamics and pharmacokinetics of ASKP1240 after a single intravenous dose at escalating dose levels in healthy subjects.

Enrollment: 109 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• The subject weighs at least 50 kg, and has a body mass index (BMI) of 18 to 32 kg/m2 inclusive
• The female subject must be of non-childbearing potential (surgically sterile [hysterectomy or bilateral tubal ligation] or post-menopausal ≥ 1 year with follicle stimulating hormone [FSH] > 40 U/L)
• Male subject agrees to no sperm donation until end of study or 90 days post dose, whichever is longer
• The subject is highly likely to comply with the protocol and complete the study
• The subject has a negative urine screen for drugs of abuse, and negative blood or breathalyzer alcohol screen at Screening and clinic admission on Day 1

Exclusion criteria

• The subject has a history of severe allergic or anaphylactic reactions

• The subject has history of consuming more than 14 units of alcoholic beverages per week or has a history of alcoholism or drug/chemical/substance abuse within past 2 years prior to screening (Note: one unit = 12 ounces of beer, 4 ounces of wine or 1 ounce of spirits)

• The subject has/had a symptomatic, viral, bacterial (including upper respiratory infection), or fungal (non-cutaneous) infection within 1 week prior to clinic check in

• The subject has a supine mean systolic blood pressure < 90 or > 160 mmHg and a mean diastolic blood pressure < 50 or > 90 mmHg, or pulse rate higher than 100 beats per min (bpm), either at screening or clinic check in (blood pressure measurements taken in triplicate after subject has been resting in a supine position for a minimum of 5 minutes)

• The subject is known positive for human immunodeficiency virus (HIV) antibody

• The subject has a positive test for hepatitis C antibody, or for hepatitis B virus surface antigen (HBsAg)

• The subject has at screening or clinic check in that:

  1. white blood cell count (WBC) is < 3.5 or > upper limit of normal
  2. absolute neutrophil count (ANC) is <1.5 or > upper limit of normal
  3. platelet count (PLT) is outside the normal limit
  4. serum creatinine, total bilirubin, alanine aminotransferase (ALT), or aspartate aminotransferase (AST) are > upper limit of normal
  5. creatine phosphokinase (CPK) is > two times upper limit of normal
  6. international normalized ratio (INR) is > upper limit of normal
  7. OR remaining laboratory tests are outside the normal limits and considered by the investigator to be clinically significant with regard to the remaining per protocol laboratory tests

• The subject has received a vaccine within 60 days prior to study drug administration

• The subject has received any systemic immunosuppressant agent within 6 months prior to study drug administration.

• The subject has received any antibody or biologic product within 6 months prior to study drug administration

• The subject has received any systemic steroid within 2 months prior to study drug administration

• The subject has had treatment with prescription or non-prescription drugs, including complementary and alternative medicines (CAM) and excluding over-the-counter (OTC) allergy medications, nasal steroids, nasal inhalers, oral contraceptives, stable hormone replacement therapy (HRT; per Investigator judgment and dose change not expected during study), and intermittent acetaminophen, within 14 days prior to study drug administration

• The subject has received an experimental agent within 30 days or ten half-lives, whichever is longer, prior to study drug administration

• The subject is participating in another clinical trial or has participated in another dose group of the current trial

• The subject has donated or has had significant blood loss or received a transfusion of any blood or blood products within 60 days or donated plasma within 7 days prior to dosing

• The subject has a history of heavy smoking or has used tobacco-containing products and nicotine or nicotine-containing products in the past six months prior to Screening

• The subject has a history of thromboembolic or vascular disease especially deep vein thrombosis, pulmonary embolism and varices

• The subject has a positive test for tuberculosis

Trial design

109 participants in 13 patient groups, including a placebo group

Arm A: ASKP1240 lowest dose

Experimental group

Treatment:

Drug: ASP1240

Arm B: ASKP1240 second lowest dose

Experimental group

Treatment:

Drug: ASP1240

Arm C: ASKP1240 third lowest dose

Experimental group

Treatment:

Drug: ASP1240

Arm D: ASKP1240 fourth lowest dose

Experimental group

Treatment:

Drug: ASP1240

Arm E: ASKP1240 fifth lowest dose

Experimental group

Treatment:

Drug: ASP1240

Arm F: ASKP1240 middle dose

Experimental group

Treatment:

Drug: ASP1240

Arm G: ASKP1240 sixth highest dose

Experimental group

Treatment:

Drug: ASP1240

Arm H: ASKP1240 fifth highest dose

Experimental group

Treatment:

Drug: ASP1240

Arm I: ASKP1240 fourth highest dose

Experimental group

Treatment:

Drug: ASP1240

Arm J: ASKP1240 third highest dose

Experimental group

Treatment:

Drug: ASP1240

Arm K: ASKP1240 second highest dose

Experimental group

Treatment:

Drug: ASP1240

Arm L: ASKP1240 highest dose

Experimental group

Treatment:

Drug: ASP1240

Arm M: Placebo

Placebo Comparator group

Description:

Sodium Chloride solution

Treatment:

Drug: Placebo