RecruitingACTRN12609000233224
A Single-Dose Safety and Tolerability Placebo Controlled Study of Subcutaneous SCH 900222 in Healthy Volunteers
Sponsor
Schering-Plough
Enrollment
32 participants
Start Date
Jun 1, 2009
Study Type
Interventional
Conditions
Summary
This study will evaluate the safety, tolerability, & pharmacokinetic response to SCH 900222 subcutaneous fixed dose in healthy subjects.
Eligibility
Sex: Both males and femalesMin Age: 18 YearssMax Age: 45 Yearss
Plain Language Summary
Simplified for easier understanding
This early-stage study is testing the safety and tolerability of a single dose of a new investigational drug called SCH 900222, given by injection under the skin, in healthy volunteers. The aim is to understand how the body handles the drug and to confirm it is safe. This is one of the first tests of this drug in humans.
You may be eligible if:
- You are between 18 and 45 years old (male or female)
- You are in good health
- You have no history of latent or active tuberculosis
You may NOT be eligible if:
- You have a history of cancer, HIV infection, Hepatitis B, or Hepatitis C
- You have active or latent tuberculosis (TB)
Talk to your doctor about whether this trial might be right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
A single dose of either 50mg or 200mg SCH 900222 administered as a subcutaneous single injection.
A single dose of either 50mg or 200mg SCH 900222 administered as a subcutaneous single injection.
Locations(1)
View Full Details on ANZCTR
For the most up-to-date information, visit the official listing.
ACTRN12609000233224