A clinical trial is any investigation in human subjects intended to discover or verify the safety and efficacy of the product.
Anybody can participate in the clinical trial. Each clinical trial defines who is eligible to take part in the study. If you are eligible your Physician will approach and explain further on the clinical trial schedule.
All of the records and data from your participation will be kept confidential. The results of your participation in this study may be used for publication or for scientific purposes, but neither your name nor your identity will be disclosed unless you give separate  specific consent to this, or unless required by law. The research records for this study may be reviewed by some agencies.
There are both benefits and risks associated with clinical trials.
Reimbursed based on the subjects’ anticipated expenses incurred during participation in a study (e.g., parking, meals, travel).
There is no direct compensation if you are participate in the study, however if you experienced any side effect or serious side effect direct from the investigational product which need further treatment there is insurance coverage secured by the sponsor provided you are comply with the instruction given.
Your participation is strictly voluntary. Refusal to participate will not involve any penalty, loss of benefits, or reduction in the quality of medical care.
You are free to withdraw at any time for any reason, this will not affect in any way the quality of health care you will receive.
For more information regarding your rights as a research patient, you may contact IJN Research Ethics Committee (IJNREC) at 03 2617 8266/8264
For more information regarding clinical trials, you may contact the physician who enrolled you in the study at 03 2617 8200