Phase 3 Study to Evaluate the Efficacy & Safety of Self-Administered Injections of BMN165 by Adults With PKU

INCLUSION CRITERIA

Individuals eligible to participate in this study must meet all of the following criteria:

Have completed a prior BMN 165 study (PAL-003, 165-205, or 165-301) prior to screening
Have had a stable BMN 165 dose regimen for at least 14 days prior to screening

Are at least 18 y/o and no older than 70 y/o at screening

Subjects who are < 18 y/o and are already enrolled into Study 165-301 under Amendment #1 (10JAN2014) may enroll into this study
Has identified a person who is > 18 y/o who has the neurocognitive and linguistic capacities to comprehend and complete the Profile of Mood States (POMS)-Observer rated scale

Has identified a competent person(s) > 18 y/o who can observe the subject during study drug administration at certain points in the study

A home healthcare nurse may perform the study drug observations
Are willing and able to provide written, signed informed consent after the nature of the study has been explained and prior to any research-related procedures; for minors, parent or guardian provides written consent and assent may be requested
Are willing and able to comply with all study procedures
For females of childbearing potential, a negative pregnancy test at screening and willing to have additional pregnancy tests during the study

If sexually active, willing to use two acceptable methods of contraception during and for 4 weeks after the study

Males post vasectomy for 2 years with no known pregnancies do not need to use any other forms of contraception during the study.
Females who have been in menopause for at least 2 years, have had a tubal ligation at least 1 year prior to screening, or have had a total hysterectomy do not need to use any other forms of contraception during the study.
Have received documented approval from a study dietitian confirming that the subject is capable of maintaining their diet
Have neurocognitive and linguistic capacities to comprehend and answer investigator's prompts for the Attention Deficit Hyperactivity Disorder Rating Scale (ADHD-RS) Investigator rated instrument and to complete the POMS-Subject rated scale
If applicable, maintained stable dose of medication for Attention Deficit Hyperactivity Disorder (ADHD), depression, anxiety, or other psychiatric disorder ≥8 weeks prior to enrollment and willing to maintain stable dose throughout study unless a change is medically indicated
General good health, as evidenced by physical examination, clinical laboratory evaluations, and ECG tests at screening

Exclusion Criteria

Individuals who meet any of the following exclusion criteria will not be eligible to participate in the study:

Use of any investigational product (except BMN 165) or investigational medical device within 30 days prior to screening or requirement for any investigational agent prior to completion of all scheduled study assessments
Use of any medication (except BMN 165) intended to treat PKU, including the use of large neutral amino acids, within 2 days prior to the administration of study drug
Have known hypersensitivity to Dextran® or components of Dextran
Use or planned use of any injectable drugs containing PEG (except for BMN 165), including medroxyprogesterone injection, within 3 months prior to screening and during study participation
Current use of levodopa
A positive test for HIV antibody, hepatitis B surface antigen, or hepatitis C antibody
A history of organ transplantation or taking chronic immunosuppressive therapy
A history of substance abuse in the past 12 months or current alcohol or drug abuse
Current participation in the Kuvan registry study (PKUDOS). Patients may discontinue the PKUDOS registry trial to allow enrollment in this study
Pregnant or breastfeeding at screening or planning to become pregnant (self or partner) or breastfeed at any time during the study
Concurrent disease or condition that would interfere with study participation or safety.
Major surgery planned during the study period
Any condition that in the view of the investigator, places the subject at high risk of poor treatment compliance or terminating early from the study
Alanine aminotransferase (ALT) concentration at least 2x the upper limit of normal
Creatinine at least 1.5x the upper limit of normal

For more information on this trial, visit clinicaltrials.gov.