By: Uresti, et al. S.B. No. 450
 
 
 
   
 
A BILL TO BE ENTITLED
AN ACT
relating to enrollment and participation in certain research
programs of certain children in foster care.
       BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:
       SECTION 1.  Section 266.001, Family Code, as added by
Chapter 268, Acts of the 79th Legislature, Regular Session, 2005,
is amended by adding Subdivisions (2-a) and (4-a) to read as
follows:
             (2-a)  "Drug research program" means any clinical
trial, clinical investigation, drug study, or active medical or
clinical research that has been approved by an institutional review
board in accordance with the standards provided in the Code of
Federal Regulations, 45 C.F.R. Sections 46.404 through 46.407,
regarding:
                   (A)  an investigational new drug; or
                   (B)  the efficacy of an approved drug.
             (4-a)  "Investigational new drug" has the meaning
assigned by 21 C.F.R. Section 312.3(b).
       SECTION 2.  Subchapter A, Chapter 266, Family Code, as added
by Chapter 268, Acts of the 79th Legislature, Regular Session,
2005, is amended by adding Section 266.0041 to read as follows:
       Sec. 266.0041.  ENROLLMENT AND PARTICIPATION IN CERTAIN
RESEARCH PROGRAMS.  (a)   Notwithstanding Section 266.004, a person
may not authorize the enrollment of a foster child or consent to the
participation of a foster child in a drug research program without a
court order as provided by this section, unless the person is the
foster child's parent and the person has been authorized by the
court to make medical decisions for the foster child in accordance
with Section 266.004.
       (b)  Before issuing an order authorizing the enrollment or
participation of a foster child in a drug research program, the
court must:
             (1)  appoint an independent medical advocate;
             (2)  review the report filed by the independent medical
advocate regarding the advocate's opinion and recommendations
concerning the foster child's enrollment and participation in the
drug research program;
             (3)  consider whether the person conducting the drug
research program:
                   (A)  informed the foster child in a
developmentally appropriate manner of the expected benefits of the
drug research program, any potential side effects, and any
available alternative treatments and received the foster child's
assent to enroll the child to participate in the drug research
program as required by the Code of Federal Regulations, 45 C.F.R.
Section 46.408; or
                   (B)  received informed consent in accordance with
Subsection (h); and
             (4)  determine whether enrollment and participation in
the drug research program is in the foster child's best interest and
determine that the enrollment and participation in the drug
research program will not interfere with the appropriate medical
care of the foster child.
       (c)  An independent medical advocate appointed under
Subsection (b) is not a party to the suit but may:
             (1)  conduct an investigation regarding the foster
child's participation in a drug research program to the extent that
the advocate considers necessary to determine:
                   (A)  whether the foster child assented to or
provided informed consent to the child's enrollment and
participation in the drug research program; and
                   (B)  the best interest of the child for whom the
advocate is appointed; and
             (2)  obtain and review copies of the foster child's
relevant medical and psychological records and information
describing the risks and benefits of the child's enrollment and
participation in the drug research program.
       (d)  An independent medical advocate shall, within a
reasonable time after the appointment, interview:
             (1)  the foster child in a developmentally appropriate
manner, if the child is four years of age or older;
             (2)  the foster child's parent, if the parent is
entitled to notification under Section 266.005;
             (3)  an advocate appointed by an institutional review
board in accordance with the Code of Federal Regulations, 45 C.F.R.
Section 46.409(b), if an advocate has been appointed;
             (4)  the medical team treating the foster child as well
as the medical team conducting the drug research program; and
             (5)  each individual who has significant knowledge of
the foster child's medical history and condition, including any
foster parent of the child.
       (e)  After reviewing the information collected under
Subsections (c) and (d), the independent medical advocate shall:
             (1)  submit a report to the court presenting the
advocate's opinion and recommendation regarding whether:
                   (A)  the foster child assented to or provided
informed consent to the child's enrollment and participation in the
drug research program; and
                   (B)  the foster child's best interest is served by
enrollment and participation in the drug research program; and
             (2)  at the request of the court, testify regarding the
basis for the advocate's opinion and recommendation concerning the
foster child's enrollment and participation in a drug research
program.
       (f)  The court may appoint any person eligible to serve as
the foster child's guardian ad litem, as defined by Section
107.001, as the independent medical advocate, including a physician
or nurse or an attorney who has experience in medical and health
care, except that a foster parent, employee of a substitute care
provider or child placing agency providing care for the foster
child, representative of the department, medical professional
affiliated with the drug research program, independent medical
advocate appointed by an institutional review board, or any person
the court determines has a conflict of interest may not serve as the
foster child's independent medical advocate.
       (g)  A person otherwise authorized to consent to medical care
for a foster child may petition the court for an order permitting
the enrollment and participation of a foster child in a drug
research program under this section.
       (h)  Before a foster child, who is at least 16 years of age
and has been determined to have the capacity to consent to medical
care in accordance with Section 266.010, may be enrolled to
participate in a drug research program, the person conducting the
drug research program must:
             (1)  inform the foster child in a developmentally
appropriate manner of the expected benefits of participation in the
drug research program, any potential side effects, and any
available alternative treatments; and
             (2)  receive written informed consent to enroll the
foster child for participation in the drug research program.
       (i)  A court may render an order approving the enrollment or
participation of a foster child in a drug research program
involving an investigational new drug before appointing an
independent medical advocate if:
             (1)  a physician recommends the foster child's
enrollment or participation in the drug research program to provide
the foster child with treatment that will prevent the death or
serious injury of the child; and
             (2)  the court determines that the foster child needs
the treatment before an independent medical advocate could complete
an investigation in accordance with this section.
       (j)  As soon as practicable after issuing an order under
Subsection (i), the court shall appoint an independent medical
advocate to complete a full investigation of the foster child's
enrollment and participation in the drug research program in
accordance with this section.
       (k)  This section does not apply to:
             (1)  a drug research study regarding the efficacy of an
approved drug that is based only on medical records, claims data, or
outcome data, including outcome data gathered through interviews
with a child, caregiver of a child, or a child's treating
professional;
             (2)  a retrospective drug research study based only on
medical records, claims data, or outcome data; or
             (3)  the treatment of a foster child with an
investigational new drug that does not require the child's
enrollment or participation in a drug research program.
       (l)  The department shall annually submit to the governor,
lieutenant governor, speaker of the house of representatives, and
the relevant committees in both houses of the legislature, a report
regarding:
             (1)  the number of foster children who enrolled or
participated in a drug research program during the previous year;
             (2)  the purpose of each drug research program in which
a foster child was enrolled or participated; and
             (3)  the number of foster children for whom an order was
issued under Subsection (i).
       SECTION 3.  Subsection (b), Section 266.005, Family Code, as
added by Chapter 268, Acts of the 79th Legislature, Regular
Session, 2005, is amended to read as follows:
       (b)  Except as provided by Subsection (c), the department
shall make reasonable efforts to notify the child's parents within
24 hours of:
             (1)  a significant medical condition involving a foster
child; and
             (2)  the enrollment or participation of a foster child
in a drug research program under Section 266.0041.
       SECTION 4.  The change in law made by this Act by the
enactment of Section 266.0041, Family Code, applies only to the
enrollment and participation of a foster child in a drug research
program on or after the effective date of this Act. A foster child
enrolled or participating in a drug research program before the
effective date of this Act is governed by the law in effect when the
foster child was enrolled or began participating in the drug
research program, and the former law is continued in effect for that
purpose.
       SECTION 5.  This Act takes effect September 1, 2007.