CT Insurance Bulletin HC-79
Revised Pre-Authorization Form for Cancer Clinical Trials
Connecticut State Seal
STATE OF CONNECTICUT
INSURANCE DEPARTMENT
BULLETIN He - 79
June 17, 2010
TO:
All Health Insurers and Health Care Centers Authorized To Conduct Business In
Connecticut
RE:
Revised Pre-Authorization Form for Cancer Clinical Trials
This is a reminder to all health insurers and health care centers operating in Connecticut that
pursuant to sections 38a-504f and 38a-542f of the Connecticut General Statutes, and section
38a-504a-3 of the Regulations of the Connecticut State Agencies, all requests for coverage of
routine patient care costs for individuals enrolled in Phase I, II and III cancer clinical trials must
be pre-authorized through a submission of a completed, standardized form that all providers,
hospitals and institutions shall submit when seeking to enroll an insured person in the cancer
clinical trial. The Connecticut Insurance Department ("Department") wants to make sure that the
form is properly required and used to enable proper identification of cancer clinical trial
participants and proper data collection related to benefits provided under the cancer clinical trial
mandates.
Working with representatives of the Connecticut Association of Health Plans, medical directors
and counsel of licensed health care centers, the Attorney General's Office and clinical trial staff
of the Neag Comprehensive Cancer Center of the University of Connecticut, the Department
undertook a review of the cancer clinical trial pre-authorization form to update it. As a result of
that review, the form has been revised and a copy of the revised form is attached for your
information. A copy of the form is also available on the Department's website under "Forms".
Please contact the Insurance Department Life & Health Division at cid.lh@ct.govwith any
questions.
Insurance Commissionner's signature
Insurance Commissioner
www.ct.gov/cid
P.O. Box 816 • Hartford. CT06142-0816
An Equal Opportunity Employer
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Request For Authorization for Coverage of Routine Patient Care Costs
Associated with Cancer Clinical Trials
Section I
Date:
Member name:
Member ID #:
Member Date of Birth:
Health Insurer:
Treating Physician:
_
Contact Person for Additional Information Regarding Member's Treatment:
Name:
Address:
Phone number:
Fax number:
E-mail address:
Service requested is: _Outpatient
_Inpatient _Office Setting
If outpatient or inpatient is checked:
Facility name & address:
_
Please Note: Pursuant to Connecticut General Statutes Sections 38a-504a et seq. (individual
coverage) or 38a-542a et seq. (group coverage), you may be asked to provide additional
information about the cancer clinical trial or the member's diagnosis and condition prior to the
authorization of this request.
CT Insurance Dept - Revised June 2010
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Member name:
Member ID#:
Section II
Diagnosis code:-----Â
Stage
_
Clinical trial phase:
I
II
III
Clinical trial sponsor:
_
Please identify the funding source for the trial? (federal government, private entity, charitable
organization - please provide specific entity name)
_
Clinical Trial has been reviewed and approved by: (must check one per Conn. Gen. Stat. Sec.
38a-504b or 38a-542)
National Institute of Health
National Cancer Institute
_Federal Food and Drug Administration
_Federal Dept. of Defense
_Federal Dept. of Veterans Affairs
Check one: __Single center study
__Multiple center study
List name(s) and addressees) of center(s):
Information regarding the proposed trial: (if additional space is needed for any of the following
questions, please attach separate sheet)
1. Please state the anticipated therapeutic effect
_
2. How does the protocol differ from the standard treatment for this diagnosis?
3. Please provide a list of tests, procedures, drugs, equipment and other services to be covered by
the trial.
4. Please attach copies of the study calendar and schema page from the clinical trial proposal.
CT Insurance Dept - Revised June 20 I0