DOXILine.com - Patient Assistance

PATIENT ASSISTANCE

Welcome

DOXILine Hotline

Tel 1-800-609-1083
Tel 1-800-553-3851 (PROCRITLine analysts can also assist with DOXIL calls)
Fax 1-800-987-5572
Hrs: M-F 9:00 A.M.-8:00 P.M. EST.

DOXILine provides easy access to reimbursement information and support including:

	Benefit Verification
	Prior Authorization research
	Appeal process and procedure research
	Alternate sources of payment
	General billing and coding questions
	Information regarding patient assistance

THE INFORMATION PROVIDED REPRESENTS NO STATEMENT, PROMISE, OR GUARANTEE BY Ortho Biotech Products, L.P. CONCERNING LEVELS OF REIMBURSEMENT. PLEASE CONSULT YOUR PAYER ORGANIZATION WITH REGARD TO LOCAL OR ACTUAL COVERAGE AND REIMBURSEMENT POLICIES AND DETERMINATION PROCESSES.

Patient Assistance Program

Ortho Biotech will provide assistance to certain eligible DOXIL patients at no charge, based on medical and financial need. Our toll-free hotline -- 1-800-609-1083 -- is available Monday through Friday from 9 a.m. to 8 p.m., Eastern Standard Time, to answer questions from patients and health-care providers. Our fax number is 1-800-987-5572.

The toll-free hotline number is convenient and easy to use

When calling about a patient specific reimbursement issue, please have the following information available:

	Selected patient's information
	Name and telephone number of insurance plan(s), policy number(s) and name of subscriber
	Physician's name, address, and telephone number
	Patient's financial information if calling on behalf of an uninsured patient

Patients must authorize disclosure of this information.

Patient Assistance Program Application Form - DOXIL

Click here to view and to print the application for the Patient Assistance Program. This form requires the Adobe Reader for viewing and printing.

Online Registration - Interactive Patient Assistance Program - DOXIL

Click here to submit the Patient Assistance Program Application form electronically. Our new "DOXILine Interactive Patient Assistance Program" will save you time and effort. Once you register, your office and physician data will be saved so that it can be entered automatically for you each time your office submits a form.

Use this feature for the Doxil Patient Assistance Program.

Benefit Verification Form

Click here to view and to print the application for Insurance Benefit Verification for DOXIL. This form requires the Adobe Reader for viewing and printing.

Safety Information

Indications:

DOXIL® (doxorubicin HCl liposome injection) is indicated for the treatment of patients with ovarian cancer whose disease has progressed or recurred after prior platinum-based therapy.
DOXIL in combination with VELCADE® (bortezomib) is indicated for the treatment of patients with multiple myeloma who have not previously received VELCADE and have received at least one prior therapy.
DOXIL is indicated for the treatment of AIDS-related Kaposi's sarcoma in patients with disease that has progressed on prior combination chemotherapy or in patients who are intolerant to such therapy.

The treatment of patients with AIDS-related Kaposi's sarcoma is based on objective tumor response rates. No results are available from controlled trials that demonstrate a clinical benefit resulting from this treatment, such as improvement in disease-related symptoms or increased survival.

IMPORTANT SAFETY INFORMATION

BOXED WARNINGS:
Cardiotoxicity, infusion reaction, myelosuppression, liver impairment, substitution

The use of DOXIL may lead to cardiac toxicity. Myocardial damage may lead to congestive heart failure and may occur as the total cumulative dose of doxorubicin HCl approaches 550mg/m².

Prior use of other anthracyclines or anthracenediones should be included in calculations of total cumulative dose.
Cardiac toxicity may also occur at lower cumulative doses (400 mg/m²) in patients with prior mediastinal irradiation or who are receiving concurrent cyclophosphamide therapy.

Acute infusion-related reactions including, but not limited to, flushing, shortness of breath, facial swelling, headache, chills, back pain, tightness in the chest or throat, and/or hypotension have occurred in up to 10% of patients treated with DOXIL. In most patients, these reactions have resolved within several hours to a day once the infusion is terminated. In some patients, reactions resolved with slowing of the infusion rate.

Serious and sometimes life-threatening or fatal allergic/anaphylactoid-like infusion reactions have occurred. Medications to treat such reactions, as well as emergency equipment, should be available for immediate use.
The initial rate of infusion should be 1mg/min to minimize the risk of infusion reactions.

Severe myelosuppression may occur.
DOXIL dosage should be reduced in patients with impaired hepatic function.
Accidental substitution has resulted in severe side effects. Do not substitute for doxorubicin HCl on a mg per mg basis.

Contraindications

Patients with a history of hypersensitivity reactions to a conventional doxorubicin formulation or the components of DOXIL
Nursing mothers

Additional Safety Information

Cardiac function should be carefully monitored.

Congestive heart failure or cardiomyopathy may occur after discontinuation of anthracycline therapy.
For patients with a history of cardiovascular disease, or if the results of cardiac monitoring indicate possible cardiac injury, the benefit of therapy must be weighed against the risk of myocardial injury.
In the randomized multiple myeloma study, 25 patients (8%) in the VELCADE for Injection arm and 42 patients (13%) in the VELCADE plus DOXIL arm experienced left ventricular ejection fraction decrease (defined as absolute decrease > 15% over baseline or a > 5% decrease below institutional lower limit of normal).

Myelosuppression may occur; frequently monitor complete blood count (including platelet count), at least prior to each dose of DOXIL.

In patients with recurrent ovarian cancer or AIDS-related Kaposi's sarcoma, hematologic toxicity (based on platelet count or absolute neutrophil count) may require dose reduction or delay in administration of DOXIL.
In patients with multiple myeloma, hematologic toxicity (based on platelet count, absolute neutrophil count, hemoglobin level, or neutropenia with fever) may require dose reduction, delay in administration, or suspension of DOXIL and/or VELCADE.
Persistent severe myelosuppression may result in superinfection, neutropenic fever, or hemorrhage.
Sepsis occurring during neutropenia has resulted in discontinuation of treatment and in rare cases of death.

DOXIL may potentiate the toxicity of other anticancer therapies, especially hematologic toxicities, when used in combination with other therapies that suppress bone marrow.
Hand-foot syndrome (HFS) may occur during therapy with DOXIL.

Based on HFS toxicity grade, dose reduction, delay in administration, or discontinuation of DOXIL may be required.
HFS was generally observed after 2 to 3 cycles of treatment, but may occur earlier.

The reaction was mild in most patients, resolving in 1 to 2 weeks.
The reaction can be severe and debilitating in some patients, resulting in discontinuation of therapy.

DOXIL is an irritant, not a vesicant; use precautions to avoid extravasation.
DOXIL can cause fetal harm when used during pregnancy.
Recall reaction has occurred with DOXIL administration after radiotherapy.
DOXIL may interact with drugs known to interact with the conventional formulation of doxorubicin HCl.
In patients with recurrent ovarian cancer, the most common all-grade adverse reactions (ARs) > 20% (DOXIL vs topotecan, respectively) included: asthenia (40% vs 51%), fever (21% vs 31%), nausea (46% vs 63%), stomatitis (41% vs 15%), vomiting (33% vs 44%), diarrhea (21% vs 35%), anorexia (20% vs 22%), dyspnea (15% vs 23%), HFS (51% vs 1%), and rash (29% vs 12%).

In addition, 19% vs 52.3% reported alopecia (all grades).
Grade 3/4 hematologic ARs reported in > 5% (DOXIL vs t opotecan, respectively) were neutropenia (12% vs 76%) and anemia (6% vs 29%).

In patients with multiple myeloma, the most common all-grade ARs > 20% (VELCADE plus DOXIL vs VELCADE, respectively) included: neutropenia (36% vs 22%), thrombocytopenia (33% vs 28%), anemia (25% vs 21%), fatigue (36% vs 28%), pyrexia (31% vs 22%), asthenia (22% vs 18%), nausea (48% vs 40%), diarrhea (46% vs 39%), vomiting (32% vs 22%), constipation (31% vs 31%), mucositis/stomatitis (20% vs 5%), peripheral neuropathy (42% vs 45%), neuralgia (17% vs 20%), and rash (22% vs 18%).

In addition, 19% vs < 1% reported HFS.

In patients with AIDS-related Kaposi's sarcoma, ARs reported in > 5% of DOXIL-treated patients were: neutropenia (ANC < 1000/mm³, 46%; < 500/mm³, 11%), anemia (Hb < 10 g/dL, 58%; < 8 g/dL, 16%), thrombocytopenia (< 150,000 platelets/mm³, 61%), nausea (18%), asthenia (7%), fever (8%), alopecia (9%), vomiting (8%), diarrhea (5%), and stomatitis (5%).

Please see accompanying full Prescribing Information, including Boxed WARNINGS