Press Release Prescribing Information
Campath® Alemtuzumab - For Intravenous Use Only
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As a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL) - See Things in a Whole New Light: Campath First Line - Campath® Alemtuzumab For Intravenous Use Only
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CLL Tools and Downloads

This page contains PDF versions of some of the materials found in the Campath Patient Kit. Choose from the links below to download:

Understanding CLL: A Guide for Patients Who Want to Take Charge of Chronic Lymphocytic Leukemia

Here's a comprehensive brochure that summarizes key information about CLL and provides tools for managing treatment.

Download a PDF of Understanding CLL: A Guide for Patients Who Want to Take Charge of Chronic Lymphocytic Leukemia

A Patient-Friendly List of Terms

This tool is a glossary of terms associated with CLL that may help you to better understand your reading about the illness and available treatments.

Download a PDF of A Patient-Friendly List of Terms

Sample Treatment Schedule

You and your doctor will develop a personalized Campath treatment schedule that works best for you. Here's what a treatment schedule looks like.

View a Sample Treatment Schedule

Checklist of Questions To Discuss With Your Doctor

This checklist contains questions to ask your doctor about treatment choices and questions to discuss during your treatment.

View a Checklist of Questions to Discuss With Your Doctor
Indication and Important Safety Information

Campath is indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL).

WARNING: CYTOPENIAS, INFUSION REACTIONS, and INFECTIONS

Cytopenias: Serious, including fatal, pancytopenia/marrow hypoplasia, autoimmune idiopathic thrombocytopenia, and autoimmune hemolytic anemia can occur in patients receiving Campath. Single doses of Campath greater than 30 mg or cumulative doses greater than 90 mg per week increase the incidence of pancytopenia [see WARNINGS AND PRECAUTIONS (5.1)].

Infusion Reactions: Campath administration can result in serious, including fatal, infusion reactions. Carefully monitor patients during infusions and withhold Campath for Grade 3 or 4 infusion reactions. Gradually escalate Campath to the recommended dose at the initiation of therapy and after interruption of therapy for 7 or more days [see DOSAGE AND ADMINISTRATION (2) and WARNINGS AND PRECAUTIONS (5.2)].

Infections: Serious, including fatal, bacterial, viral, fungal, and protozoan infections can occur in patients receiving Campath. Administer prophylaxis against Pneumocystis jiroveci pneumonia (PCP) and herpes virus infections [see DOSAGE AND ADMINISTRATION (2.2) and WARNINGS AND PRECAUTIONS (5.3)].

The most commonly reported adverse reactions are infusion reactions fever, chills, hypotension, urticaria, nausea, rash, tachycardia, dyspnea), cytopenias (neutropenia, lymphopenia, thrombocytopenia, anemia), and infections (CMV viremia, CMV infection, other infections). In clinical trials, the frequency of infusion reactions was highest in the first week of treatment. Other commonly reported adverse reactions include vomiting, abdominal pain, insomnia and anxiety. The most commonly reported serious adverse reactions are cytopenias, infusion reactions, and immunosuppression/infections. See "Warnings and Precautions," and "Adverse Reactions" sections of full Prescribing Information.

Please see Full Prescribing Information (PDF).